Structure Database (LMSD)

O P P OH O OH O O O HO S NH 2 N N N O N O P OH HO O O O OH N H O NH
Common Name
Elaidoyl-CoA
Systematic Name
9E-octadecanoyl-CoA
Synonyms
  • trans-9-octadecenoyl-CoA
LM ID
LMFA07050492
Formula
Exact Mass
Calculate m/z
1031.360534
Sum Composition
Status
Active

Main

Classification

String Representations

InChiKey (Click to copy)
XDUHQPOXLUAVEE-MBEFLBOUSA-N
InChi (Click to copy)
InChI=1S/C39H68N7O17P3S/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-30(48)67-23-22-41-29(47)20-21-42-37(51)34(50)39(2,3)25-60-66(57,58)63-65(55,56)59-24-28-33(62-64(52,53)54)32(49)38(61-28)46-27-45-31-35(40)43-26-44-36(31)46/h11-12,26-28,32-34,38,49-50H,4-10,13-25H2,1-3H3,(H,41,47)(H,42,51)(H,55,56)(H,57,58)(H2,40,43,44)(H2,52,53,54)/b12-11+/t28-,32-,33-,34+,38-/m1/s1
SMILES (Click to copy)
C(SCCNC(=O)CCNC([C@H](O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@@H]1[C@@H](OP(=O)(O)O)[C@@H](O)[C@@H](O1)N1C=NC2C(N)=NC=NC1=2)=O)(CCCCCCC/C=C/CCCCCCCC)=O

References

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Rattus norvegicus (#10116)
Mammalia (#40674)
Leaky beta-oxidation of a trans-fatty acid: incomplete beta-oxidation of elaidic acid is due to the accumulation of 5-trans-tetradecenoyl-CoA and its hydrolysis and conversion to 5-trans-tetradecenoylcarnitine in the matrix of rat mitochondria.,
J Biol Chem, 2004
Pubmed ID: 15466478

Other Databases

CHEBI ID
PubChem CID
SwissLipids ID

Calculated Physicochemical Properties

Heavy Atoms 67
Rings 3
Aromatic Rings 2
Rotatable Bonds 35
Van der Waals Molecular Volume 907.69
Topological Polar Surface Area 365.70
Hydrogen Bond Donors 9
Hydrogen Bond Acceptors 24
logP 7.95
Molar Refractivity 250.50

Reactions

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Reactions graph legend

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Created at
13th Nov 2023
Updated at
13th Nov 2023