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Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References enzymes (2) Show 2 proteins XML

Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2012-09-11 17:34:11 UTC

Update Date

2022-03-07 02:52:23 UTC

HMDB ID

HMDB0030017

Secondary Accession Numbers

HMDB30017

Metabolite Identification

Common Name

Menatetrenone

Description

Menatetrenone, also known as MK-4, is a vitamin K compound used as a hemostatic agent, and also as adjunctive therapy for the pain of osteoporosis. Menatetrenone is one of the nine forms of vitamin K2 and is a short-chain menaquinone. MK-4 is produced via conversion of vitamin K1 in the body, in the testes, pancreas and arterial walls (Wikipedia ). Vitamin K2 is found in brassicas. Vitamin K2 is widely distributed in green leaves and vegetables. It is a fat-soluble dietary factor effective in controlling blood coagulation. All members of the vitamin K group of vitamins share a methylated naphthoquinone ring structure and vary in the aliphatic side chain attached at the 3-position. Phylloquinone (also known as vitamin K1) invariably contains in its side chain four isoprenoid residues, one of which is unsaturated. Human milk contains between 1 and 4 micrograms/litre of vitamin K1, while formula-derived milk can contain up to 100 micrograms/litre in supplemented formulas. Vitamin K2 concentrations in human milk appear to be much lower than those of vitamin K1. It is estimated that there is a 0.25 to 1.7 percent occurrence of vitamin K deficiency bleeding in the first week of the infant's life with a prevalence of 2-10 cases per 100,000 births. The biochemistry of how vitamin K is used to convert glutamic acid (Glu) to gamma-carboxyglutamic acid (Gla) has been elucidated over the past thirty years in academic laboratories throughout the world. Within the cell, vitamin K undergoes electron reduction to a reduced form of vitamin K (called vitamin K hydroquinone) by the enzyme vitamin K epoxide reductase (or VKOR). Another enzyme then oxidizes vitamin K hydroquinone to allow carboxylation of Glu to Gla; this enzyme is called the gamma-glutamyl carboxylase or the vitamin K-dependent carboxylase. The carboxylation reaction will only proceed if the carboxylase enzyme is able to oxidize vitamin K hydroquinone to vitamin K epoxide at the same time. The carboxylation and epoxidation reactions are said to be coupled reactions. Vitamin K epoxide is then re-converted into vitamin K by the vitamin K epoxide reductase. These two enzymes comprise the so-called vitamin K cycle. Vitamin K2 is one of the reasons why vitamin K is rarely deficient in a human diet (vitamin K is continually recycled in our cells). Vitamin K1 is also known as phylloquinone or phytomenadione (also called phytonadione). Vitamin K2 (menaquinone, menatetrenone) is normally produced by bacteria in the large intestine, and dietary deficiency is extremely rare unless the intestines are heavily damaged or are unable to absorb the molecule, or due to decreased production by normal flora, as seen in broad spectrum antibiotic use.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv1652306301800182D          

 36 37  0  0  0  0            999 V2000
    9.2881   11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    9.4875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    8.6625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    6.1875    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    3.7125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  2  0  0  0  0
 12  9  1  0  0  0  0
 13  9  1  0  0  0  0
 14 10  1  0  0  0  0
 15 10  1  0  0  0  0
 16 11  1  0  0  0  0
 17 11  1  0  0  0  0
 18  7  1  0  0  0  0
 19  8  1  0  0  0  0
 21 20  1  0  0  0  0
 22  1  1  0  0  0  0
 22  2  1  0  0  0  0
 22 12  2  0  0  0  0
 23  3  1  0  0  0  0
 23 13  1  0  0  0  0
 23 14  2  0  0  0  0
 24  4  1  0  0  0  0
 24 15  1  0  0  0  0
 24 16  2  0  0  0  0
 25  5  1  0  0  0  0
 25 17  1  0  0  0  0
 25 20  2  0  0  0  0
 26  6  1  0  0  0  0
 27 21  1  0  0  0  0
 27 26  2  0  0  0  0
 28 18  2  0  0  0  0
 29 19  2  0  0  0  0
 29 28  1  0  0  0  0
 30 26  1  0  0  0  0
 30 28  1  0  0  0  0
 31 27  1  0  0  0  0
 31 29  1  0  0  0  0
 32 30  2  0  0  0  0
 33 31  2  0  0  0  0
 34 14  1  0  0  0  0
 35 16  1  0  0  0  0
 36 20  1  0  0  0  0
M  END

HMDB0030017
     RDKit          3D
Menatetrenone
 73 74  0  0  0  0  0  0  0  0999 V2000
   -9.4523   -0.3062   -1.3208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5857    0.1989   -0.2154 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6441   -0.4797    1.0813 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8004    1.2349   -0.4433 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.4458    1.7756    0.0925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9856    0.3906   -0.1397 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9530   -0.6532    0.9014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5662    0.0360   -1.3653 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0980   -1.3140   -1.6671 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6651   -1.3548   -2.1361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6861   -0.8442   -1.1679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7203    0.5528   -0.6797 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7198   -1.6692   -0.7170 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3085   -1.2441    0.2586 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.7727   -1.5816    2.0878 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4795    0.1310    0.5472 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4588    0.6428    1.5153 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8483    0.6211    0.9916 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8339   -0.0305    1.5770 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6095   -0.8004    2.8261 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1985   -0.0311    1.0296 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1425   -0.6584    1.5950 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5400    0.6882   -0.1907 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8323    0.6722   -0.6859 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1163    1.3581   -1.8329 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1220    2.0535   -2.4806 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8262    2.0619   -1.9726 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5213    1.3749   -0.8154 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1802    1.3550   -0.2468 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2657    1.9866   -0.8306 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9423   -0.3055   -2.2889 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3153    0.4133   -1.4120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9094   -1.2847   -1.0790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6550   -0.9720    1.1882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5744    0.1917    1.9602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9226   -1.3411    1.1565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7851    1.7169   -1.4298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1109    2.9350    0.6879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9833    1.3928    1.5527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3925    2.3602   -0.8322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7634    2.2534    0.8199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5901   -1.5437    0.6305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9149   -0.9780    1.1510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3849   -0.2585    1.8445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5663    0.7608   -2.1961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7056   -1.6818   -2.5462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2947   -2.0523   -0.8668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3765   -2.3904   -2.4350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6184   -0.7788   -3.1007 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.7148   -2.6863   -1.0998 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2725   -1.8758    1.1890 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1511   -0.2023    0.6006 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8659   -0.7418   -1.1850 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9062   -2.4265   -0.5770 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6751   -0.8140    2.8680 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9356   -2.2914    2.2442 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7343   -2.1533    2.1355 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3767    0.6068   -0.4390 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4237    0.1528    2.4895 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1978    1.7241    1.7232 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1228   -0.0966    3.5534 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5743   -1.1447    3.2589 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0099   -1.6949    2.6455 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6142    0.1149   -0.1606 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1430    1.3221   -2.1912 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3649    2.5839   -3.3769 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0406    2.6133   -2.4872 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
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  3 39  1  0
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  5 42  1  0
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  6 44  1  0
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 27 70  1  0
 28 71  1  0
 29 72  1  0
 30 73  1  0
M  END


  Mrv1652306301800182D          

 36 37  0  0  0  0            999 V2000
    9.2881   11.9625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   10.7250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    9.4875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.8579    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    8.6625    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    6.1875    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    3.7125    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  2  0  0  0  0
 12  9  1  0  0  0  0
 13  9  1  0  0  0  0
 14 10  1  0  0  0  0
 15 10  1  0  0  0  0
 16 11  1  0  0  0  0
 17 11  1  0  0  0  0
 18  7  1  0  0  0  0
 19  8  1  0  0  0  0
 21 20  1  0  0  0  0
 22  1  1  0  0  0  0
 22  2  1  0  0  0  0
 22 12  2  0  0  0  0
 23  3  1  0  0  0  0
 23 13  1  0  0  0  0
 23 14  2  0  0  0  0
 24  4  1  0  0  0  0
 24 15  1  0  0  0  0
 24 16  2  0  0  0  0
 25  5  1  0  0  0  0
 25 17  1  0  0  0  0
 25 20  2  0  0  0  0
 26  6  1  0  0  0  0
 27 21  1  0  0  0  0
 27 26  2  0  0  0  0
 28 18  2  0  0  0  0
 29 19  2  0  0  0  0
 29 28  1  0  0  0  0
 30 26  1  0  0  0  0
 30 28  1  0  0  0  0
 31 27  1  0  0  0  0
 31 29  1  0  0  0  0
 32 30  2  0  0  0  0
 33 31  2  0  0  0  0
 34 14  1  0  0  0  0
 35 16  1  0  0  0  0
 36 20  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0030017

> <DATABASE_NAME>
hmdb

> <SMILES>
[H]\C(CC\C(C)=C(/[H])CC\C(C)=C(/[H])CC1=C(C)C(=O)C2=CC=CC=C2C1=O)=C(\C)CCC=C(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C31H40O2/c1-22(2)12-9-13-23(3)14-10-15-24(4)16-11-17-25(5)20-21-27-26(6)30(32)28-18-7-8-19-29(28)31(27)33/h7-8,12,14,16,18-20H,9-11,13,15,17,21H2,1-6H3/b23-14+,24-16+,25-20+

> <INCHI_KEY>
DKHGMERMDICWDU-GHDNBGIDSA-N

> <FORMULA>
C31H40O2

> <MOLECULAR_WEIGHT>
444.659

> <EXACT_MASS>
444.302830528

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
54.9249299778513

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-methyl-3-[(2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-yl]-1,4-dihydronaphthalene-1,4-dione

> <ALOGPS_LOGP>
7.24

> <JCHEM_LOGP>
8.479707364333333

> <ALOGPS_LOGS>
-5.96

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-7.224343414413889

> <JCHEM_POLAR_SURFACE_AREA>
34.14

> <JCHEM_REFRACTIVITY>
145.50680000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.89e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
menatetrenone

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0030017
     RDKit          3D
Menatetrenone
 73 74  0  0  0  0  0  0  0  0999 V2000
   -9.4523   -0.3062   -1.3208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5857    0.1989   -0.2154 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6441   -0.4797    1.0813 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8004    1.2349   -0.4433 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8925    1.8355    0.5628 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4458    1.7756    0.0925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9856    0.3906   -0.1397 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9530   -0.6532    0.9014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5662    0.0360   -1.3653 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0980   -1.3140   -1.6671 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6651   -1.3548   -2.1361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6861   -0.8442   -1.1679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7203    0.5528   -0.6797 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7198   -1.6692   -0.7170 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3085   -1.2441    0.2586 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6966   -1.3560   -0.2886 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6723   -0.9002    0.7677 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7727   -1.5816    2.0878 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4795    0.1310    0.5472 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4588    0.6428    1.5153 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8483    0.6211    0.9916 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8339   -0.0305    1.5770 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6095   -0.8004    2.8261 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1985   -0.0311    1.0296 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1425   -0.6584    1.5950 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5400    0.6882   -0.1907 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8323    0.6722   -0.6859 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1163    1.3581   -1.8329 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1220    2.0535   -2.4806 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8262    2.0619   -1.9726 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5213    1.3749   -0.8154 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1802    1.3550   -0.2468 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2657    1.9866   -0.8306 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9423   -0.3055   -2.2889 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3153    0.4133   -1.4120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9094   -1.2847   -1.0790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6550   -0.9720    1.1882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5744    0.1917    1.9602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9226   -1.3411    1.1565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7851    1.7169   -1.4298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1109    2.9350    0.6879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9833    1.3928    1.5527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3925    2.3602   -0.8322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7634    2.2534    0.8199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5901   -1.5437    0.6305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9149   -0.9780    1.1510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3849   -0.2585    1.8445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5663    0.7608   -2.1961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7056   -1.6818   -2.5462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2947   -2.0523   -0.8668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3765   -2.3904   -2.4350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6184   -0.7788   -3.1007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6879    0.9959   -0.7799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3968    1.1667   -1.3182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0139    0.6638    0.3636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7148   -2.6863   -1.0998 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2725   -1.8758    1.1890 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1511   -0.2023    0.6006 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8659   -0.7418   -1.1850 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9062   -2.4265   -0.5770 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6751   -0.8140    2.8680 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9356   -2.2914    2.2442 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7343   -2.1533    2.1355 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3767    0.6068   -0.4390 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4237    0.1528    2.4895 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1978    1.7241    1.7232 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1228   -0.0966    3.5534 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5743   -1.1447    3.2589 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0099   -1.6949    2.6455 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6142    0.1149   -0.1606 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1430    1.3221   -2.1912 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3649    2.5839   -3.3769 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0406    2.6133   -2.4872 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  2  0
 24 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  2  0
 31 32  1  0
 32 33  2  0
 32 21  1  0
 31 26  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  3 37  1  0
  3 38  1  0
  3 39  1  0
  4 40  1  0
  5 41  1  0
  5 42  1  0
  6 43  1  0
  6 44  1  0
  8 45  1  0
  8 46  1  0
  8 47  1  0
  9 48  1  0
 10 49  1  0
 10 50  1  0
 11 51  1  0
 11 52  1  0
 13 53  1  0
 13 54  1  0
 13 55  1  0
 14 56  1  0
 15 57  1  0
 15 58  1  0
 16 59  1  0
 16 60  1  0
 18 61  1  0
 18 62  1  0
 18 63  1  0
 19 64  1  0
 20 65  1  0
 20 66  1  0
 23 67  1  0
 23 68  1  0
 23 69  1  0
 27 70  1  0
 28 71  1  0
 29 72  1  0
 30 73  1  0
M  END

HEADER    PROTEIN                                 30-JUN-18   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   30-JUN-18         0                                  
HETATM    1  C   UNK     0      17.338  22.330   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      18.672  20.020   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      16.004  15.400   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.337  10.780   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.669   6.160   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      16.004  18.480   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      13.337  13.860   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.669   9.240   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      16.004  20.020   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      14.670  17.710   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.337  15.400   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.003  13.090   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.669  10.780   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.336   8.470   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.002   6.160   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      17.338  20.790   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      14.670  16.170   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.003  11.550   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.336   6.930   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       5.335   0.000   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       5.335   6.160   0.000  0.00  0.00           O+0
HETATM   34  H   UNK     0      12.003  16.170   0.000  0.00  0.00           H+0
HETATM   35  H   UNK     0       9.336  11.550   0.000  0.00  0.00           H+0
HETATM   36  H   UNK     0       6.668   6.930   0.000  0.00  0.00           H+0
CONECT    1   22                                                            
CONECT    2   22                                                            
CONECT    3   23                                                            
CONECT    4   24                                                            
CONECT    5   25                                                            
CONECT    6   26                                                            
CONECT    7    8   18                                                       
CONECT    8    7   19                                                       
CONECT    9   12   13                                                       
CONECT   10   14   15                                                       
CONECT   11   16   17                                                       
CONECT   12    9   22                                                       
CONECT   13    9   23                                                       
CONECT   14   10   23   34                                                  
CONECT   15   10   24                                                       
CONECT   16   11   24   35                                                  
CONECT   17   11   25                                                       
CONECT   18    7   28                                                       
CONECT   19    8   29                                                       
CONECT   20   21   25   36                                                  
CONECT   21   20   27                                                       
CONECT   22    1    2   12                                                  
CONECT   23    3   13   14                                                  
CONECT   24    4   15   16                                                  
CONECT   25    5   17   20                                                  
CONECT   26    6   27   30                                                  
CONECT   27   21   26   31                                                  
CONECT   28   18   29   30                                                  
CONECT   29   19   28   31                                                  
CONECT   30   26   28   32                                                  
CONECT   31   27   29   33                                                  
CONECT   32   30                                                            
CONECT   33   31                                                            
CONECT   34   14                                                            
CONECT   35   16                                                            
CONECT   36   20                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   74    0
END

COMPND    HMDB0030017
HETATM    1  C1  UNL     1      -9.452  -0.306  -1.321  1.00  0.00           C  
HETATM    2  C2  UNL     1      -8.586   0.199  -0.215  1.00  0.00           C  
HETATM    3  C3  UNL     1      -8.644  -0.480   1.081  1.00  0.00           C  
HETATM    4  C4  UNL     1      -7.800   1.235  -0.443  1.00  0.00           C  
HETATM    5  C5  UNL     1      -6.893   1.835   0.563  1.00  0.00           C  
HETATM    6  C6  UNL     1      -5.446   1.776   0.092  1.00  0.00           C  
HETATM    7  C7  UNL     1      -4.986   0.391  -0.140  1.00  0.00           C  
HETATM    8  C8  UNL     1      -4.953  -0.653   0.901  1.00  0.00           C  
HETATM    9  C9  UNL     1      -4.566   0.036  -1.365  1.00  0.00           C  
HETATM   10  C10 UNL     1      -4.098  -1.314  -1.667  1.00  0.00           C  
HETATM   11  C11 UNL     1      -2.665  -1.355  -2.136  1.00  0.00           C  
HETATM   12  C12 UNL     1      -1.686  -0.844  -1.168  1.00  0.00           C  
HETATM   13  C13 UNL     1      -1.720   0.553  -0.680  1.00  0.00           C  
HETATM   14  C14 UNL     1      -0.720  -1.669  -0.717  1.00  0.00           C  
HETATM   15  C15 UNL     1       0.308  -1.244   0.259  1.00  0.00           C  
HETATM   16  C16 UNL     1       1.697  -1.356  -0.289  1.00  0.00           C  
HETATM   17  C17 UNL     1       2.672  -0.900   0.768  1.00  0.00           C  
HETATM   18  C18 UNL     1       2.773  -1.582   2.088  1.00  0.00           C  
HETATM   19  C19 UNL     1       3.479   0.131   0.547  1.00  0.00           C  
HETATM   20  C20 UNL     1       4.459   0.643   1.515  1.00  0.00           C  
HETATM   21  C21 UNL     1       5.848   0.621   0.992  1.00  0.00           C  
HETATM   22  C22 UNL     1       6.834  -0.030   1.577  1.00  0.00           C  
HETATM   23  C23 UNL     1       6.610  -0.800   2.826  1.00  0.00           C  
HETATM   24  C24 UNL     1       8.199  -0.031   1.030  1.00  0.00           C  
HETATM   25  O1  UNL     1       9.142  -0.658   1.595  1.00  0.00           O  
HETATM   26  C25 UNL     1       8.540   0.688  -0.191  1.00  0.00           C  
HETATM   27  C26 UNL     1       9.832   0.672  -0.686  1.00  0.00           C  
HETATM   28  C27 UNL     1      10.116   1.358  -1.833  1.00  0.00           C  
HETATM   29  C28 UNL     1       9.122   2.053  -2.481  1.00  0.00           C  
HETATM   30  C29 UNL     1       7.826   2.062  -1.973  1.00  0.00           C  
HETATM   31  C30 UNL     1       7.521   1.375  -0.815  1.00  0.00           C  
HETATM   32  C31 UNL     1       6.180   1.355  -0.247  1.00  0.00           C  
HETATM   33  O2  UNL     1       5.266   1.987  -0.831  1.00  0.00           O  
HETATM   34  H1  UNL     1      -8.942  -0.306  -2.289  1.00  0.00           H  
HETATM   35  H2  UNL     1     -10.315   0.413  -1.412  1.00  0.00           H  
HETATM   36  H3  UNL     1      -9.909  -1.285  -1.079  1.00  0.00           H  
HETATM   37  H4  UNL     1      -9.655  -0.972   1.188  1.00  0.00           H  
HETATM   38  H5  UNL     1      -8.574   0.192   1.960  1.00  0.00           H  
HETATM   39  H6  UNL     1      -7.923  -1.341   1.156  1.00  0.00           H  
HETATM   40  H7  UNL     1      -7.785   1.717  -1.430  1.00  0.00           H  
HETATM   41  H8  UNL     1      -7.111   2.935   0.688  1.00  0.00           H  
HETATM   42  H9  UNL     1      -6.983   1.393   1.553  1.00  0.00           H  
HETATM   43  H10 UNL     1      -5.392   2.360  -0.832  1.00  0.00           H  
HETATM   44  H11 UNL     1      -4.763   2.253   0.820  1.00  0.00           H  
HETATM   45  H12 UNL     1      -5.590  -1.544   0.630  1.00  0.00           H  
HETATM   46  H13 UNL     1      -3.915  -0.978   1.151  1.00  0.00           H  
HETATM   47  H14 UNL     1      -5.385  -0.259   1.844  1.00  0.00           H  
HETATM   48  H15 UNL     1      -4.566   0.761  -2.196  1.00  0.00           H  
HETATM   49  H16 UNL     1      -4.706  -1.682  -2.546  1.00  0.00           H  
HETATM   50  H17 UNL     1      -4.295  -2.052  -0.867  1.00  0.00           H  
HETATM   51  H18 UNL     1      -2.376  -2.390  -2.435  1.00  0.00           H  
HETATM   52  H19 UNL     1      -2.618  -0.779  -3.101  1.00  0.00           H  
HETATM   53  H20 UNL     1      -0.688   0.996  -0.780  1.00  0.00           H  
HETATM   54  H21 UNL     1      -2.397   1.167  -1.318  1.00  0.00           H  
HETATM   55  H22 UNL     1      -2.014   0.664   0.364  1.00  0.00           H  
HETATM   56  H23 UNL     1      -0.715  -2.686  -1.100  1.00  0.00           H  
HETATM   57  H24 UNL     1       0.273  -1.876   1.189  1.00  0.00           H  
HETATM   58  H25 UNL     1       0.151  -0.202   0.601  1.00  0.00           H  
HETATM   59  H26 UNL     1       1.866  -0.742  -1.185  1.00  0.00           H  
HETATM   60  H27 UNL     1       1.906  -2.426  -0.577  1.00  0.00           H  
HETATM   61  H28 UNL     1       2.675  -0.814   2.868  1.00  0.00           H  
HETATM   62  H29 UNL     1       1.936  -2.291   2.244  1.00  0.00           H  
HETATM   63  H30 UNL     1       3.734  -2.153   2.136  1.00  0.00           H  
HETATM   64  H31 UNL     1       3.377   0.607  -0.439  1.00  0.00           H  
HETATM   65  H32 UNL     1       4.424   0.153   2.489  1.00  0.00           H  
HETATM   66  H33 UNL     1       4.198   1.724   1.723  1.00  0.00           H  
HETATM   67  H34 UNL     1       6.123  -0.097   3.553  1.00  0.00           H  
HETATM   68  H35 UNL     1       7.574  -1.145   3.259  1.00  0.00           H  
HETATM   69  H36 UNL     1       6.010  -1.695   2.646  1.00  0.00           H  
HETATM   70  H37 UNL     1      10.614   0.115  -0.161  1.00  0.00           H  
HETATM   71  H38 UNL     1      11.143   1.322  -2.191  1.00  0.00           H  
HETATM   72  H39 UNL     1       9.365   2.584  -3.377  1.00  0.00           H  
HETATM   73  H40 UNL     1       7.041   2.613  -2.487  1.00  0.00           H  
CONECT    1    2   34   35   36
CONECT    2    3    4    4
CONECT    3   37   38   39
CONECT    4    5   40
CONECT    5    6   41   42
CONECT    6    7   43   44
CONECT    7    8    9    9
CONECT    8   45   46   47
CONECT    9   10   48
CONECT   10   11   49   50
CONECT   11   12   51   52
CONECT   12   13   14   14
CONECT   13   53   54   55
CONECT   14   15   56
CONECT   15   16   57   58
CONECT   16   17   59   60
CONECT   17   18   19   19
CONECT   18   61   62   63
CONECT   19   20   64
CONECT   20   21   65   66
CONECT   21   22   22   32
CONECT   22   23   24
CONECT   23   67   68   69
CONECT   24   25   25   26
CONECT   26   27   27   31
CONECT   27   28   70
CONECT   28   29   29   71
CONECT   29   30   72
CONECT   30   31   31   73
CONECT   31   32
CONECT   32   33   33
END

HMDB0030017
     RDKit          3D
Menatetrenone
 73 74  0  0  0  0  0  0  0  0999 V2000
   -9.4523   -0.3062   -1.3208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5857    0.1989   -0.2154 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6441   -0.4797    1.0813 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8004    1.2349   -0.4433 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8925    1.8355    0.5628 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4458    1.7756    0.0925 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9856    0.3906   -0.1397 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9530   -0.6532    0.9014 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5662    0.0360   -1.3653 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0980   -1.3140   -1.6671 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6651   -1.3548   -2.1361 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6861   -0.8442   -1.1679 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7203    0.5528   -0.6797 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7198   -1.6692   -0.7170 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3085   -1.2441    0.2586 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6966   -1.3560   -0.2886 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6723   -0.9002    0.7677 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7727   -1.5816    2.0878 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4795    0.1310    0.5472 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4588    0.6428    1.5153 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8483    0.6211    0.9916 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8339   -0.0305    1.5770 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6095   -0.8004    2.8261 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1985   -0.0311    1.0296 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1425   -0.6584    1.5950 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5400    0.6882   -0.1907 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8323    0.6722   -0.6859 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1163    1.3581   -1.8329 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1220    2.0535   -2.4806 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8262    2.0619   -1.9726 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5213    1.3749   -0.8154 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1802    1.3550   -0.2468 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2657    1.9866   -0.8306 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9423   -0.3055   -2.2889 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3153    0.4133   -1.4120 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9094   -1.2847   -1.0790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6550   -0.9720    1.1882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5744    0.1917    1.9602 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9226   -1.3411    1.1565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7851    1.7169   -1.4298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1109    2.9350    0.6879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9833    1.3928    1.5527 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3925    2.3602   -0.8322 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7634    2.2534    0.8199 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5901   -1.5437    0.6305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9149   -0.9780    1.1510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3849   -0.2585    1.8445 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5663    0.7608   -2.1961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7056   -1.6818   -2.5462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2947   -2.0523   -0.8668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3765   -2.3904   -2.4350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6184   -0.7788   -3.1007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6879    0.9959   -0.7799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3968    1.1667   -1.3182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0139    0.6638    0.3636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7148   -2.6863   -1.0998 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2725   -1.8758    1.1890 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1511   -0.2023    0.6006 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8659   -0.7418   -1.1850 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9062   -2.4265   -0.5770 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6751   -0.8140    2.8680 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9356   -2.2914    2.2442 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7343   -2.1533    2.1355 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3767    0.6068   -0.4390 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4237    0.1528    2.4895 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1978    1.7241    1.7232 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1228   -0.0966    3.5534 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5743   -1.1447    3.2589 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0099   -1.6949    2.6455 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.6142    0.1149   -0.1606 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1430    1.3221   -2.1912 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3649    2.5839   -3.3769 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0406    2.6133   -2.4872 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  2  0
 19 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 22 24  1  0
 24 25  2  0
 24 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  2  0
 31 32  1  0
 32 33  2  0
 32 21  1  0
 31 26  1  0
  1 34  1  0
  1 35  1  0
  1 36  1  0
  3 37  1  0
  3 38  1  0
  3 39  1  0
  4 40  1  0
  5 41  1  0
  5 42  1  0
  6 43  1  0
  6 44  1  0
  8 45  1  0
  8 46  1  0
  8 47  1  0
  9 48  1  0
 10 49  1  0
 10 50  1  0
 11 51  1  0
 11 52  1  0
 13 53  1  0
 13 54  1  0
 13 55  1  0
 14 56  1  0
 15 57  1  0
 15 58  1  0
 16 59  1  0
 16 60  1  0
 18 61  1  0
 18 62  1  0
 18 63  1  0
 19 64  1  0
 20 65  1  0
 20 66  1  0
 23 67  1  0
 23 68  1  0
 23 69  1  0
 27 70  1  0
 28 71  1  0
 29 72  1  0
 30 73  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
2-Methyl-3-(3,7,11,15-tetramethyl-2,6,10,14-hexadecatetraenyl)-1,4-naphthoquinone	ChEBI
2-Methyl-3-geranylgeranyl-1,4-naphthoquinone	ChEBI
2-Methyl-3-trans-tetraprenyl-1,4-naphthoquinone	ChEBI
Menaquinone 4	ChEBI
Menaquinone K4	ChEBI
Menatetrenona	ChEBI
Menatetrenonum	ChEBI
MK-4	ChEBI
MK4	ChEBI
Vitamin K2(20)	ChEBI
Vitamin MK 4	ChEBI
Vitamin K2	Kegg
Menaquinone-4	ChEBI
(e,e,e)-Isomer OF menatetrenone	MeSH, HMDB
2-Methyl-3-all-trans-tetraprenyl-1,4-naphthoquinone	MeSH, HMDB
Kefton-2	MeSH, HMDB
Vitamin MK-4	MeSH, HMDB
Vitamin K 2	MeSH
Vitamin K quinone	MeSH
Menaquinone	MeSH
Menaquinones	MeSH

Chemical Formula

C₃₁H₄₀O₂

Average Molecular Weight

444.659

Monoisotopic Molecular Weight

444.302830528

IUPAC Name

2-methyl-3-[(2E,6E,10E)-3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraen-1-yl]-1,4-dihydronaphthalene-1,4-dione

Traditional Name

menatetrenone

CAS Registry Number

863-61-6

SMILES

CC(C)=CCC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC1=C(C)C(=O)C2=CC=CC=C2C1=O

InChI Identifier

InChI=1S/C31H40O2/c1-22(2)12-9-13-23(3)14-10-15-24(4)16-11-17-25(5)20-21-27-26(6)30(32)28-18-7-8-19-29(28)31(27)33/h7-8,12,14,16,18-20H,9-11,13,15,17,21H2,1-6H3/b23-14+,24-16+,25-20+

InChI Key

DKHGMERMDICWDU-GHDNBGIDSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as menaquinones. These are vitamin K2 compounds consisting of a naphtho-1,4-quinone ring system, which is substituted at the 2-position by an isoprenyl side-chain, and usually, at the 3-position by a methyl group.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Quinone and hydroquinone lipids

Direct Parent

Menaquinones

Alternative Parents

Substituents

Menaquinone
Diterpenoid
Naphthoquinone
Naphthalene
Aryl ketone
Quinone
Benzenoid
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic compounds

External Descriptors

menaquinone (CHEBI:78277 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cytoplasm (HMDB: HMDB0030017)
Cell membrane (HMDB: HMDB0030017)

Cellular substructure

Organelle

Mitochondria

Mitochondria (HMDB: HMDB0030017)

Extracellular (HMDB: HMDB0030017)
Membrane (HMDB: HMDB0030017)

Biofluid or Excreta

Excreta

Urine (PMID: 32966057)

Non-excretory biofluid

Blood (PMID: 32966057)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0030017)

Source

Endogenous

Endogenous (HMDB: HMDB0030017)

Plant

Plant (HMDB: HMDB0030017)

Animal

Animal (HMDB: HMDB0030017)

Exogenous

Food

Food (HMDB: HMDB0030017)

Animal origin

Poultry

Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Anatidae (FooDB: FOOD00576)
Quail (FooDB: FOOD00541)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Emu (FooDB: FOOD00360)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Velvet duck (FooDB: FOOD00427)
Ostrich (FooDB: FOOD00422)

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Lagomorph

Bovine

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Equine

Horse (FooDB: FOOD00378)

Nut

Almond (FooDB: FOOD00148)

Vegetable

Cabbage

Cauliflower (FooDB: FOOD00031)
Kale (FooDB: FOOD00390)

Fruit vegetable

Root vegetable

Prairie turnip (FooDB: FOOD00439)

Mushroom

Other vegetable

Narrowleaf cattail (FooDB: FOOD00564)

Tuber

Potato (FooDB: FOOD00175)

Leaf vegetable

Lambsquarters (FooDB: FOOD00394)

Vegetable product

Other vegetable product (FooDB: FOOD00671)

Cereal and cereal product

Cereal

Cereal product

Flat bread

Tortilla (FooDB: FOOD00709)
Piki bread (FooDB: FOOD00806)

Leavened bread

Pan dulce (FooDB: FOOD00816)

Herb and spice

Herb

Amaranth (FooDB: FOOD00288)
Rose hip (FooDB: FOOD00446)
Teff (FooDB: FOOD00489)

Spice

Wasabi (FooDB: FOOD00498)

Other seed

Quinoa (FooDB: FOOD00441)

Pacific cod (FooDB: FOOD00337)
Hippoglossus (Common halibut) (FooDB: FOOD00375)
Sheefish (FooDB: FOOD00472)
Pacific rockfish (FooDB: FOOD00426)
Sockeye salmon (FooDB: FOOD00453)
Pollock (FooDB: FOOD00513)
Atlantic halibut (FooDB: FOOD00516)
Pacific halibut (FooDB: FOOD00517)
Lemon sole (FooDB: FOOD00583)
Gadiformes (FooDB: FOOD00580)
Flatfish (FooDB: FOOD00535)
Pacific ocean perch (FooDB: FOOD00598)
True sole (FooDB: FOOD00604)
Rainbow trout (FooDB: FOOD00444)
Catfish (FooDB: FOOD00605)
Whitefish (FooDB: FOOD00503)
Channel catfish (FooDB: FOOD00324)
Painted comber (FooDB: FOOD00294)
Alaska pollock (FooDB: FOOD00497)
Chum salmon (FooDB: FOOD00451)
Atlantic salmon (FooDB: FOOD00455)
Chinook salmon (FooDB: FOOD00454)
Pink salmon (FooDB: FOOD00450)
Smelt (FooDB: FOOD00519)

Mollusk

Eastern oyster (FooDB: FOOD00356)
Scallop (FooDB: FOOD00462)
Bivalvia (Clam, Mussel, Oyster) (FooDB: FOOD00531)

Bivalvia

Clam (FooDB: FOOD00952)

Fish product

Other fish product (FooDB: FOOD00665)

Pinniped

Bearded seal (FooDB: FOOD00466)
Spotted seal (FooDB: FOOD00423)

Cetacean

Beluga whale (FooDB: FOOD00300)

Fruit

Tropical fruit

Pome

Apple (FooDB: FOOD00105)
Pear (FooDB: FOOD00152)

Berry

Rubus (Blackberry, Raspberry) (FooDB: FOOD00160)
Vaccinium (Blueberry, Cranberry, Huckleberry) (FooDB: FOOD00188)
Salmonberry (FooDB: FOOD00456)
Alaska blueberry (FooDB: FOOD00380)

Drupe

Milk and milk product

Fermented milk product

Other milk product

Almond milk (FooDB: FOOD00937)

Unfermented milk

Milk (Cow) (FooDB: FOOD00618)
Cow milk, pasteurized, vitamin D added, 3.25% fat (FooDB: FOOD00892)

Baby food

Baby food (FooDB: FOOD00668)

Pulse

Bean

Common bean (FooDB: FOOD00134)
Green bean (FooDB: FOOD00883)

Pea

Common pea (FooDB: FOOD00141)

Baking good

Leavening agent (FooDB: FOOD00661)
Cooking oil (FooDB: FOOD00779)

Dressing

Salad dressing (FooDB: FOOD00645)

Wrapper

Pie crust (FooDB: FOOD00780)

Soy

Soy bean (FooDB: FOOD00085)

Soy product

Other soy product (FooDB: FOOD00271)

Unclassified food or beverage

Unclassified food or beverage (FooDB: FOOD00672)

Dish

Ground meat

Other dish

Other dish (FooDB: FOOD00836)
Pizza (FooDB: FOOD00637)
Soup (FooDB: FOOD00670)
Salad (FooDB: FOOD00712)
Pot pie (FooDB: FOOD00837)
Frybread (FooDB: FOOD00728)
Stew (FooDB: FOOD00724)

Pasta dish

Macaroni and cheese (FooDB: FOOD00759)
Ravioli (FooDB: FOOD00791)

Sandwich

Other sandwich (FooDB: FOOD00755)

Asian cuisine

Egg roll (FooDB: FOOD00717)

Latin american cuisine

Tamale (FooDB: FOOD00795)
Arepa (FooDB: FOOD00831)
Empanada (FooDB: FOOD00830)
Pupusa (FooDB: FOOD00829)

Cocoa and cocoa product

Cocoa product

Chocolate (FooDB: FOOD00687)

Fat and oil

Vegetable fat

Margarine-like spread (FooDB: FOOD00844)
Margarine (FooDB: FOOD00843)

Snack

Confectionery

Dessert

Pastry (FooDB: FOOD00641)
Pie (FooDB: FOOD00782)
Pudding (FooDB: FOOD00734)

Candy

Other candy (FooDB: FOOD00679)

Spread

Dulce de leche (FooDB: FOOD00714)

Milk dessert

Sweet custard (FooDB: FOOD00716)

Gourd

Cucumber (FooDB: FOOD00065)
Cucurbita (FooDB: FOOD00066)
Japanese pumpkin (FooDB: FOOD00886)
Sunburst squash (pattypan squash) (FooDB: FOOD00874)

Egg

Eggs (FooDB: FOOD00619)

Beverage

Other beverage

Horchata (FooDB: FOOD00823)
Fruit-flavor drink (FooDB: FOOD00821)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid peroxidation (HMDB: HMDB0030017)

Biochemical process

Fatty acid metabolism (HMDB: HMDB0030017)

Cellular process

Cell signaling (HMDB: HMDB0030017)

Biochemical pathway

Lipid metabolism pathway (HMDB: HMDB0030017)

Role

Biological role

Membrane stabilizer (HMDB: HMDB0030017)

Nutrient

Nutrient (HMDB: HMDB0030017)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0030017)

Emulsifier (HMDB: HMDB0030017)

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Experimental Collision Cross Sections

Adduct Type	Data Source	CCS Value (Å²)	Reference
[M+H]+	Not Available	198.662	http://allccs.zhulab.cn/database/detail?ID=AllCCS00001978

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.00027 g/L	ALOGPS
logP	7.24	ALOGPS
logP	8.48	ChemAxon
logS	-6	ALOGPS
pKa (Strongest Basic)	-7.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	34.14 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	145.51 m³·mol⁻¹	ChemAxon
Polarizability	54.92 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	212.253	30932474
DeepCCS	[M-H]-	209.895	30932474
DeepCCS	[M-2H]-	243.191	30932474
DeepCCS	[M+Na]+	218.991	30932474
AllCCS	[M+H]+	220.8	32859911
AllCCS	[M+H-H2O]+	218.6	32859911
AllCCS	[M+NH4]+	222.8	32859911
AllCCS	[M+Na]+	223.4	32859911
AllCCS	[M-H]-	203.8	32859911
AllCCS	[M+Na-2H]-	205.2	32859911
AllCCS	[M+HCOO]-	207.0	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Menatetrenone	CC(C)=CCC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC1=C(C)C(=O)C2=CC=CC=C2C1=O	4335.1	Standard polar	33892256
Menatetrenone	CC(C)=CCC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC1=C(C)C(=O)C2=CC=CC=C2C1=O	3406.0	Standard non polar	33892256
Menatetrenone	CC(C)=CCC\C(C)=C\CC\C(C)=C\CC\C(C)=C\CC1=C(C)C(=O)C2=CC=CC=C2C1=O	3458.5	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Experimental GC-MS	GC-MS Spectrum - Menatetrenone EI-B (Non-derivatized)	splash10-014l-9430000000-936e4020e35c79ab80a8	2017-09-12	HMDB team, MONA, MassBank	View Spectrum
Experimental GC-MS	GC-MS Spectrum - Menatetrenone EI-B (Non-derivatized)	splash10-014l-9430000000-936e4020e35c79ab80a8	2018-05-18	HMDB team, MONA, MassBank	View Spectrum
Experimental GC-MS	GC-MS Spectrum - Menatetrenone EI-B (Non-derivatized)	splash10-003r-7891050000-fb45abd0445fd13b3287	2018-05-25	HMDB team, MONA, MassBank	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Menatetrenone GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Menatetrenone 10V, Positive-QTOF	splash10-0002-0221900000-da2fa06091b3f02f7f62	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Menatetrenone 20V, Positive-QTOF	splash10-0550-0968100000-d9351f8233d2638c6648	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Menatetrenone 40V, Positive-QTOF	splash10-014i-9673000000-f5a80c46af487a0ae786	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Menatetrenone 10V, Negative-QTOF	splash10-0006-0000900000-a5b1daed1e13ae9cdc49	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Menatetrenone 20V, Negative-QTOF	splash10-0006-0101900000-63826c82750026b58641	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Menatetrenone 40V, Negative-QTOF	splash10-00fr-2925400000-e48e5e86379a4048f95e	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Menatetrenone 10V, Positive-QTOF	splash10-0002-2137900000-9bfb9ad4ac1145915e57	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Menatetrenone 20V, Positive-QTOF	splash10-0019-3419100000-17e116bda37eb38893dc	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Menatetrenone 40V, Positive-QTOF	splash10-007a-3901000000-9c3d341cbd4ad0feec93	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Menatetrenone 10V, Negative-QTOF	splash10-0006-0000900000-87177730a5d4e2d424bb	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Menatetrenone 20V, Negative-QTOF	splash10-000f-0902700000-70d2be403d22d9bb2275	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Menatetrenone 40V, Negative-QTOF	splash10-002s-2923100000-7822153ffca689168909	2021-09-22	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	2022-08-20	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

Blood
Urine

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Normal	32966057	details
Urine	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Normal	32966057	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

DB12148

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB029792

KNApSAcK ID

Not Available

Chemspider ID

4445530

KEGG Compound ID

C00828

BioCyc ID

CPD-9726

BiGG ID

Not Available

Wikipedia Link

Menatetrenone

METLIN ID

Not Available

PubChem Compound

5282367

PDB ID

Not Available

ChEBI ID

78277

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Enzymes

Enzyme Details

1. NAD(P)H dehydrogenase [quinone] 1

General function:: Involved in electron carrier activity
Specific function:: The enzyme apparently serves as a quinone reductase in connection with conjugation reactions of hydroquinons involved in detoxification pathways as well as in biosynthetic processes such as the vitamin K-dependent gamma-carboxylation of glutamate residues in prothrombin synthesis.
Gene Name:: NQO1
Uniprot ID:: P15559
Molecular weight:: 30867.405

Reactions

Menatetrenone + Hydrogen Ion + NADH → Menaquinol + NAD	details

Enzyme Details

2. Vitamin K epoxide reductase complex subunit 1

General function:: Involved in vitamin-K-epoxide reductase (warfarin-sensi
Specific function:: Involved in vitamin K metabolism. Catalytic subunit of the vitamin K epoxide reductase (VKOR) complex which reduces inactive vitamin K 2,3-epoxide to active vitamin K.
Gene Name:: VKORC1
Uniprot ID:: Q9BQB6
Molecular weight:: 18234.3

Reactions

2,3-Epoxymenaquinone + 1,4-Dithiothreitol → Menatetrenone + Oxidized dithiothreitol + Water	details

Showing metabocard for Menatetrenone (HMDB0030017)

MOL for HMDB0030017 (Menatetrenone)

3D MOL for HMDB0030017 (Menatetrenone)

3D SDF for HMDB0030017 (Menatetrenone)

3D-SDF for HMDB0030017 (Menatetrenone)

PDB for HMDB0030017 (Menatetrenone)

3D PDB for HMDB0030017 (Menatetrenone)

SMILES for HMDB0030017 (Menatetrenone)

INCHI for HMDB0030017 (Menatetrenone)

Structure for HMDB0030017 (Menatetrenone)

3D Structure for HMDB0030017 (Menatetrenone)

Experimental Collision Cross Sections

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

Enzymes

Reactions

Reactions