Structure Database (LMSD)
Common Name
Cholestenoic acid
Systematic Name
3β-Hydroxycholest-5-en-25R-26-oic acid
Synonyms
- 3beta-hydroxy-5-cholestenoic acid
- hydroxycholestenoic acid
LM ID
LMST04030072
Formula
Exact Mass
Calculate m/z
416.329045
Sum Composition
Status
Active
3D model of Cholestenoic acid
Please note: Where there are chiral atoms but the stereochemistry is undefined, the 3D model takes an arbitrary conformation
Main
Classification
Category
Main Class
Sub Class
String Representations
InChiKey (Click to copy)
WVXOMPRLWLXFAP-KQOPCUSDSA-N
InChi (Click to copy)
InChI=1S/C27H44O3/c1-17(6-5-7-18(2)25(29)30)22-10-11-23-21-9-8-19-16-20(28)12-14-26(19,3)24(21)13-15-27(22,23)4/h8,17-18,20-24,28H,5-7,9-16H2,1-4H3,(H,29,30)/t17-,18-,20+,21+,22-,23+,24+,26+,27-/m1/s1
SMILES (Click to copy)
C1[C@]2(C)[C@@]3([H])CC[C@]4(C)[C@@]([H])([C@]([H])(C)CCC[C@@]([H])(C)C(O)=O)CC[C@@]4([H])[C@]3([H])CC=C2C[C@@H](O)C1
References
Calculated Physicochemical Properties
Heavy Atoms
30
Rings
4
Aromatic Rings
0
Rotatable Bonds
6
Van der Waals Molecular Volume
447.31
Topological Polar Surface Area
57.53
Hydrogen Bond Donors
2
Hydrogen Bond Acceptors
3
logP
6.74
Molar Refractivity
121.53
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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![Reactions graph legend](https://lipidmaps.org/assets/images/reactions/Legend_LMSD.png)
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Created at
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Updated at
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