EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C27H48O3 |
| Net Charge | 0 |
| Average Mass | 420.678 |
| Monoisotopic Mass | 420.36035 |
| SMILES | [H][C@@]12C[C@H](O)CC[C@]1(C)[C@@]1([H])CC[C@@]3(C)[C@@]([H])(CC[C@]3([H])[C@H](C)CCC(O)C(C)C)[C@]1([H])[C@H](O)C2 |
| InChI | InChI=1S/C27H48O3/c1-16(2)23(29)9-6-17(3)20-7-8-21-25-22(11-13-27(20,21)5)26(4)12-10-19(28)14-18(26)15-24(25)30/h16-25,28-30H,6-15H2,1-5H3/t17-,18+,19-,20-,21+,22+,23?,24-,25+,26+,27-/m1/s1 |
| InChIKey | VDKSIHRRZLCAGD-RESWAWEDSA-N |
| Roles Classification |
|---|
| Biological Role: | bile acid metabolite Metabolites of bile acids, four-ringed steroid acids formed along the cholesterol degradation pathway. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| 5β-cholestane-3α,7α,24-triol (CHEBI:48700) has parent hydride 5β-cholestane (CHEBI:35517) |
| 5β-cholestane-3α,7α,24-triol (CHEBI:48700) has role bile acid metabolite (CHEBI:48887) |
| 5β-cholestane-3α,7α,24-triol (CHEBI:48700) is a 24-hydroxy steroid (CHEBI:36865) |
| 5β-cholestane-3α,7α,24-triol (CHEBI:48700) is a 3α-hydroxy steroid (CHEBI:36835) |
| 5β-cholestane-3α,7α,24-triol (CHEBI:48700) is a 7α-hydroxy steroid (CHEBI:36843) |
| Incoming Relation(s) |
| (24S)-5β-cholestane-3α,7α,24-triol (CHEBI:63831) is a 5β-cholestane-3α,7α,24-triol (CHEBI:48700) |
| IUPAC Name |
|---|
| 5β-cholestane-3α,7α,24-triol |
| Synonym | Source |
|---|---|
| 5β-cholestan-3α,7α,24-triol | ChEBI |
| Manual Xrefs | Databases |
|---|---|
| LMST04030022 | LIPID MAPS |