Structure Database (LMSD)

Common Name
7alpha,12alpha,(25R)26-Trihydroxy-5beta-cholestan-3-one
Systematic Name
7α,12α,(25R)26-Trihydroxy-5β-cholestan-3-one
Synonyms
LM ID
LMST04030246
Status
Active
Exact Mass
Calculate m/z
434.33961
Formula
Abbrev


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MDLMOL SDF CSV TSV
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Main

Classification

String Representations

InChiKey (Click to copy)
UCVRZTRGVBWBPR-QGLFLVSTSA-N
InChi (Click to copy)
InChI=1S/C27H46O4/c1-16(15-28)6-5-7-17(2)20-8-9-21-25-22(14-24(31)27(20,21)4)26(3)11-10-19(29)12-18(26)13-23(25)30/h16-18,20-25,28,30-31H,5-15H2,1-4H3/t16-,17-,18+,20-,21+,22+,23-,24+,25+,26+,27-/m1/s1
SMILES (Click to copy)
[C@]12([C@H](O)C[C@]3([H])CC(=O)CC[C@]3(C)[C@@]1([H])C[C@H](O)[C@]1(C)[C@@]([H])([C@@](C)([H])CCC[C@@H](C)CO)CC[C@@]21[H])[H]

References

Reference
Oxysterols as lipid mediators: Their biosynthetic genes, enzymes and metabolites.
Prostaglandins Other Lipid Mediat, 2020
DOI: 10.1016/j.prostaglandins.2019.106381
PMID: 31698146

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Homo sapiens (#9606)
Mammalia (#40674)
Oxysterols as lipid mediators: Their biosynthetic genes, enzymes and metabolites.,
Prostaglandins Other Lipid Mediat, 2020
Pubmed ID: 31698146

Other Databases

PubChem CID

Calculated Physicochemical Properties

Heavy Atoms 31
Rings 4
Aromatic Rings 0
Rotatable Bonds 6
Van der Waals Molecular Volume 458.74
Topological Polar Surface Area 77.76
Hydrogen Bond Donors 3
Hydrogen Bond Acceptors 4
logP 5.45
Molar Refractivity 123.78

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Created at
26th Jan 2021
Updated at
26th Jan 2021