Hmdb loader

Showing metabocard for PC(14:0/14:0) (HMDB0007866)

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IdentificationTaxonomyOntologyPhysical propertiesSpectraBiological propertiesConcentrationsLinksReferencesenzymes (77)transporters (1) Show 78 proteinsXML
enzymes (77)transporters (1) Show 78 proteins
Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2008-09-12 01:27:25 UTC
Update Date2022-11-30 19:03:05 UTC
HMDB IDHMDB0007866
Secondary Accession Numbers
  • HMDB07866
Metabolite Identification
Common NamePC(14:0/14:0)
DescriptionPC(14:0/14:0) is a phosphatidylcholine (PC or GPCho). It is a glycerophospholipid in which a phosphorylcholine moiety occupies a glycerol substitution site. As is the case with diacylglycerols, glycerophosphocholines can have many different combinations of fatty acids of varying lengths and saturation attached at the C-1 and C-2 positions. Fatty acids containing 16, 18 and 20 carbons are the most common. PC(14:0/14:0), in particular, consists of two chains of myristic acid at the C-1 and C-2 positions. The myristic acid moieties are derived from nutmeg and butter. Phospholipids, are ubiquitous in nature and are key components of the lipid bilayer of cells, as well as being involved in metabolism and signaling.While most phospholipids have a saturated fatty acid on C-1 and an unsaturated fatty acid on C-2 of the glycerol backbone, the fatty acid distribution at the C-1 and C-2 positions of glycerol within phospholipids is continually in flux, owing to phospholipid degradation and the continuous phospholipid remodeling that occurs while these molecules are in membranes. PCs can be synthesized via three different routes. In one route, choline is activated first by phosphorylation and then by coupling to CDP prior to attachment to phosphatidic acid. PCs can also synthesized by the addition of choline to CDP-activated 1,2-diacylglycerol. A third route to PC synthesis involves the conversion of either PS or PE to PC.
Structure
Data?1582752508
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0007866 (PC(14:0/14:0))

PC(14:0/14:0)
  Mrv1652303192020102D          

 47 46  0  0  0  0            999 V2000
   -3.8021    0.3608    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9591    0.3596    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2447    0.7720    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6571    1.4866    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1679    0.0575    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -3.0969    0.7716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3824    0.3590    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6679    0.7716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9699   -0.3555    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7950   -0.3555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4699    1.1846    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1844    0.7721    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8988    1.1846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6132    0.7721    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    2.2007    0.0576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2744    1.6358    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3277    0.3596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5121    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5121    1.5410    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2263    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9404    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6545    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3686    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0827    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.5095   -0.7680    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  3  2  1  0  0  0  0
  4  3  2  0  0  0  0
  5  3  1  0  0  0  0
  7  6  1  0  0  0  0
  8  7  1  0  0  0  0
  7  9  1  1  0  0  0
  6  1  1  0  0  0  0
  2  8  1  0  0  0  0
  7 10  1  6  0  0  0
  1 18  1  0  0  0  0
 10 33  1  0  0  0  0
 11 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
 14 16  1  0  0  0  0
 14 17  1  0  0  0  0
 11  3  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
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 28 29  1  0  0  0  0
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 31 32  1  0  0  0  0
 33 34  2  0  0  0  0
 33 35  1  0  0  0  0
 35 36  1  0  0  0  0
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 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
M  CHG  2   5  -1  14   1
M  END
Download

3D MOL for HMDB0007866 (PC(14:0/14:0))

HMDB0007866
     RDKit          3D
PC(14:0/14:0)
118117  0  0  0  0  0  0  0  0999 V2000
   -1.2513    1.3811    4.0414 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2355    1.3051    4.1982 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9569    2.5834    3.9364 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7627    3.1312    2.5390 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5394    4.4218    2.4137 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4323    5.0805    1.0861 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9482    4.1997   -0.0269 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8474    4.8807   -1.3622 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3441    4.0958   -2.5144 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6578    2.7907   -2.7770 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1972    2.9253   -3.0314 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4321    1.6012   -3.3057 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1333    0.9257   -4.5247 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5600   -0.3800   -4.7507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3373   -0.9978   -5.8233 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.3145    0.9999   -2.2471 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.2892    1.9894   -0.0541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8847    1.9883    0.1530 N   0  0  0  0  0  4  0  0  0  0  0  0
   -3.6298    2.8791    1.2971 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1793    2.6237   -0.9669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2684    0.7337    0.4203 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0976   -2.7280   -1.7893 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0267   -3.9245   -1.0973 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7335   -4.8698   -1.5315 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.4562   -5.6519    1.9152 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.8541   -5.7548    2.8549 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6861   -4.8216    3.9543 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9691   -3.3895    3.8920 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3509   -2.9107    3.6623 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0492   -3.1927    2.3992 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3898   -2.5446    1.1918 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1059   -2.8726   -0.0819 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1686   -4.3445   -0.3968 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9229   -4.5361   -1.7072 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.4964    5.8031   -1.2844 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8191    5.2962   -1.5300 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4241    4.6988   -3.4570 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4188    3.8285   -2.2892 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1147    2.3982   -3.7248 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8964    2.0611   -2.0005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0001    3.5883   -3.9261 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.5969   -1.9505   -1.8099 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.5738    2.9872   -0.4546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3691    3.7021    1.2876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7782    2.2507    2.2200 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.8708   -6.0250    2.5288 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4721   -6.7724    3.2591 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6475   -5.0078    4.4154 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.2660   -4.2439    2.2490 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  CHG  2  23  -1  27   1
M  END
Download

3D SDF for HMDB0007866 (PC(14:0/14:0))

PC(14:0/14:0)
  Mrv1652303192020102D          

 47 46  0  0  0  0            999 V2000
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M  CHG  2   5  -1  14   1
M  END
> <DATABASE_ID>
HMDB0007866

> <DATABASE_NAME>
hmdb

> <SMILES>
[H][C@@](COC(=O)CCCCCCCCCCCCC)(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C36H72NO8P/c1-6-8-10-12-14-16-18-20-22-24-26-28-35(38)42-32-34(33-44-46(40,41)43-31-30-37(3,4)5)45-36(39)29-27-25-23-21-19-17-15-13-11-9-7-2/h34H,6-33H2,1-5H3/t34-/m1/s1

> <INCHI_KEY>
CITHEXJVPOWHKC-UUWRZZSWSA-N

> <FORMULA>
C36H72NO8P

> <MOLECULAR_WEIGHT>
677.9325

> <EXACT_MASS>
677.499554797

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
118

> <JCHEM_AVERAGE_POLARIZABILITY>
82.60128947469977

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2-{[(2R)-2,3-bis(tetradecanoyloxy)propyl phosphono]oxy}ethyl)trimethylazanium

> <ALOGPS_LOGP>
4.57

> <JCHEM_LOGP>
6.3355217191949205

> <ALOGPS_LOGS>
-7.26

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8550572064469137

> <JCHEM_PKA_STRONGEST_BASIC>
-6.744159309169687

> <JCHEM_POLAR_SURFACE_AREA>
111.19000000000003

> <JCHEM_REFRACTIVITY>
197.4611

> <JCHEM_ROTATABLE_BOND_COUNT>
36

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.03e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2-{[(2R)-2,3-bis(tetradecanoyloxy)propyl phosphono]oxy}ethyl)trimethylazanium

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0007866 (PC(14:0/14:0))

HMDB0007866
     RDKit          3D
PC(14:0/14:0)
118117  0  0  0  0  0  0  0  0999 V2000
   -1.2513    1.3811    4.0414 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.2897    0.9426   -2.4010 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2318    0.7503   -4.3755 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0049    1.6096   -5.3763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7138   -2.0658   -5.0118 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3005   -2.9651   -4.2979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4025   -3.5682   -3.1157 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5554   -0.5821   -2.3975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5969   -1.9505   -1.8099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9381    1.2000   -1.0873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8533   -0.0638   -0.5222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8384    1.9089    0.9224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5738    2.9872   -0.4546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3691    3.7021    1.2876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7782    2.2507    2.2200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5925    3.2228    1.3141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6763    3.6051   -1.1871 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2161    1.9193   -1.8170 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1195    2.7456   -0.6745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9647   -0.1069    0.1936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0662    0.6506    1.5085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2887    0.5984   -0.0867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4678   -3.3482    0.8649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1046   -3.9243   -0.1205 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4280   -5.5963    0.9908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1433   -6.2571   -0.0392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7270   -6.6354    2.3720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6849   -4.9079    2.7197 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3153   -4.7670    0.9486 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2270   -6.5145    1.0110 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8708   -6.0250    2.5288 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4721   -6.7724    3.2591 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6475   -5.0078    4.4154 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3435   -5.2249    4.8154 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6769   -2.9679    4.9184 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2722   -2.8149    3.2181 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9766   -3.1417    4.5720 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2803   -1.7606    3.7205 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2660   -4.2439    2.2490 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0671   -2.6694    2.4832 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3293   -2.7658    1.1536 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5475   -1.4383    1.3543 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5475   -2.3885   -0.9160 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1457   -2.4494   -0.0355 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1500   -4.7625   -0.5516 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6694   -4.9467    0.3817 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0979   -3.5513   -2.1991 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3717   -5.2203   -2.3666 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9263   -4.9741   -1.4848 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
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 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  2  0
 21 23  1  0
 21 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 27 29  1  0
 27 30  1  0
 18 31  1  0
 31 32  1  0
 32 33  2  0
 32 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  1  0
 39 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  1  0
 43 44  1  0
 44 45  1  0
 45 46  1  0
  1 47  1  0
  1 48  1  0
  1 49  1  0
  2 50  1  0
  2 51  1  0
  3 52  1  0
  3 53  1  0
  4 54  1  0
  4 55  1  0
  5 56  1  0
  5 57  1  0
  6 58  1  0
  6 59  1  0
  7 60  1  0
  7 61  1  0
  8 62  1  0
  8 63  1  0
  9 64  1  0
  9 65  1  0
 10 66  1  0
 10 67  1  0
 11 68  1  0
 11 69  1  0
 12 70  1  0
 12 71  1  0
 13 72  1  0
 13 73  1  0
 17 74  1  0
 17 75  1  0
 18 76  1  6
 19 77  1  0
 19 78  1  0
 25 79  1  0
 25 80  1  0
 26 81  1  0
 26 82  1  0
 28 83  1  0
 28 84  1  0
 28 85  1  0
 29 86  1  0
 29 87  1  0
 29 88  1  0
 30 89  1  0
 30 90  1  0
 30 91  1  0
 34 92  1  0
 34 93  1  0
 35 94  1  0
 35 95  1  0
 36 96  1  0
 36 97  1  0
 37 98  1  0
 37 99  1  0
 38100  1  0
 38101  1  0
 39102  1  0
 39103  1  0
 40104  1  0
 40105  1  0
 41106  1  0
 41107  1  0
 42108  1  0
 42109  1  0
 43110  1  0
 43111  1  0
 44112  1  0
 44113  1  0
 45114  1  0
 45115  1  0
 46116  1  0
 46117  1  0
 46118  1  0
M  CHG  2  23  -1  27   1
M  END
Download

PDB for HMDB0007866 (PC(14:0/14:0))

HEADER    PROTEIN                                 19-MAR-20   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: PC(14:0/14:0)                                     
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-MAR-20         0                                  
HETATM    1  O   UNK     0      -7.097   0.673   0.000  0.00  0.00           O+0
HETATM    2  O   UNK     0      -1.790   0.671   0.000  0.00  0.00           O+0
HETATM    3  P   UNK     0      -0.457   1.441   0.000  0.00  0.00           P+0
HETATM    4  O   UNK     0      -1.227   2.775   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       0.313   0.107   0.000  0.00  0.00           O-1
HETATM    6  C   UNK     0      -5.781   1.440   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.447   0.670   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.113   1.440   0.000  0.00  0.00           C+0
HETATM    9  H   UNK     0      -3.677  -0.664   0.000  0.00  0.00           H+0
HETATM   10  O   UNK     0      -5.217  -0.664   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       0.877   2.211   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.211   1.441   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.544   2.211   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0       4.878   1.441   0.000  0.00  0.00           N+1
HETATM   15  C   UNK     0       4.108   0.108   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.112   3.054   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.212   0.671   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -8.423   1.436   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -8.423   2.876   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -9.756   0.665   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0     -11.089   1.436   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0     -12.422   0.665   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0     -13.755   1.436   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0     -15.088   0.665   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0     -16.421   1.436   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0     -17.754   0.665   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0     -19.087   1.436   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0     -20.420   0.665   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0     -21.753   1.436   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0     -23.086   0.665   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0     -24.419   1.436   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0     -25.752   0.665   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -6.551  -1.434   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -6.551  -2.874   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -7.884  -0.662   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -9.217  -1.434   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0     -10.550  -0.662   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0     -11.883  -1.434   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0     -13.216  -0.662   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0     -14.549  -1.434   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0     -15.882  -0.662   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0     -17.215  -1.434   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0     -18.548  -0.662   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0     -19.881  -1.434   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0     -21.214  -0.662   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0     -22.547  -1.434   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0     -23.880  -0.662   0.000  0.00  0.00           C+0
CONECT    1    6   18                                                       
CONECT    2    3    8                                                       
CONECT    3    2    4    5   11                                             
CONECT    4    3                                                            
CONECT    5    3                                                            
CONECT    6    7    1                                                       
CONECT    7    6    8    9   10                                             
CONECT    8    7    2                                                       
CONECT    9    7                                                            
CONECT   10    7   33                                                       
CONECT   11   12    3                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16   17                                             
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   14                                                            
CONECT   18    1   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31                                                            
CONECT   33   10   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46                                                            
MASTER        0    0    0    0    0    0    0    0   47    0   92    0
END
Download

3D PDB for HMDB0007866 (PC(14:0/14:0))

COMPND    HMDB0007866
HETATM    1  C1  UNL     1      -1.251   1.381   4.041  1.00  0.00           C  
HETATM    2  C2  UNL     1       0.235   1.305   4.198  1.00  0.00           C  
HETATM    3  C3  UNL     1       0.957   2.583   3.936  1.00  0.00           C  
HETATM    4  C4  UNL     1       0.763   3.131   2.539  1.00  0.00           C  
HETATM    5  C5  UNL     1       1.539   4.422   2.414  1.00  0.00           C  
HETATM    6  C6  UNL     1       1.432   5.080   1.086  1.00  0.00           C  
HETATM    7  C7  UNL     1       1.948   4.200  -0.027  1.00  0.00           C  
HETATM    8  C8  UNL     1       1.847   4.881  -1.362  1.00  0.00           C  
HETATM    9  C9  UNL     1       2.344   4.096  -2.514  1.00  0.00           C  
HETATM   10  C10 UNL     1       1.658   2.791  -2.777  1.00  0.00           C  
HETATM   11  C11 UNL     1       0.197   2.925  -3.031  1.00  0.00           C  
HETATM   12  C12 UNL     1      -0.432   1.601  -3.306  1.00  0.00           C  
HETATM   13  C13 UNL     1       0.133   0.926  -4.525  1.00  0.00           C  
HETATM   14  C14 UNL     1      -0.560  -0.380  -4.751  1.00  0.00           C  
HETATM   15  O1  UNL     1      -0.337  -0.998  -5.823  1.00  0.00           O  
HETATM   16  O2  UNL     1      -1.422  -0.925  -3.840  1.00  0.00           O  
HETATM   17  C15 UNL     1      -2.056  -2.180  -4.125  1.00  0.00           C  
HETATM   18  C16 UNL     1      -2.931  -2.588  -2.951  1.00  0.00           C  
HETATM   19  C17 UNL     1      -3.984  -1.561  -2.648  1.00  0.00           C  
HETATM   20  O3  UNL     1      -4.850  -1.356  -3.716  1.00  0.00           O  
HETATM   21  P1  UNL     1      -5.982  -0.204  -3.225  1.00  0.00           P  
HETATM   22  O4  UNL     1      -7.052  -0.975  -2.443  1.00  0.00           O  
HETATM   23  O5  UNL     1      -6.776   0.456  -4.564  1.00  0.00           O1-
HETATM   24  O6  UNL     1      -5.314   1.000  -2.247  1.00  0.00           O  
HETATM   25  C18 UNL     1      -5.844   0.939  -0.945  1.00  0.00           C  
HETATM   26  C19 UNL     1      -5.289   1.989  -0.054  1.00  0.00           C  
HETATM   27  N1  UNL     1      -3.885   1.988   0.153  1.00  0.00           N1+
HETATM   28  C20 UNL     1      -3.630   2.879   1.297  1.00  0.00           C  
HETATM   29  C21 UNL     1      -3.179   2.624  -0.967  1.00  0.00           C  
HETATM   30  C22 UNL     1      -3.268   0.734   0.420  1.00  0.00           C  
HETATM   31  O7  UNL     1      -2.098  -2.728  -1.789  1.00  0.00           O  
HETATM   32  C23 UNL     1      -2.027  -3.925  -1.097  1.00  0.00           C  
HETATM   33  O8  UNL     1      -2.733  -4.870  -1.531  1.00  0.00           O  
HETATM   34  C24 UNL     1      -1.171  -4.123   0.102  1.00  0.00           C  
HETATM   35  C25 UNL     1      -1.340  -5.466   0.714  1.00  0.00           C  
HETATM   36  C26 UNL     1      -0.456  -5.652   1.915  1.00  0.00           C  
HETATM   37  C27 UNL     1       1.018  -5.565   1.619  1.00  0.00           C  
HETATM   38  C28 UNL     1       1.854  -5.755   2.855  1.00  0.00           C  
HETATM   39  C29 UNL     1       1.686  -4.822   3.954  1.00  0.00           C  
HETATM   40  C30 UNL     1       1.969  -3.389   3.892  1.00  0.00           C  
HETATM   41  C31 UNL     1       3.351  -2.911   3.662  1.00  0.00           C  
HETATM   42  C32 UNL     1       4.049  -3.193   2.399  1.00  0.00           C  
HETATM   43  C33 UNL     1       3.390  -2.545   1.192  1.00  0.00           C  
HETATM   44  C34 UNL     1       4.106  -2.873  -0.082  1.00  0.00           C  
HETATM   45  C35 UNL     1       4.169  -4.344  -0.397  1.00  0.00           C  
HETATM   46  C36 UNL     1       4.923  -4.536  -1.707  1.00  0.00           C  
HETATM   47  H1  UNL     1      -1.809   1.301   5.011  1.00  0.00           H  
HETATM   48  H2  UNL     1      -1.618   2.283   3.521  1.00  0.00           H  
HETATM   49  H3  UNL     1      -1.569   0.479   3.449  1.00  0.00           H  
HETATM   50  H4  UNL     1       0.673   0.432   3.651  1.00  0.00           H  
HETATM   51  H5  UNL     1       0.425   1.063   5.287  1.00  0.00           H  
HETATM   52  H6  UNL     1       2.036   2.404   4.089  1.00  0.00           H  
HETATM   53  H7  UNL     1       0.612   3.328   4.696  1.00  0.00           H  
HETATM   54  H8  UNL     1      -0.322   3.404   2.430  1.00  0.00           H  
HETATM   55  H9  UNL     1       0.985   2.404   1.760  1.00  0.00           H  
HETATM   56  H10 UNL     1       2.597   4.217   2.719  1.00  0.00           H  
HETATM   57  H11 UNL     1       1.136   5.098   3.223  1.00  0.00           H  
HETATM   58  H12 UNL     1       0.382   5.400   0.927  1.00  0.00           H  
HETATM   59  H13 UNL     1       2.055   6.010   1.060  1.00  0.00           H  
HETATM   60  H14 UNL     1       1.403   3.231  -0.079  1.00  0.00           H  
HETATM   61  H15 UNL     1       3.030   4.028   0.182  1.00  0.00           H  
HETATM   62  H16 UNL     1       2.496   5.803  -1.284  1.00  0.00           H  
HETATM   63  H17 UNL     1       0.819   5.296  -1.530  1.00  0.00           H  
HETATM   64  H18 UNL     1       2.424   4.699  -3.457  1.00  0.00           H  
HETATM   65  H19 UNL     1       3.419   3.829  -2.289  1.00  0.00           H  
HETATM   66  H20 UNL     1       2.115   2.398  -3.725  1.00  0.00           H  
HETATM   67  H21 UNL     1       1.896   2.061  -2.001  1.00  0.00           H  
HETATM   68  H22 UNL     1      -0.000   3.588  -3.926  1.00  0.00           H  
HETATM   69  H23 UNL     1      -0.355   3.397  -2.184  1.00  0.00           H  
HETATM   70  H24 UNL     1      -1.532   1.699  -3.497  1.00  0.00           H  
HETATM   71  H25 UNL     1      -0.290   0.943  -2.401  1.00  0.00           H  
HETATM   72  H26 UNL     1       1.232   0.750  -4.376  1.00  0.00           H  
HETATM   73  H27 UNL     1       0.005   1.610  -5.376  1.00  0.00           H  
HETATM   74  H28 UNL     1      -2.714  -2.066  -5.012  1.00  0.00           H  
HETATM   75  H29 UNL     1      -1.301  -2.965  -4.298  1.00  0.00           H  
HETATM   76  H30 UNL     1      -3.402  -3.568  -3.116  1.00  0.00           H  
HETATM   77  H31 UNL     1      -3.555  -0.582  -2.397  1.00  0.00           H  
HETATM   78  H32 UNL     1      -4.597  -1.951  -1.810  1.00  0.00           H  
HETATM   79  H33 UNL     1      -6.938   1.200  -1.087  1.00  0.00           H  
HETATM   80  H34 UNL     1      -5.853  -0.064  -0.522  1.00  0.00           H  
HETATM   81  H35 UNL     1      -5.838   1.909   0.922  1.00  0.00           H  
HETATM   82  H36 UNL     1      -5.574   2.987  -0.455  1.00  0.00           H  
HETATM   83  H37 UNL     1      -4.369   3.702   1.288  1.00  0.00           H  
HETATM   84  H38 UNL     1      -3.778   2.251   2.220  1.00  0.00           H  
HETATM   85  H39 UNL     1      -2.592   3.223   1.314  1.00  0.00           H  
HETATM   86  H40 UNL     1      -3.676   3.605  -1.187  1.00  0.00           H  
HETATM   87  H41 UNL     1      -3.216   1.919  -1.817  1.00  0.00           H  
HETATM   88  H42 UNL     1      -2.120   2.746  -0.675  1.00  0.00           H  
HETATM   89  H43 UNL     1      -3.965  -0.107   0.194  1.00  0.00           H  
HETATM   90  H44 UNL     1      -3.066   0.651   1.508  1.00  0.00           H  
HETATM   91  H45 UNL     1      -2.289   0.598  -0.087  1.00  0.00           H  
HETATM   92  H46 UNL     1      -1.468  -3.348   0.865  1.00  0.00           H  
HETATM   93  H47 UNL     1      -0.105  -3.924  -0.121  1.00  0.00           H  
HETATM   94  H48 UNL     1      -2.428  -5.596   0.991  1.00  0.00           H  
HETATM   95  H49 UNL     1      -1.143  -6.257  -0.039  1.00  0.00           H  
HETATM   96  H50 UNL     1      -0.727  -6.635   2.372  1.00  0.00           H  
HETATM   97  H51 UNL     1      -0.685  -4.908   2.720  1.00  0.00           H  
HETATM   98  H52 UNL     1       1.315  -4.767   0.949  1.00  0.00           H  
HETATM   99  H53 UNL     1       1.227  -6.515   1.011  1.00  0.00           H  
HETATM  100  H54 UNL     1       2.871  -6.025   2.529  1.00  0.00           H  
HETATM  101  H55 UNL     1       1.472  -6.772   3.259  1.00  0.00           H  
HETATM  102  H56 UNL     1       0.647  -5.008   4.415  1.00  0.00           H  
HETATM  103  H57 UNL     1       2.343  -5.225   4.815  1.00  0.00           H  
HETATM  104  H58 UNL     1       1.677  -2.968   4.918  1.00  0.00           H  
HETATM  105  H59 UNL     1       1.272  -2.815   3.218  1.00  0.00           H  
HETATM  106  H60 UNL     1       3.977  -3.142   4.572  1.00  0.00           H  
HETATM  107  H61 UNL     1       3.280  -1.761   3.720  1.00  0.00           H  
HETATM  108  H62 UNL     1       4.266  -4.244   2.249  1.00  0.00           H  
HETATM  109  H63 UNL     1       5.067  -2.669   2.483  1.00  0.00           H  
HETATM  110  H64 UNL     1       2.329  -2.766   1.154  1.00  0.00           H  
HETATM  111  H65 UNL     1       3.547  -1.438   1.354  1.00  0.00           H  
HETATM  112  H66 UNL     1       3.547  -2.389  -0.916  1.00  0.00           H  
HETATM  113  H67 UNL     1       5.146  -2.449  -0.036  1.00  0.00           H  
HETATM  114  H68 UNL     1       3.150  -4.763  -0.552  1.00  0.00           H  
HETATM  115  H69 UNL     1       4.669  -4.947   0.382  1.00  0.00           H  
HETATM  116  H70 UNL     1       5.098  -3.551  -2.199  1.00  0.00           H  
HETATM  117  H71 UNL     1       4.372  -5.220  -2.367  1.00  0.00           H  
HETATM  118  H72 UNL     1       5.926  -4.974  -1.485  1.00  0.00           H  
CONECT    1    2   47   48   49
CONECT    2    3   50   51
CONECT    3    4   52   53
CONECT    4    5   54   55
CONECT    5    6   56   57
CONECT    6    7   58   59
CONECT    7    8   60   61
CONECT    8    9   62   63
CONECT    9   10   64   65
CONECT   10   11   66   67
CONECT   11   12   68   69
CONECT   12   13   70   71
CONECT   13   14   72   73
CONECT   14   15   15   16
CONECT   16   17
CONECT   17   18   74   75
CONECT   18   19   31   76
CONECT   19   20   77   78
CONECT   20   21
CONECT   21   22   22   23   24
CONECT   24   25
CONECT   25   26   79   80
CONECT   26   27   81   82
CONECT   27   28   29   30
CONECT   28   83   84   85
CONECT   29   86   87   88
CONECT   30   89   90   91
CONECT   31   32
CONECT   32   33   33   34
CONECT   34   35   92   93
CONECT   35   36   94   95
CONECT   36   37   96   97
CONECT   37   38   98   99
CONECT   38   39  100  101
CONECT   39   40  102  103
CONECT   40   41  104  105
CONECT   41   42  106  107
CONECT   42   43  108  109
CONECT   43   44  110  111
CONECT   44   45  112  113
CONECT   45   46  114  115
CONECT   46  116  117  118
END
Download

SMILES for HMDB0007866 (PC(14:0/14:0))

[H][C@@](COC(=O)CCCCCCCCCCCCC)(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCC
Download

INCHI for HMDB0007866 (PC(14:0/14:0))

InChI=1S/C36H72NO8P/c1-6-8-10-12-14-16-18-20-22-24-26-28-35(38)42-32-34(33-44-46(40,41)43-31-30-37(3,4)5)45-36(39)29-27-25-23-21-19-17-15-13-11-9-7-2/h34H,6-33H2,1-5H3/t34-/m1/s1
Download
View in JSmolView Stereo Labels
Synonyms
ValueSource
1,2-Di-O-tetradecanoyl-sn-glycero-3-phosphocholineChEBI
1,2-Dimyristoyl-GPCChEBI
1,2-Dimyristoyl-L-3-phosphatidylcholineChEBI
1,2-Dimyristoyl-sn-glycero-3-phosphocholineChEBI
1,2-DimyristoylphosphatidylcholineChEBI
1,2-Ditetradecanoyl-sn-glycero-3-phosphocholineChEBI
Dimyristoyl lecithinChEBI
Dimyristoyl phosphatidylcholineChEBI
DimyristoylphosphatidylcholineChEBI
DMPCChEBI
GPC(14:0/14:0)ChEBI
GPC(28:0)ChEBI
PC(28:0)ChEBI
Phosphatidylcholine(14:0/14:0)ChEBI
Phosphatidylcholine(28:0)ChEBI
1,2 Ditetradecanoyl glycero 3 phosphocholineHMDB
1,2-Ditetradecanoyl-glycero-3-phosphocholineHMDB
1,2-Ditetradecyl-glycero-3-phosphocholineHMDB
DMCPHMDB
DimyristoyllecithinHMDB
1,2 Dimyristoyl glycero 3 phosphorylcholineHMDB
1,2 Ditetradecyl glycero 3 phosphocholineHMDB
1,2-Dimyristoyl-glycero-3-phosphorylcholineHMDB
LecithinHMDB
1,2-Dimyristoyl-rac-glycero-3-phosphocholineHMDB
GPCho(28:0)HMDB
GPCho(14:0/14:0)HMDB
1,2-Ditetradecanoyl-rac-glycero-3-phosphocholineHMDB
PC(14:0/14:0)Lipid Annotator, ChEBI
Chemical FormulaC36H72NO8P
Average Molecular Weight677.9325
Monoisotopic Molecular Weight677.499554797
IUPAC Name(2-{[(2R)-2,3-bis(tetradecanoyloxy)propyl phosphono]oxy}ethyl)trimethylazanium
Traditional Name(2-{[(2R)-2,3-bis(tetradecanoyloxy)propyl phosphono]oxy}ethyl)trimethylazanium
CAS Registry Number18194-24-6
SMILES
[H][C@@](COC(=O)CCCCCCCCCCCCC)(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCC
InChI Identifier
InChI=1S/C36H72NO8P/c1-6-8-10-12-14-16-18-20-22-24-26-28-35(38)42-32-34(33-44-46(40,41)43-31-30-37(3,4)5)45-36(39)29-27-25-23-21-19-17-15-13-11-9-7-2/h34H,6-33H2,1-5H3/t34-/m1/s1
InChI KeyCITHEXJVPOWHKC-UUWRZZSWSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as phosphatidylcholines. These are glycerophosphocholines in which the two free -OH are attached to one fatty acid each through an ester linkage.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassGlycerophospholipids
Sub ClassGlycerophosphocholines
Direct ParentPhosphatidylcholines
Alternative Parents
Substituents
  • Diacylglycero-3-phosphocholine
  • Phosphocholine
  • Fatty acid ester
  • Dialkyl phosphate
  • Dicarboxylic acid or derivatives
  • Organic phosphoric acid derivative
  • Phosphoric acid ester
  • Alkyl phosphate
  • Fatty acyl
  • Quaternary ammonium salt
  • Tetraalkylammonium salt
  • Carboxylic acid ester
  • Carboxylic acid derivative
  • Organic oxygen compound
  • Organic nitrogen compound
  • Carbonyl group
  • Organooxygen compound
  • Organonitrogen compound
  • Organic oxide
  • Organopnictogen compound
  • Amine
  • Organic salt
  • Hydrocarbon derivative
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External Descriptors
Ontology
Physiological effect
Health effectOrganoleptic effect
Disposition
Biological locationRoute of exposureSource
Process
Naturally occurring process
Role
Biological roleIndustrial application
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility4.0e-05 g/LALOGPS
logP4.57ALOGPS
logP6.34ChemAxon
logS-7.3ALOGPS
pKa (Strongest Acidic)1.86ChemAxon
pKa (Strongest Basic)-6.7ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area111.19 ŲChemAxon
Rotatable Bond Count36ChemAxon
Refractivity197.46 m³·mol⁻¹ChemAxon
Polarizability82.6 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+269.06530932474
DeepCCS[M-H]-266.23130932474
DeepCCS[M-2H]-300.17530932474
DeepCCS[M+Na]+276.46930932474
AllCCS[M+H]+278.532859911
AllCCS[M+H-H2O]+278.232859911
AllCCS[M+NH4]+278.732859911
AllCCS[M+Na]+278.732859911
AllCCS[M-H]-266.432859911
AllCCS[M+Na-2H]-269.832859911
AllCCS[M+HCOO]-273.632859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
PC(14:0/14:0)[H][C@@](COC(=O)CCCCCCCCCCCCC)(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCC4354.5Standard polar33892256
PC(14:0/14:0)[H][C@@](COC(=O)CCCCCCCCCCCCC)(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCC3896.7Standard non polar33892256
PC(14:0/14:0)[H][C@@](COC(=O)CCCCCCCCCCCCC)(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCC4362.4Semi standard non polar33892256
Spectra

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(14:0/14:0) 10V, Positive-QTOFsplash10-004i-0000009000-bb65a82e598e66ad93ba2017-10-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(14:0/14:0) 20V, Positive-QTOFsplash10-0059-0600009000-ab46b766c037563f8d812017-10-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(14:0/14:0) 40V, Positive-QTOFsplash10-001i-1900303000-096dbc3ddcea51737a5e2017-10-04Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(14:0/14:0) 10V, Positive-QTOFsplash10-001i-0000009000-0079d97febb3635101162021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(14:0/14:0) 20V, Positive-QTOFsplash10-001i-0000009000-5a3bec4fcf551986fbce2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(14:0/14:0) 40V, Positive-QTOFsplash10-0ue9-0202494000-4f45e0e89d33d71298662021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(14:0/14:0) 10V, Positive-QTOFsplash10-004i-0000009000-681b03d960506fdf755a2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(14:0/14:0) 20V, Positive-QTOFsplash10-0059-0600009000-4b4757699f9015f393412021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(14:0/14:0) 40V, Positive-QTOFsplash10-001i-1900303000-8997e12bf49f01c92a712021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(14:0/14:0) 10V, Positive-QTOFsplash10-0udi-0000000900-8fc0d9309c0f16fcac602021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(14:0/14:0) 20V, Positive-QTOFsplash10-0udi-0000001900-36c1a93c28b6ca00d7e52021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(14:0/14:0) 40V, Positive-QTOFsplash10-014k-0900491100-9f29dda8a7d806b45f152021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(14:0/14:0) 10V, Negative-QTOFsplash10-004i-0000009000-23a8f156b4ab890930932021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(14:0/14:0) 20V, Negative-QTOFsplash10-004i-0090107000-78772c87803311fd2a5c2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(14:0/14:0) 40V, Negative-QTOFsplash10-004i-2192010000-81d64300566f10c3bd952021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(14:0/14:0) 10V, Negative-QTOFsplash10-03di-0000000900-0d63162a541c907ab7d22021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(14:0/14:0) 20V, Negative-QTOFsplash10-03di-0010000900-23092bab62b5e5d8d6ab2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - PC(14:0/14:0) 40V, Negative-QTOFsplash10-03i0-0090000900-2416ad715fad2f9c398e2021-09-25Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, H2O, predicted)2022-08-20Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, H2O, predicted)2022-08-20Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, H2O, predicted)2022-08-20Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, H2O, predicted)2022-08-20Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, H2O, predicted)2022-08-20Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, H2O, predicted)2022-08-20Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, H2O, predicted)2022-08-20Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, H2O, predicted)2022-08-20Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, H2O, predicted)2022-08-20Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, H2O, predicted)2022-08-20Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, H2O, predicted)2022-08-20Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, H2O, predicted)2022-08-20Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, H2O, predicted)2022-08-20Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, H2O, predicted)2022-08-20Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, H2O, predicted)2022-08-20Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, H2O, predicted)2022-08-20Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, H2O, predicted)2022-08-20Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, H2O, predicted)2022-08-20Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, H2O, predicted)2022-08-20Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, H2O, predicted)2022-08-20Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Extracellular
  • Membrane
Biospecimen LocationsNot Available
Tissue Locations
  • All Tissues
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Predicted Concentrations
BiospecimenValueOriginal ageOriginal sexOriginal conditionComments
Blood0.045 +/- 0.011 uMAdult (>18 years old)BothNormal (Most Probable)Calculated using MetaboAnalyst
Blood8.450 +/- 1.863 uMAdult (>18 years old)BothNormal (Upper Limit)Calculated using MetaboAnalyst
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDDB09530
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound5459377
PDB IDMC3
ChEBI ID45240
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available

Only showing the first 10 proteins. There are 78 proteins in total.

Show all enzymes and transporters

Enzymes

Enzyme Details
1. Acyl-protein thioesterase 1
General function:
Involved in hydrolase activity
Specific function:
Hydrolyzes fatty acids from S-acylated cysteine residues in proteins such as trimeric G alpha proteins or HRAS. Has depalmitoylating activity and also low lysophospholipase activity.
Gene Name:
LYPLA1
Uniprot ID:
O75608
Molecular weight:
24669.355
Enzyme Details
2. Group XV phospholipase A2
General function:
Involved in phosphatidylcholine-sterol O-acyltransferase activity
Specific function:
Has transacylase and calcium-independent phospholipase A2 activity. Catalyzes the formation of 1-O-acyl-N-acetylsphingosine and the concomitant release of a lyso-phospholipid (By similarity). May have weak lysophospholipase activity.
Gene Name:
PLA2G15
Uniprot ID:
Q8NCC3
Molecular weight:
Not Available
Enzyme Details
3. Calcium-dependent phospholipase A2
General function:
Involved in phospholipase A2 activity
Specific function:
PA2 catalyzes the calcium-dependent hydrolysis of the 2-acyl groups in 3-sn-phosphoglycerides. This isozyme hydrolyzes more efficiently L-alpha-1-palmitoyl-2-oleoyl phosphatidylcholine than L-alpha-1-palmitoyl-2-arachidonyl phosphatidylcholine, L-alpha-1-palmitoyl-2-arachidonyl phosphatidylethanolamine, or L-alpha-1-stearoyl-2-arachidonyl phosphatidylinositol. May be involved in the production of lung surfactant, the remodeling or regulation of cardiac muscle.
Gene Name:
PLA2G5
Uniprot ID:
P39877
Molecular weight:
15674.065
Enzyme Details
4. Group IIF secretory phospholipase A2
General function:
Involved in phospholipase A2 activity
Specific function:
PA2 catalyzes the calcium-dependent hydrolysis of the 2-acyl groups in 3-sn-phosphoglycerides. Hydrolyzes phosphatidylglycerol versus phosphatidylcholine with a 15-fold preference.
Gene Name:
PLA2G2F
Uniprot ID:
Q9BZM2
Molecular weight:
23256.29
Enzyme Details
5. Cytosolic phospholipase A2
General function:
Involved in metabolic process
Specific function:
Selectively hydrolyzes arachidonyl phospholipids in the sn-2 position releasing arachidonic acid. Together with its lysophospholipid activity, it is implicated in the initiation of the inflammatory response.
Gene Name:
PLA2G4A
Uniprot ID:
P47712
Molecular weight:
85210.19
Enzyme Details
6. Phospholipase A2
General function:
Involved in phospholipase A2 activity
Specific function:
PA2 catalyzes the calcium-dependent hydrolysis of the 2-acyl groups in 3-sn-phosphoglycerides.
Gene Name:
PLA2G1B
Uniprot ID:
P04054
Molecular weight:
16359.535
Enzyme Details
7. Group XIIB secretory phospholipase A2-like protein
General function:
Involved in phospholipase A2 activity
Specific function:
Not known; does not seem to have catalytic activity.
Gene Name:
PLA2G12B
Uniprot ID:
Q9BX93
Molecular weight:
Not Available
Enzyme Details
8. Group 10 secretory phospholipase A2
General function:
Involved in phospholipase A2 activity
Specific function:
PA2 catalyzes the calcium-dependent hydrolysis of the 2-acyl groups in 3-sn-phosphoglycerides. Has a powerful potency for releasing arachidonic acid from cell membrane phospholipids. Prefers phosphatidylethanolamine and phosphatidylcholine liposomes to those of phosphatidylserine.
Gene Name:
PLA2G10
Uniprot ID:
O15496
Molecular weight:
18153.04
Enzyme Details
9. Group IIE secretory phospholipase A2
General function:
Involved in phospholipase A2 activity
Specific function:
PA2 catalyzes the calcium-dependent hydrolysis of the 2-acyl groups in 3-sn-phosphoglycerides. Has a preference for arachidonic-containing phospholipids.
Gene Name:
PLA2G2E
Uniprot ID:
Q9NZK7
Molecular weight:
15988.525
Enzyme Details
10. Acyl-protein thioesterase 2
General function:
Involved in hydrolase activity
Specific function:
May hydrolyze fatty acids from S-acylated cysteine residues in proteins such as trimeric G alpha proteins or HRAS. Has lysophospholipase activity (By similarity). Deacylates GAP43.
Gene Name:
LYPLA2
Uniprot ID:
O95372
Molecular weight:
24736.71

Transporters

Enzyme Details
1. Multidrug resistance protein 3
General function:
Involved in ATP binding
Specific function:
Mediates ATP-dependent export of organic anions and drugs from the cytoplasm. Hydrolyzes ATP with low efficiency. Human MDR3 is not capable of conferring drug resistance. Mediates the translocation of phosphatidylcholine across the canalicular membrane of the hepatocyte
Gene Name:
ABCB4
Uniprot ID:
P21439
Molecular weight:
141521.8

Only showing the first 10 proteins. There are 78 proteins in total.

Show all enzymes and transporters