Structure Database (LMSD)
Common Name
3S-hydroxy-5Z-octenoyl-CoA
Systematic Name
3S-hydroxy-5Z-octenoyl-CoA
Synonyms
LM ID
LMFA07050432
Formula
Exact Mass
Calculate m/z
907.198949
Sum Composition
Status
Active (generated by computational methods)
No other lipid differing only in stereochemistry/bond geometry found
3D model of 3S-hydroxy-5Z-octenoyl-CoA
Please note: Where there are chiral atoms but the stereochemistry is undefined, the 3D model takes an arbitrary conformation
Classification
Reactions
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Reactions are shown if the E.C. number of the enzyme catalysing it is annotated in the UniProt database for a species belonging to the selected taxonomic class.
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String Representations
InChiKey (Click to copy)
PFTPZODTFGWKLR-UYNKFZPLSA-N
InChi (Click to copy)
InChI=1S/C29H48N7O18P3S/c1-4-5-6-7-17(37)12-20(39)58-11-10-31-19(38)8-9-32-27(42)24(41)29(2,3)14-51-57(48,49)54-56(46,47)50-13-18-23(53-55(43,44)45)22(40)28(52-18)36-16-35-21-25(30)33-15-34-26(21)36/h5-6,15-18,22-24,28,37,40-41H,4,7-14H2,1-3H3,(H,31,38)(H,32,42)(H,46,47)(H,48,49)(H2,30,33,34)(H2,43,44,45)/b6-5-/t17-,18+,22+,23+,24-,28+/m0/s1
SMILES (Click to copy)
[C@@H]1([C@H](O)[C@H](OP(=O)(O)O)[C@@H](COP(O)(=O)OP(O)(=O)OCC(C)([C@@H](O)C(=O)NCCC(=O)NCCSC(C[C@@H](O)C/C=C\CC)=O)C)O1)N1C=NC2C(N)=NC=NC1=2
Other Databases
PubChem CID
Calculated Physicochemical Properties
Heavy Atoms
58
Rings
3
Aromatic Rings
2
Rotatable Bonds
25
Van der Waals Molecular Volume
743.48
Topological Polar Surface Area
385.93
Hydrogen Bond Donors
10
Hydrogen Bond Acceptors
25
logP
3.31
Molar Refractivity
206.23
Admin
Created at
15th Sep 2021
Updated at
25th Apr 2022