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Showing metabocard for Digoxin (HMDB0001917)

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Record Information
Version5.0
StatusDetected and Quantified
Creation Date2006-05-18 08:19:31 UTC
Update Date2022-03-07 02:49:11 UTC
HMDB IDHMDB0001917
Secondary Accession Numbers
  • HMDB0014534
  • HMDB01917
  • HMDB14534
Metabolite Identification
Common NameDigoxin
DescriptionDigoxin is a cardiac glycoside extracted from the foxglove plant, digitalis. It is widely used in the treatment of various heart conditions, namely atrial fibrillation, atrial flutter and congestive heart failure that cannot be controlled by other medication. Digoxin preparations are commonly marketed under the trade name Lanoxin. Digoxin has positive inotropic and negative chronotropic activity. It is used to control ventricular rate in atrial fibrillation and in the management of congestive heart failure with atrial fibrillation. Its use in congestive heart failure and sinus rhythm is less certain. The margin between toxic and therapeutic doses is small. (From Martindale, The Extra Pharmacopoeia, 30th ed, p666) -- Pubchem; Digoxin is a cardiotonic glycoside obtained mainly from Digitalis lanata; It consists of three sugars and the aglycone digoxigenin. Digoxin binds to a site on the extracellular aspect of the of the Na+/K+ ATPase pump in the membranes of heart cells (myocytes). This causes an increase in the level of sodium ions in the myocytes, which then leads to a rise in the level of calcium ions. The proposed mechanism is the following: inhibition of the Na+/K+ pump leads to increased Na+ levels, which in turn slows down the extrusion of Ca2+ via the Na+/Ca2+ exchange pump. Increased amounts of Ca2+ are then stored in the sarcoplasmic reticulum and released by each action potential, which is unchanged by digoxin. This is a different mechanism from that of catecholamines. -- Wikipedia ; Owing to its narrow therapeutic index (the margin between effectiveness and toxicity), side effects of digoxin are inevitable. Nausea, vomiting and GIT upset are common, especially in higher doses. Decreased conduction in the AV node can lead to AV blocks, increased intracellular Ca2+ causes a type of arrhythmia called bigeminy (coupled beats), eventually ventricular tachycardia or fibrillation. An often described but rarely seen side effect of digoxin is a disturbance of color vision (mostly yellow and green color) called xanthopsia.
Structure
Data?1582752216
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0001917 (Digoxin)


  Mrv0541 04191212122D          

 58 65  0  0  1  0            999 V2000
   13.3011   -7.7044    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.0047   -7.2489    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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M  END
Download

3D MOL for HMDB0001917 (Digoxin)

HMDB0001917
     RDKit          3D
Digoxin
119126  0  0  0  0  0  0  0  0999 V2000
   11.5191   -0.1291    3.0378 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2419   -0.5402    1.6048 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.3236    0.3399    1.0306 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7743   -0.2615   -0.1155 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.0461    0.6725   -0.8311 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6801    0.4029   -0.7960 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.9419    1.5671   -0.1712 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7565    2.6903   -0.0429 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7638    1.9503   -1.0289 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.3552    0.9387    0.7122 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -5.2926   -0.8466   -1.4072 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.7664    0.0088    1.6894 O   0  0  0  0  0  0  0  0  0  0  0  0
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   10.7544   -0.4981    3.7394 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.5138   -0.5258    3.3165 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.5125    0.9776    3.0570 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8383   -1.5568    1.5846 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0367   -1.0090    0.2912 H   0  0  0  0  0  0  0  0  0  0  0  0
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    6.5215    1.2545    0.8120 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.1203    2.5961   -0.3431 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1253    2.5647   -1.8642 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.8509   -0.9396   -1.0237 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.9892    2.0337    1.3629 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.2189    0.4796    2.7656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6468    1.8568    1.7089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7576   -1.0074    1.8381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5533    0.0178    3.4850 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.3793    2.2778    0.8124 H   0  0  0  0  0  0  0  0  0  0  0  0
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  -10.4087    1.2001   -2.1709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5651   -2.7910    0.3076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8428   -2.1313   -1.3406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4763   -2.3634   -1.4689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2585   -2.2316    0.2982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5401    0.8149   -2.3088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1195    1.0754   -1.2083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1336   -1.7918   -0.8876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7362   -0.9941   -2.3900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2922   -0.7308   -2.1086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2269    0.7555   -2.3348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7188    1.2746   -0.5974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0708   -1.5169    0.5768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8890   -1.0130   -0.6494 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3407    1.3316    1.4785 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1433    1.4288   -0.6436 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8163    2.1575    0.9555 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2177    2.7713   -0.0319 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2466    1.1383   -2.7407 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2642   -1.2407   -3.7521 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3463   -1.6287   -2.3162 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7768   -0.3400   -3.4572 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7757   -2.1073   -0.6700 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6340   -0.8449   -1.9802 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.4390    0.4031   -1.2059 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.5412   -1.2224   -1.9583 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.9235    0.6252    1.0014 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.1590   -1.4918    0.5499 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  6
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  6
 27 29  1  0
 29 30  1  0
 30 31  2  0
 31 32  1  0
 32 33  2  0
 32 34  1  0
 34 35  1  0
 29 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  1  6
 38 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  1  0
 43 44  1  0
 16 45  1  0
 45 46  1  0
 46 47  1  0
 10 48  1  0
 48 49  1  0
 49 50  1  0
  4 51  1  0
 51 52  1  0
 52 53  1  0
 52 54  1  0
 54 55  1  0
 54  2  1  0
 49  6  1  0
 46 12  1  0
 44 18  1  0
 43 21  1  0
 40 23  1  0
 38 27  1  0
 35 30  1  0
  1 56  1  0
  1 57  1  0
  1 58  1  0
  2 59  1  1
  4 60  1  1
  6 61  1  1
  7 62  1  1
  8 63  1  0
  9 64  1  0
  9 65  1  0
 10 66  1  6
 12 67  1  6
 13 68  1  6
 14 69  1  0
 15 70  1  0
 15 71  1  0
 16 72  1  1
 18 73  1  1
 19 74  1  0
 19 75  1  0
 20 76  1  0
 20 77  1  0
 22 78  1  0
 22 79  1  0
 22 80  1  0
 23 81  1  1
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 24 83  1  0
 25 84  1  1
 26 85  1  0
 28 86  1  0
 28 87  1  0
 28 88  1  0
 29 89  1  1
 31 90  1  0
 35 91  1  0
 35 92  1  0
 36 93  1  0
 36 94  1  0
 37 95  1  0
 37 96  1  0
 39 97  1  0
 40 98  1  6
 41 99  1  0
 41100  1  0
 42101  1  0
 42102  1  0
 43103  1  6
 44104  1  0
 44105  1  0
 46106  1  1
 47107  1  0
 47108  1  0
 47109  1  0
 49110  1  6
 50111  1  0
 50112  1  0
 50113  1  0
 51114  1  0
 51115  1  0
 52116  1  6
 53117  1  0
 54118  1  6
 55119  1  0
M  END
Download

3D SDF for HMDB0001917 (Digoxin)


  Mrv0541 04191212122D          

 58 65  0  0  1  0            999 V2000
   13.3011   -7.7044    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.0047   -7.2489    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.7192   -7.6614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4336   -7.2489    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   15.4336   -6.4239    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.7192   -6.0114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0047   -6.4239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1481   -7.6614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8626   -7.2489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8626   -6.4239    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   16.1481   -6.0114    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.5770   -6.0114    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   17.5770   -5.1864    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   16.8626   -4.7739    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   16.1481   -5.1864    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.3616   -6.2663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.8466   -5.5989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.3616   -4.9315    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   18.6204   -4.1342    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.4518   -4.1509    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.7255   -3.3679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.0655   -2.8656    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.3839   -3.3380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.5063   -3.1334    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.5770   -4.3614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.5770   -6.8364    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.8626   -5.5989    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.4336   -5.5989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4336   -8.0739    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   16.1481   -6.8364    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.5632   -7.3271    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.5632   -6.5021    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8487   -6.0896    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.1342   -6.5021    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.1342   -7.3271    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.8487   -7.7396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4197   -6.0896    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7053   -6.5021    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    9.7053   -7.3271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.4197   -7.7396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9908   -6.0896    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2764   -6.5021    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.2764   -7.3271    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.9908   -7.7396    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.5618   -6.0896    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8474   -6.5021    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8474   -7.3271    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.5618   -7.7396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1330   -6.0896    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.4185   -6.5021    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4185   -7.3271    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.1330   -7.7396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7040   -6.0896    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7040   -7.7396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.8485   -5.2533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.9906   -8.5530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1330   -5.2532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8626   -3.9480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  4  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
  5 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 11 15  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 19 23  1  0  0  0  0
 21 24  2  0  0  0  0
 13 25  1  1  0  0  0
 12 26  1  1  0  0  0
 10 27  1  1  0  0  0
  5 28  1  1  0  0  0
  4 29  1  1  0  0  0
 11 30  1  6  0  0  0
 31  1  1  1  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 31 36  1  0  0  0  0
 34 37  1  6  0  0  0
 38 37  1  6  0  0  0
 38 39  1  0  0  0  0
 35 40  1  6  0  0  0
 38 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 39 44  1  0  0  0  0
 42 45  1  1  0  0  0
 46 47  1  0  0  0  0
 47 48  1  1  0  0  0
 43 48  1  1  0  0  0
 46 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 51 52  1  0  0  0  0
 47 52  1  0  0  0  0
 50 53  1  6  0  0  0
 51 54  1  6  0  0  0
 33 55  1  1  0  0  0
 44 56  1  6  0  0  0
 49 57  1  1  0  0  0
 14 58  1  1  0  0  0
M  END
> <DATABASE_ID>
HMDB0001917

> <DATABASE_NAME>
hmdb

> <SMILES>
[H][C@]12CC[C@]3([H])[C@]([H])(C[C@@H](O)[C@]4(C)[C@H](CC[C@]34O)C3=CC(=O)OC3)[C@@]1(C)CC[C@@H](C2)O[C@H]1C[C@H](O)[C@H](O[C@H]2C[C@H](O)[C@H](O[C@H]3C[C@H](O)[C@H](O)[C@@H](C)O3)[C@@H](C)O2)[C@@H](C)O1

> <INCHI_IDENTIFIER>
InChI=1S/C41H64O14/c1-19-36(47)28(42)15-34(50-19)54-38-21(3)52-35(17-30(38)44)55-37-20(2)51-33(16-29(37)43)53-24-8-10-39(4)23(13-24)6-7-26-27(39)14-31(45)40(5)25(9-11-41(26,40)48)22-12-32(46)49-18-22/h12,19-21,23-31,33-38,42-45,47-48H,6-11,13-18H2,1-5H3/t19-,20-,21-,23-,24+,25-,26-,27+,28+,29+,30+,31-,33+,34+,35+,36-,37-,38-,39+,40+,41+/m1/s1

> <INCHI_KEY>
LTMHDMANZUZIPE-PUGKRICDSA-N

> <FORMULA>
C41H64O14

> <MOLECULAR_WEIGHT>
780.9385

> <EXACT_MASS>
780.429606756

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_AVERAGE_POLARIZABILITY>
84.80330180640148

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-[(1S,2S,5S,7R,10R,11S,14R,15S,16R)-5-{[(2R,4S,5S,6R)-5-{[(2S,4S,5S,6R)-5-{[(2S,4S,5S,6R)-4,5-dihydroxy-6-methyloxan-2-yl]oxy}-4-hydroxy-6-methyloxan-2-yl]oxy}-4-hydroxy-6-methyloxan-2-yl]oxy}-11,16-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]-2,5-dihydrofuran-2-one

> <ALOGPS_LOGP>
1.04

> <JCHEM_LOGP>
2.366680672000001

> <ALOGPS_LOGS>
-3.79

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.98355438761116

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.151115824532209

> <JCHEM_PKA_STRONGEST_BASIC>
-2.976075008150179

> <JCHEM_POLAR_SURFACE_AREA>
203.05999999999997

> <JCHEM_REFRACTIVITY>
193.2328

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.27e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
digoxin

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0001917 (Digoxin)

HMDB0001917
     RDKit          3D
Digoxin
119126  0  0  0  0  0  0  0  0999 V2000
   11.5191   -0.1291    3.0378 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2419   -0.5402    1.6048 C   0  0  1  0  0  0  0  0  0  0  0  0
   10.3236    0.3399    1.0306 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.7743   -0.2615   -0.1155 C   0  0  1  0  0  0  0  0  0  0  0  0
    9.0461    0.6725   -0.8311 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6801    0.4029   -0.7960 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.9419    1.5671   -0.1712 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7565    2.6903   -0.0429 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7638    1.9503   -1.0289 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9619    0.7361   -1.4557 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.5230    0.1384   -0.2790 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1410   -0.0045   -0.2257 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7236   -1.4557   -0.1775 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2240   -2.1665    0.8761 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2114   -1.4519   -0.0936 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7342   -0.6324    1.0800 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3004    0.1791    0.6286 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5259   -0.0951    1.2226 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.1354    1.0753    1.9002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6254    0.8723    2.0512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3552    0.9387    0.7122 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.5865    2.4164    0.4545 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6470    0.2069    0.7395 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.6268    0.7680    1.7448 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9342    0.0841    1.6479 C   0  0  1  0  0  0  0  0  0  0  0  0
   -8.8222    0.4788    2.6469 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5594    0.2157    0.2712 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.8971    1.6767    0.0468 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7611   -0.6544    0.2544 C   0  0  1  0  0  0  0  0  0  0  0  0
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    1.7664    0.0088    1.6894 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5264    0.8160    0.8830 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6252    1.8648    0.2551 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7815   -0.1204   -2.1614 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1139    0.1784   -2.1741 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.9224   -0.8391   -2.9600 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7995   -1.0054   -0.9037 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2186   -0.5216   -0.6341 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.0759   -1.5187   -1.1527 O   0  0  0  0  0  0  0  0  0  0  0  0
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   13.4709   -1.3326    1.2629 O   0  0  0  0  0  0  0  0  0  0  0  0
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    0.3426   -1.3653    1.8493 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.9850    1.6959    2.7209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7830   -0.0634    2.5835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7200    2.9413    1.4472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5007    2.6344   -0.1050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6773    2.9029    0.0237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4285   -0.8433    1.0926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2189    0.4796    2.7656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6468    1.8568    1.7089 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7576   -1.0074    1.8381 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5533    0.0178    3.4850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5101    1.9678   -0.9442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3793    2.2778    0.8124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9989    1.8295    0.0723 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0599   -0.8409    1.3306 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.3387   -0.0549    1.1776 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8024   -0.4731   -2.5811 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4087    1.2001   -2.1709 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5651   -2.7910    0.3076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8428   -2.1313   -1.3406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4763   -2.3634   -1.4689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2585   -2.2316    0.2982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5401    0.8149   -2.3088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1195    1.0754   -1.2083 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1336   -1.7918   -0.8876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7362   -0.9941   -2.3900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2922   -0.7308   -2.1086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2269    0.7555   -2.3348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7188    1.2746   -0.5974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0708   -1.5169    0.5768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8890   -1.0130   -0.6494 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3407    1.3316    1.4785 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1433    1.4288   -0.6436 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8163    2.1575    0.9555 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2177    2.7713   -0.0319 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2466    1.1383   -2.7407 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2642   -1.2407   -3.7521 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3463   -1.6287   -2.3162 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.7768   -0.3400   -3.4572 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7757   -2.1073   -0.6700 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6340   -0.8449   -1.9802 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.4390    0.4031   -1.2059 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.5412   -1.2224   -1.9583 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.9235    0.6252    1.0014 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.1590   -1.4918    0.5499 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
Download

PDB for HMDB0001917 (Digoxin)

HEADER    PROTEIN                                 19-APR-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-12         0                                  
HETATM    1  O   UNK     0      24.829 -14.382   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      26.142 -13.531   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      27.476 -14.301   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      28.809 -13.531   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      28.809 -11.991   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      27.476 -11.221   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      26.142 -11.991   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      30.143 -14.301   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      31.477 -13.531   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      31.477 -11.991   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      30.143 -11.221   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      32.810 -11.221   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      32.810  -9.681   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      31.477  -8.911   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      30.143  -9.681   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      34.275 -11.697   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      35.180 -10.451   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      34.275  -9.205   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      34.758  -7.717   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      36.310  -7.748   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      36.821  -6.287   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      35.589  -5.349   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      34.317  -6.231   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      38.278  -5.849   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      32.810  -8.141   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      32.810 -12.761   0.000  0.00  0.00           O+0
HETATM   27  H   UNK     0      31.477 -10.451   0.000  0.00  0.00           H+0
HETATM   28  C   UNK     0      28.809 -10.451   0.000  0.00  0.00           C+0
HETATM   29  H   UNK     0      28.809 -15.071   0.000  0.00  0.00           H+0
HETATM   30  H   UNK     0      30.143 -12.761   0.000  0.00  0.00           H+0
HETATM   31  C   UNK     0      23.451 -13.677   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      23.451 -12.137   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      22.118 -11.367   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      20.784 -12.137   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      20.784 -13.677   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      22.118 -14.447   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      19.450 -11.367   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      18.117 -12.137   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      18.117 -13.677   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      19.450 -14.447   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      16.783 -11.367   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      15.449 -12.137   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      15.449 -13.677   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      16.783 -14.447   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      14.115 -11.367   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0      12.782 -12.137   0.000  0.00  0.00           O+0
HETATM   47  C   UNK     0      12.782 -13.677   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0      14.115 -14.447   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0      11.448 -11.367   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      10.115 -12.137   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      10.115 -13.677   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      11.448 -14.447   0.000  0.00  0.00           C+0
HETATM   53  O   UNK     0       8.781 -11.367   0.000  0.00  0.00           O+0
HETATM   54  O   UNK     0       8.781 -14.447   0.000  0.00  0.00           O+0
HETATM   55  C   UNK     0      22.117  -9.806   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      16.782 -15.966   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0      11.448  -9.806   0.000  0.00  0.00           C+0
HETATM   58  O   UNK     0      31.477  -7.370   0.000  0.00  0.00           O+0
CONECT    1    2   31                                                       
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    8   29                                             
CONECT    5    4    6   11   28                                             
CONECT    6    5    7                                                       
CONECT    7    6    2                                                       
CONECT    8    4    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12   27                                             
CONECT   11   10    5   15   30                                             
CONECT   12   10   13   16   26                                             
CONECT   13   12   14   18   25                                             
CONECT   14   13   15   58                                                  
CONECT   15   14   11                                                       
CONECT   16   12   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   13   19                                                  
CONECT   19   18   20   23                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   24                                                  
CONECT   22   21   23                                                       
CONECT   23   22   19                                                       
CONECT   24   21                                                            
CONECT   25   13                                                            
CONECT   26   12                                                            
CONECT   27   10                                                            
CONECT   28    5                                                            
CONECT   29    4                                                            
CONECT   30   11                                                            
CONECT   31    1   32   36                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34   55                                                  
CONECT   34   33   35   37                                                  
CONECT   35   34   36   40                                                  
CONECT   36   35   31                                                       
CONECT   37   34   38                                                       
CONECT   38   37   39   41                                                  
CONECT   39   38   44                                                       
CONECT   40   35                                                            
CONECT   41   38   42                                                       
CONECT   42   41   43   45                                                  
CONECT   43   42   44   48                                                  
CONECT   44   43   39   56                                                  
CONECT   45   42                                                            
CONECT   46   47   49                                                       
CONECT   47   46   48   52                                                  
CONECT   48   47   43                                                       
CONECT   49   46   50   57                                                  
CONECT   50   49   51   53                                                  
CONECT   51   50   52   54                                                  
CONECT   52   51   47                                                       
CONECT   53   50                                                            
CONECT   54   51                                                            
CONECT   55   33                                                            
CONECT   56   44                                                            
CONECT   57   49                                                            
CONECT   58   14                                                            
MASTER        0    0    0    0    0    0    0    0   58    0  130    0
END
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3D PDB for HMDB0001917 (Digoxin)

COMPND    HMDB0001917
HETATM    1  C1  UNL     1      11.519  -0.129   3.038  1.00  0.00           C  
HETATM    2  C2  UNL     1      11.242  -0.540   1.605  1.00  0.00           C  
HETATM    3  O1  UNL     1      10.324   0.340   1.031  1.00  0.00           O  
HETATM    4  C3  UNL     1       9.774  -0.261  -0.115  1.00  0.00           C  
HETATM    5  O2  UNL     1       9.046   0.672  -0.831  1.00  0.00           O  
HETATM    6  C4  UNL     1       7.680   0.403  -0.796  1.00  0.00           C  
HETATM    7  C5  UNL     1       6.942   1.567  -0.171  1.00  0.00           C  
HETATM    8  O3  UNL     1       7.756   2.690  -0.043  1.00  0.00           O  
HETATM    9  C6  UNL     1       5.764   1.950  -1.029  1.00  0.00           C  
HETATM   10  C7  UNL     1       4.962   0.736  -1.456  1.00  0.00           C  
HETATM   11  O4  UNL     1       4.523   0.138  -0.279  1.00  0.00           O  
HETATM   12  C8  UNL     1       3.141  -0.005  -0.226  1.00  0.00           C  
HETATM   13  C9  UNL     1       2.724  -1.456  -0.178  1.00  0.00           C  
HETATM   14  O5  UNL     1       3.224  -2.167   0.876  1.00  0.00           O  
HETATM   15  C10 UNL     1       1.211  -1.452  -0.094  1.00  0.00           C  
HETATM   16  C11 UNL     1       0.734  -0.632   1.080  1.00  0.00           C  
HETATM   17  O6  UNL     1      -0.300   0.179   0.629  1.00  0.00           O  
HETATM   18  C12 UNL     1      -1.526  -0.095   1.223  1.00  0.00           C  
HETATM   19  C13 UNL     1      -2.135   1.075   1.900  1.00  0.00           C  
HETATM   20  C14 UNL     1      -3.625   0.872   2.051  1.00  0.00           C  
HETATM   21  C15 UNL     1      -4.355   0.939   0.712  1.00  0.00           C  
HETATM   22  C16 UNL     1      -4.587   2.416   0.455  1.00  0.00           C  
HETATM   23  C17 UNL     1      -5.647   0.207   0.739  1.00  0.00           C  
HETATM   24  C18 UNL     1      -6.627   0.768   1.745  1.00  0.00           C  
HETATM   25  C19 UNL     1      -7.934   0.084   1.648  1.00  0.00           C  
HETATM   26  O7  UNL     1      -8.822   0.479   2.647  1.00  0.00           O  
HETATM   27  C20 UNL     1      -8.559   0.216   0.271  1.00  0.00           C  
HETATM   28  C21 UNL     1      -8.897   1.677   0.047  1.00  0.00           C  
HETATM   29  C22 UNL     1      -9.761  -0.654   0.254  1.00  0.00           C  
HETATM   30  C23 UNL     1     -10.941  -0.075  -0.478  1.00  0.00           C  
HETATM   31  C24 UNL     1     -12.084   0.135   0.134  1.00  0.00           C  
HETATM   32  C25 UNL     1     -13.031   0.686  -0.803  1.00  0.00           C  
HETATM   33  O8  UNL     1     -14.248   1.020  -0.562  1.00  0.00           O  
HETATM   34  O9  UNL     1     -12.378   0.787  -2.010  1.00  0.00           O  
HETATM   35  C26 UNL     1     -11.062   0.346  -1.873  1.00  0.00           C  
HETATM   36  C27 UNL     1      -9.332  -1.946  -0.389  1.00  0.00           C  
HETATM   37  C28 UNL     1      -7.808  -1.832  -0.555  1.00  0.00           C  
HETATM   38  C29 UNL     1      -7.617  -0.333  -0.727  1.00  0.00           C  
HETATM   39  O10 UNL     1      -8.053   0.023  -2.017  1.00  0.00           O  
HETATM   40  C30 UNL     1      -6.202   0.112  -0.626  1.00  0.00           C  
HETATM   41  C31 UNL     1      -5.293  -0.847  -1.407  1.00  0.00           C  
HETATM   42  C32 UNL     1      -4.009  -0.049  -1.603  1.00  0.00           C  
HETATM   43  C33 UNL     1      -3.423   0.424  -0.330  1.00  0.00           C  
HETATM   44  C34 UNL     1      -2.498  -0.655   0.206  1.00  0.00           C  
HETATM   45  O11 UNL     1       1.766   0.009   1.689  1.00  0.00           O  
HETATM   46  C35 UNL     1       2.526   0.816   0.883  1.00  0.00           C  
HETATM   47  C36 UNL     1       1.625   1.865   0.255  1.00  0.00           C  
HETATM   48  O12 UNL     1       5.781  -0.120  -2.161  1.00  0.00           O  
HETATM   49  C37 UNL     1       7.114   0.178  -2.174  1.00  0.00           C  
HETATM   50  C38 UNL     1       7.922  -0.839  -2.960  1.00  0.00           C  
HETATM   51  C39 UNL     1      10.799  -1.005  -0.904  1.00  0.00           C  
HETATM   52  C40 UNL     1      12.219  -0.522  -0.634  1.00  0.00           C  
HETATM   53  O13 UNL     1      13.076  -1.519  -1.153  1.00  0.00           O  
HETATM   54  C41 UNL     1      12.534  -0.412   0.828  1.00  0.00           C  
HETATM   55  O14 UNL     1      13.471  -1.333   1.263  1.00  0.00           O  
HETATM   56  H1  UNL     1      10.754  -0.498   3.739  1.00  0.00           H  
HETATM   57  H2  UNL     1      12.514  -0.526   3.317  1.00  0.00           H  
HETATM   58  H3  UNL     1      11.513   0.978   3.057  1.00  0.00           H  
HETATM   59  H4  UNL     1      10.838  -1.557   1.585  1.00  0.00           H  
HETATM   60  H5  UNL     1       9.037  -1.009   0.291  1.00  0.00           H  
HETATM   61  H6  UNL     1       7.475  -0.511  -0.201  1.00  0.00           H  
HETATM   62  H7  UNL     1       6.521   1.255   0.812  1.00  0.00           H  
HETATM   63  H8  UNL     1       7.570   3.187   0.793  1.00  0.00           H  
HETATM   64  H9  UNL     1       5.120   2.596  -0.343  1.00  0.00           H  
HETATM   65  H10 UNL     1       6.125   2.565  -1.864  1.00  0.00           H  
HETATM   66  H11 UNL     1       4.138   0.998  -2.134  1.00  0.00           H  
HETATM   67  H12 UNL     1       2.760   0.403  -1.182  1.00  0.00           H  
HETATM   68  H13 UNL     1       3.012  -1.909  -1.132  1.00  0.00           H  
HETATM   69  H14 UNL     1       4.108  -1.867   1.207  1.00  0.00           H  
HETATM   70  H15 UNL     1       0.790  -2.464  -0.050  1.00  0.00           H  
HETATM   71  H16 UNL     1       0.851  -0.940  -1.024  1.00  0.00           H  
HETATM   72  H17 UNL     1       0.343  -1.365   1.849  1.00  0.00           H  
HETATM   73  H18 UNL     1      -1.366  -0.914   1.958  1.00  0.00           H  
HETATM   74  H19 UNL     1      -1.989   2.034   1.363  1.00  0.00           H  
HETATM   75  H20 UNL     1      -1.746   1.144   2.958  1.00  0.00           H  
HETATM   76  H21 UNL     1      -3.985   1.696   2.721  1.00  0.00           H  
HETATM   77  H22 UNL     1      -3.783  -0.063   2.584  1.00  0.00           H  
HETATM   78  H23 UNL     1      -4.720   2.941   1.447  1.00  0.00           H  
HETATM   79  H24 UNL     1      -5.501   2.634  -0.105  1.00  0.00           H  
HETATM   80  H25 UNL     1      -3.677   2.903   0.024  1.00  0.00           H  
HETATM   81  H26 UNL     1      -5.429  -0.843   1.093  1.00  0.00           H  
HETATM   82  H27 UNL     1      -6.219   0.480   2.766  1.00  0.00           H  
HETATM   83  H28 UNL     1      -6.647   1.857   1.709  1.00  0.00           H  
HETATM   84  H29 UNL     1      -7.758  -1.007   1.838  1.00  0.00           H  
HETATM   85  H30 UNL     1      -8.553   0.018   3.485  1.00  0.00           H  
HETATM   86  H31 UNL     1      -8.510   1.968  -0.944  1.00  0.00           H  
HETATM   87  H32 UNL     1      -8.379   2.278   0.812  1.00  0.00           H  
HETATM   88  H33 UNL     1      -9.999   1.830   0.072  1.00  0.00           H  
HETATM   89  H34 UNL     1     -10.060  -0.841   1.331  1.00  0.00           H  
HETATM   90  H35 UNL     1     -12.339  -0.055   1.178  1.00  0.00           H  
HETATM   91  H36 UNL     1     -10.802  -0.473  -2.581  1.00  0.00           H  
HETATM   92  H37 UNL     1     -10.409   1.200  -2.171  1.00  0.00           H  
HETATM   93  H38 UNL     1      -9.565  -2.791   0.308  1.00  0.00           H  
HETATM   94  H39 UNL     1      -9.843  -2.131  -1.341  1.00  0.00           H  
HETATM   95  H40 UNL     1      -7.476  -2.363  -1.469  1.00  0.00           H  
HETATM   96  H41 UNL     1      -7.259  -2.232   0.298  1.00  0.00           H  
HETATM   97  H42 UNL     1      -7.540   0.815  -2.309  1.00  0.00           H  
HETATM   98  H43 UNL     1      -6.120   1.075  -1.208  1.00  0.00           H  
HETATM   99  H44 UNL     1      -5.134  -1.792  -0.888  1.00  0.00           H  
HETATM  100  H45 UNL     1      -5.736  -0.994  -2.390  1.00  0.00           H  
HETATM  101  H46 UNL     1      -3.292  -0.731  -2.109  1.00  0.00           H  
HETATM  102  H47 UNL     1      -4.227   0.756  -2.335  1.00  0.00           H  
HETATM  103  H48 UNL     1      -2.719   1.275  -0.597  1.00  0.00           H  
HETATM  104  H49 UNL     1      -3.071  -1.517   0.577  1.00  0.00           H  
HETATM  105  H50 UNL     1      -1.889  -1.013  -0.649  1.00  0.00           H  
HETATM  106  H51 UNL     1       3.341   1.332   1.479  1.00  0.00           H  
HETATM  107  H52 UNL     1       1.143   1.429  -0.644  1.00  0.00           H  
HETATM  108  H53 UNL     1       0.816   2.157   0.955  1.00  0.00           H  
HETATM  109  H54 UNL     1       2.218   2.771  -0.032  1.00  0.00           H  
HETATM  110  H55 UNL     1       7.247   1.138  -2.741  1.00  0.00           H  
HETATM  111  H56 UNL     1       7.264  -1.241  -3.752  1.00  0.00           H  
HETATM  112  H57 UNL     1       8.346  -1.629  -2.316  1.00  0.00           H  
HETATM  113  H58 UNL     1       8.777  -0.340  -3.457  1.00  0.00           H  
HETATM  114  H59 UNL     1      10.776  -2.107  -0.670  1.00  0.00           H  
HETATM  115  H60 UNL     1      10.634  -0.845  -1.980  1.00  0.00           H  
HETATM  116  H61 UNL     1      12.439   0.403  -1.206  1.00  0.00           H  
HETATM  117  H62 UNL     1      13.541  -1.222  -1.958  1.00  0.00           H  
HETATM  118  H63 UNL     1      12.923   0.625   1.001  1.00  0.00           H  
HETATM  119  H64 UNL     1      14.159  -1.492   0.550  1.00  0.00           H  
CONECT    1    2   56   57   58
CONECT    2    3   54   59
CONECT    3    4
CONECT    4    5   51   60
CONECT    5    6
CONECT    6    7   49   61
CONECT    7    8    9   62
CONECT    8   63
CONECT    9   10   64   65
CONECT   10   11   48   66
CONECT   11   12
CONECT   12   13   46   67
CONECT   13   14   15   68
CONECT   14   69
CONECT   15   16   70   71
CONECT   16   17   45   72
CONECT   17   18
CONECT   18   19   44   73
CONECT   19   20   74   75
CONECT   20   21   76   77
CONECT   21   22   23   43
CONECT   22   78   79   80
CONECT   23   24   40   81
CONECT   24   25   82   83
CONECT   25   26   27   84
CONECT   26   85
CONECT   27   28   29   38
CONECT   28   86   87   88
CONECT   29   30   36   89
CONECT   30   31   31   35
CONECT   31   32   90
CONECT   32   33   33   34
CONECT   34   35
CONECT   35   91   92
CONECT   36   37   93   94
CONECT   37   38   95   96
CONECT   38   39   40
CONECT   39   97
CONECT   40   41   98
CONECT   41   42   99  100
CONECT   42   43  101  102
CONECT   43   44  103
CONECT   44  104  105
CONECT   45   46
CONECT   46   47  106
CONECT   47  107  108  109
CONECT   48   49
CONECT   49   50  110
CONECT   50  111  112  113
CONECT   51   52  114  115
CONECT   52   53   54  116
CONECT   53  117
CONECT   54   55  118
CONECT   55  119
END
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SMILES for HMDB0001917 (Digoxin)

[H][C@]12CC[C@]3([H])[C@]([H])(C[C@@H](O)[C@]4(C)[C@H](CC[C@]34O)C3=CC(=O)OC3)[C@@]1(C)CC[C@@H](C2)O[C@H]1C[C@H](O)[C@H](O[C@H]2C[C@H](O)[C@H](O[C@H]3C[C@H](O)[C@H](O)[C@@H](C)O3)[C@@H](C)O2)[C@@H](C)O1
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INCHI for HMDB0001917 (Digoxin)

InChI=1S/C41H64O14/c1-19-36(47)28(42)15-34(50-19)54-38-21(3)52-35(17-30(38)44)55-37-20(2)51-33(16-29(37)43)53-24-8-10-39(4)23(13-24)6-7-26-27(39)14-31(45)40(5)25(9-11-41(26,40)48)22-12-32(46)49-18-22/h12,19-21,23-31,33-38,42-45,47-48H,6-11,13-18H2,1-5H3/t19-,20-,21-,23-,24+,25-,26-,27+,28+,29+,30+,31-,33+,34+,35+,36-,37-,38-,39+,40+,41+/m1/s1
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View in JSmolView Stereo Labels
Synonyms
ValueSource
12beta-HydroxydigitoxinChEBI
LanoxicapsKegg
LanoxinKegg
12b-HydroxydigitoxinGenerator
12Β-hydroxydigitoxinGenerator
CardoxinHMDB
CogoxinHMDB
DavoxinHMDB
DigacinHMDB
Digitalis glycosideHMDB
Digoxin pediatricHMDB
DilanacinHMDB
DynamosHMDB
EudigoxHMDB
Homolle'S digitalinHMDB
LanacristHMDB
LanicorHMDB
Neo-lanicorHMDB
RougoxinHMDB
SK-DigoxinHMDB
VanoxinHMDB
AWD.pharma brand OF digoxinHMDB
Boehringer, digoxinaHMDB
Hemigoxine nativelleHMDB
Nativelle, hemigoxineHMDB
Novartis brand OF digoxinHMDB
Roche brand OF digoxinHMDB
Teofarma brand OF digoxinHMDB
Lanoxin PGHMDB
Lanoxin-PGHMDB
R.A.N. brand OF digoxinHMDB
DigoregenHMDB
Digoxina boehringerHMDB
Kern brand OF digoxinHMDB
LanacordinHMDB
Lilly brand OF digoxinHMDB
MapluxinHMDB
Proctor and gamble brand OF digoxinHMDB
UDL brand OF digoxinHMDB
Virco brand OF digoxinHMDB
Bertek brand OF digoxinHMDB
DigitekHMDB
Digoxine nativelleHMDB
Glaxo wellcome brand OF digoxinHMDB
GlaxoSmithKline brand 1 OF digoxinHMDB
GlaxoSmithKline brand 2 OF digoxinHMDB
LenoxinHMDB
Nativelle, digoxineHMDB
Chemical FormulaC41H64O14
Average Molecular Weight780.9385
Monoisotopic Molecular Weight780.429606756
IUPAC Name4-[(1S,2S,5S,7R,10R,11S,14R,15S,16R)-5-{[(2R,4S,5S,6R)-5-{[(2S,4S,5S,6R)-5-{[(2S,4S,5S,6R)-4,5-dihydroxy-6-methyloxan-2-yl]oxy}-4-hydroxy-6-methyloxan-2-yl]oxy}-4-hydroxy-6-methyloxan-2-yl]oxy}-11,16-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]-2,5-dihydrofuran-2-one
Traditional Namedigoxin
CAS Registry Number20830-75-5
SMILES
[H][C@]12CC[C@]3([H])[C@]([H])(C[C@@H](O)[C@]4(C)[C@H](CC[C@]34O)C3=CC(=O)OC3)[C@@]1(C)CC[C@@H](C2)O[C@H]1C[C@H](O)[C@H](O[C@H]2C[C@H](O)[C@H](O[C@H]3C[C@H](O)[C@H](O)[C@@H](C)O3)[C@@H](C)O2)[C@@H](C)O1
InChI Identifier
InChI=1S/C41H64O14/c1-19-36(47)28(42)15-34(50-19)54-38-21(3)52-35(17-30(38)44)55-37-20(2)51-33(16-29(37)43)53-24-8-10-39(4)23(13-24)6-7-26-27(39)14-31(45)40(5)25(9-11-41(26,40)48)22-12-32(46)49-18-22/h12,19-21,23-31,33-38,42-45,47-48H,6-11,13-18H2,1-5H3/t19-,20-,21-,23-,24+,25-,26-,27+,28+,29+,30+,31-,33+,34+,35+,36-,37-,38-,39+,40+,41+/m1/s1
InChI KeyLTMHDMANZUZIPE-PUGKRICDSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as cardenolide glycosides and derivatives. Cardenolide glycosides and derivatives are compounds containing a carbohydrate glycosidically bound to the cardenolide moiety.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassSteroids and steroid derivatives
Sub ClassSteroid lactones
Direct ParentCardenolide glycosides and derivatives
Alternative Parents
Substituents
  • Cardanolide-glycoside
  • Steroidal glycoside
  • Oligosaccharide
  • 12-hydroxysteroid
  • 14-hydroxysteroid
  • Hydroxysteroid
  • Glycosyl compound
  • O-glycosyl compound
  • 2-furanone
  • Oxane
  • Cyclic alcohol
  • Dihydrofuran
  • Alpha,beta-unsaturated carboxylic ester
  • Enoate ester
  • Tertiary alcohol
  • Lactone
  • Carboxylic acid ester
  • Secondary alcohol
  • Organoheterocyclic compound
  • Oxacycle
  • Acetal
  • Carboxylic acid derivative
  • Monocarboxylic acid or derivatives
  • Hydrocarbon derivative
  • Alcohol
  • Organic oxide
  • Organic oxygen compound
  • Carbonyl group
  • Organooxygen compound
  • Aliphatic heteropolycyclic compound
Molecular FrameworkAliphatic heteropolycyclic compounds
External Descriptors
Ontology
Physiological effectNot Available
Disposition
Biological location
ProcessNot Available
Role
Industrial applicationBiological role
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point249 °CNot Available
Boiling Point931.60 °C. @ 760.00 mm Hg (est)The Good Scents Company Information System
Water Solubility0.065 mg/mL at 25 °CNot Available
LogP1.26SANGSTER (1993)
Experimental Chromatographic Properties

Experimental Collision Cross Sections

Adduct TypeData SourceCCS Value (Å2)Reference
[M+H]+Not Available322.483http://allccs.zhulab.cn/database/detail?ID=AllCCS00001515
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.13 g/LALOGPS
logP1.04ALOGPS
logP2.37ChemAxon
logS-3.8ALOGPS
pKa (Strongest Acidic)7.15ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count13ChemAxon
Hydrogen Donor Count6ChemAxon
Polar Surface Area203.06 ŲChemAxon
Rotatable Bond Count7ChemAxon
Refractivity193.23 m³·mol⁻¹ChemAxon
Polarizability84.8 ųChemAxon
Number of Rings8ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleYesChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
AllCCS[M+H]+268.14532859911
AllCCS[M-H]-239.95932859911
DeepCCS[M-2H]-296.50530932474
DeepCCS[M+Na]+270.28230932474
AllCCS[M+H]+268.132859911
AllCCS[M+H-H2O]+268.332859911
AllCCS[M+NH4]+267.932859911
AllCCS[M+Na]+267.832859911
AllCCS[M-H]-240.032859911
AllCCS[M+Na-2H]-245.132859911
AllCCS[M+HCOO]-250.932859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Digoxin[H][C@]12CC[C@]3([H])[C@]([H])(C[C@@H](O)[C@]4(C)[C@H](CC[C@]34O)C3=CC(=O)OC3)[C@@]1(C)CC[C@@H](C2)O[C@H]1C[C@H](O)[C@H](O[C@H]2C[C@H](O)[C@H](O[C@H]3C[C@H](O)[C@H](O)[C@@H](C)O3)[C@@H](C)O2)[C@@H](C)O14569.4Standard polar33892256
Digoxin[H][C@]12CC[C@]3([H])[C@]([H])(C[C@@H](O)[C@]4(C)[C@H](CC[C@]34O)C3=CC(=O)OC3)[C@@]1(C)CC[C@@H](C2)O[C@H]1C[C@H](O)[C@H](O[C@H]2C[C@H](O)[C@H](O[C@H]3C[C@H](O)[C@H](O)[C@@H](C)O3)[C@@H](C)O2)[C@@H](C)O15716.6Standard non polar33892256
Digoxin[H][C@]12CC[C@]3([H])[C@]([H])(C[C@@H](O)[C@]4(C)[C@H](CC[C@]34O)C3=CC(=O)OC3)[C@@]1(C)CC[C@@H](C2)O[C@H]1C[C@H](O)[C@H](O[C@H]2C[C@H](O)[C@H](O[C@H]3C[C@H](O)[C@H](O)[C@@H](C)O3)[C@@H](C)O2)[C@@H](C)O16249.8Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Digoxin GC-MS (TMS_1_1) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Digoxin GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Digoxin GC-MS (TMS_1_3) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Digoxin GC-MS (TMS_1_4) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Digoxin GC-MS (TMS_1_5) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Digoxin GC-MS (TMS_1_6) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Digoxin GC-MS (TBDMS_1_1) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Digoxin GC-MS (TBDMS_1_2) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Digoxin GC-MS (TBDMS_1_3) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Digoxin GC-MS (TBDMS_1_4) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Digoxin GC-MS (TBDMS_1_5) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Digoxin GC-MS (TBDMS_1_6) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Digoxin 10V, Positive-QTOFsplash10-0h9s-0004022900-fb7295b1343cfcb0f2622016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Digoxin 20V, Positive-QTOFsplash10-00ec-0209043100-9967a858c77340d2fab32016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Digoxin 40V, Positive-QTOFsplash10-007o-1419132100-e5de5e30c4299c9316712016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Digoxin 10V, Negative-QTOFsplash10-01tj-0114011900-e0edd63658065bb869f32016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Digoxin 20V, Negative-QTOFsplash10-01bj-2519564400-bd5189ac4cf921dbac792016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Digoxin 40V, Negative-QTOFsplash10-014i-6105930000-b03a6876fb182cec49e12016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Digoxin 10V, Positive-QTOFsplash10-01q9-0113000900-5c07bff161d1ddd9c50e2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Digoxin 20V, Positive-QTOFsplash10-01q9-2911000400-fe987c159da70447f56d2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Digoxin 40V, Positive-QTOFsplash10-005a-6942010000-377898578023a42020d52021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Digoxin 10V, Negative-QTOFsplash10-00os-0501095500-c884ce473f948cad43ce2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Digoxin 20V, Negative-QTOFsplash10-004i-4900011400-932fc5fee2cbc1e58a5a2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Digoxin 40V, Negative-QTOFsplash10-004l-5900001400-b3251bf0b534b08a8db82021-09-22Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Extracellular
  • Membrane
Biospecimen Locations
  • Blood
Tissue Locations
  • Brain
  • Intestine
  • Kidney
  • Liver
  • Platelet
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected and Quantified0.0007 +/- 0.00007 uMAdult (>18 years old)BothNormal details
Abnormal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected and Quantified0.0014 +/- 0.0001 uMAdult (>18 years old)BothHeart failure details
Predicted Concentrations
BiospecimenValueOriginal ageOriginal sexOriginal conditionComments
Blood0.000 umol/mmol creatinineAdult (>18 years old)BothNormalPredicted based on drug qualities
Associated Disorders and Diseases
Disease References
Heart failure
  1. Adams KF Jr, Gheorghiade M, Uretsky BF, Patterson JH, Schwartz TA, Young JB: Clinical benefits of low serum digoxin concentrations in heart failure. J Am Coll Cardiol. 2002 Mar 20;39(6):946-53. [PubMed:11897434 ]
Associated OMIM IDsNone
DrugBank IDDB00390
Phenol Explorer Compound IDNot Available
FooDB IDFDB022736
KNApSAcK IDC00003618
Chemspider ID2006532
KEGG Compound IDC06956
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkDigoxin
METLIN ID2047
PubChem Compound2724385
PDB IDNot Available
ChEBI ID4551
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDMDB00000357
Good Scents IDrw1133251
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Download (PDF)
General References
  1. Mikkaichi T, Suzuki T, Onogawa T, Tanemoto M, Mizutamari H, Okada M, Chaki T, Masuda S, Tokui T, Eto N, Abe M, Satoh F, Unno M, Hishinuma T, Inui K, Ito S, Goto J, Abe T: Isolation and characterization of a digoxin transporter and its rat homologue expressed in the kidney. Proc Natl Acad Sci U S A. 2004 Mar 9;101(10):3569-74. Epub 2004 Mar 1. [PubMed:14993604 ]
  2. Bachmakov I, Rekersbrink S, Hofmann U, Eichelbaum M, Fromm MF: Characterisation of (R/S)-propafenone and its metabolites as substrates and inhibitors of P-glycoprotein. Naunyn Schmiedebergs Arch Pharmacol. 2005 Mar;371(3):195-201. Epub 2005 Apr 15. [PubMed:15900513 ]
  3. Kurup RK, Kurup PA: Hypothalamic digoxin and isoprenoid pathway dysfunction relation to alcoholic addiction, alcoholic cirrhosis, and acquired hepatocerebral degeneration--relation to hemispheric chemical dominance. Int J Neurosci. 2003 Apr;113(4):547-63. [PubMed:12856482 ]
  4. Weber P, Lettieri JT, Kaiser L, Mazzu AL: Lack of mutual pharmacokinetic interaction between cerivastatin, a new HMG-CoA reductase inhibitor, and digoxin in healthy normocholesterolemic volunteers. Clin Ther. 1999 Sep;21(9):1563-75. [PubMed:10509851 ]
  5. Pahkla R, Irs A, Oselin K, Rootslane L: Digoxin: use pattern in Estonia and bioavailability of the local market leader. J Clin Pharm Ther. 1999 Oct;24(5):375-80. [PubMed:10583701 ]
  6. Jablecka A, Chmara E, Korzeniowska K: The level of plasma neuroendocrine activity and the concentration of digoxin in the serum of patients with mild chronic heart failure. Int J Clin Pharmacol Res. 1998;18(4):171-8. [PubMed:10052027 ]
  7. Kurup RK, Kurup PA: Hypothalamic digoxin and hemispheric chemical dominance: relation to alcoholic addiction, alcoholic cirrhosis, and acquired hepatocerebral degeneration. Int J Neurosci. 2003 Aug;113(8):1105-25. [PubMed:12888425 ]
  8. Chirinos JA, Castrellon A, Zambrano JP, Jimenez JJ, Jy W, Horstman LL, Willens HJ, Castellanos A, Myerburg RJ, Ahn YS: Digoxin use is associated with increased platelet and endothelial cell activation in patients with nonvalvular atrial fibrillation. Heart Rhythm. 2005 May;2(5):525-9. [PubMed:15840479 ]
  9. Dasgupta A, Trejo O: Suppression of total digoxin concentrations by digoxin-like immunoreactive substances in the MEIA digoxin assay. Elimination of negative interference by monitoring free digoxin concentrations. Am J Clin Pathol. 1999 Mar;111(3):406-10. [PubMed:10078117 ]
  10. Ravikumar A, Kurup PA: The isoprenoid pathway in lone atrial fibrillation with embolic stroke. Indian Heart J. 2001 Mar-Apr;53(2):184-8. [PubMed:11428474 ]
  11. Cuena Boy R, Martin Montero Mdel P: [Digoxin dosing in the aged: new pharmacokinetic system versus Jellife and Koup methods]. Invest Clin. 2003 Mar;44(1):31-9. [PubMed:12703181 ]
  12. Bentur Y, Tsipiniuk A, Taitelman U: Postmortem digoxin-like immunoreactive substances (DLIS) in patients not treated with digoxin. Hum Exp Toxicol. 1999 Feb;18(2):67-70. [PubMed:10100017 ]
  13. Johnson RD, Dorr MB, Hunt TL, Conway S, Talbot GH: Pharmacokinetic interaction of sparfloxacin and digoxin. Clin Ther. 1999 Feb;21(2):368-79. [PubMed:10211539 ]
  14. Mrozikiewicz A: Endogenous drug-like factors. Pol J Pharmacol. 1998 Nov-Dec;50(6):393-7. [PubMed:10385921 ]
  15. Peters J, Welker HA, Bullingham R: Pharmacokinetic and pharmacodynamic aspects of concomitant mibefradil-digoxin therapy at therapeutic doses. Eur J Drug Metab Pharmacokinet. 1999 Apr-Jun;24(2):133-40. [PubMed:10510740 ]
  16. Cuena Boy R, Ortiz de Apodaca Ruiz MA, Macia Martinez MA: [Best result of digoxin dosing in the aged by taking into account that both the elimination as well as the volume of distribution of the drug decrease when the kidney function deteriorates]. An Med Interna. 2002 Jul;19(7):331-5. [PubMed:12224140 ]
  17. Kurup RK, Kurup PA: Hypothalamic digoxin, hemispheric chemical dominance, and inflammatory bowel disease. Int J Neurosci. 2003 Sep;113(9):1221-40. [PubMed:12959741 ]
  18. Doering W, Konig E, Sturm W: [Digitalis intoxication: specifity and significance of cardiac and extracardiac symptoms. part I: Patients with digitalis-induced arrhythmias (author's transl)]. Z Kardiol. 1977 Mar;66(3):121-8. [PubMed:857452 ]
  19. Kaplanski J, Weinhouse E, Topaz M, Genchik G: Verapamil and digoxin: interactions in the rat. Res Commun Chem Pathol Pharmacol. 1983 Dec;42(3):377-88. [PubMed:6665298 ]
  20. Thompson DF, Carter JR: Drug-induced gynecomastia. Pharmacotherapy. 1993 Jan-Feb;13(1):37-45. [PubMed:8094898 ]
  21. Flanagan RJ, Jones AL: Fab antibody fragments: some applications in clinical toxicology. Drug Saf. 2004;27(14):1115-33. [PubMed:15554746 ]

Enzymes

Enzyme Details
1. Cholesterol side-chain cleavage enzyme, mitochondrial
General function:
Involved in monooxygenase activity
Specific function:
Catalyzes the side-chain cleavage reaction of cholesterol to pregnenolone.
Gene Name:
CYP11A1
Uniprot ID:
P05108
Molecular weight:
60101.87
Enzyme Details
2. Sodium/potassium-transporting ATPase subunit alpha-1
General function:
Involved in ATP binding
Specific function:
This is the catalytic component of the active enzyme, which catalyzes the hydrolysis of ATP coupled with the exchange of sodium and potassium ions across the plasma membrane. This action creates the electrochemical gradient of sodium and potassium ions, providing the energy for active transport of various nutrients.
Gene Name:
ATP1A1
Uniprot ID:
P05023
Molecular weight:
112895.01

Transporters

Enzyme Details
1. Solute carrier organic anion transporter family member 1B1
General function:
Involved in transporter activity
Specific function:
Mediates the Na(+)-independent transport of organic anions such as pravastatin, taurocholate, methotrexate, dehydroepiandrosterone sulfate, 17-beta-glucuronosyl estradiol, estrone sulfate, prostaglandin E2, thromboxane B2, leukotriene C3, leukotriene E4, thyroxine and triiodothyronine. May play an important role in the clearance of bile acids and organic anions from the liver
Gene Name:
SLCO1B1
Uniprot ID:
Q9Y6L6
Molecular weight:
76448.0
Enzyme Details
2. Solute carrier organic anion transporter family member 4C1
General function:
Involved in transporter activity
Specific function:
Organic anion transporter, capable of transporting pharmacological substances such as digoxin, ouabain, thyroxine, methotrexate and cAMP. May participate in the regulation of membrane transport of ouabain. Involved in the uptake of the dipeptidyl peptidase-4 inhibitor sitagliptin and hence may play a role in its transport into and out of renal proximal tubule cells. May be involved in the first step of the transport pathway of digoxin and various compounds into the urine in the kidney. May be involved in sperm maturation by enabling directed movement of organic anions and compounds within or between cells. This ion- transporting process is important to maintain the strict epididymal homeostasis necessary for sperm maturation. May have a role in secretory functions since seminal vesicle epithelial cells are assumed to secrete proteins involved in decapacitation by modifying surface proteins to facilitate the acquisition of the ability to fertilize the egg
Gene Name:
SLCO4C1
Uniprot ID:
Q6ZQN7
Molecular weight:
78947.5