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| Formula | C30H50O5 |
| Net Charge | 0 |
| Average Mass | 490.725 |
| Monoisotopic Mass | 490.36582 |
| SMILES | [H][C@@]12C[C@H](O)[C@@]3([H])C(C)(C)[C@@H](O)CC[C@@]34C[C@@]14CC[C@@]1(C)[C@@]2(C)C[C@H](O)[C@]1([H])[C@@]1(C)CC[C@@H](C(C)(C)O)O1 |
| InChI | InChI=1S/C30H50O5/c1-24(2)20(33)8-11-30-16-29(30)13-12-26(5)23(28(7)10-9-21(35-28)25(3,4)34)18(32)15-27(26,6)19(29)14-17(31)22(24)30/h17-23,31-34H,8-16H2,1-7H3/t17-,18-,19-,20-,21-,22-,23-,26+,27-,28+,29-,30+/m0/s1 |
| InChIKey | WENNXORDXYGDTP-UOUCMYEWSA-N |
| Wikipedia |
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| Roles Classification |
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| Biological Role: | metabolite Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites. |
| ChEBI Ontology |
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| Outgoing Relation(s) |
| cycloastragenol (CHEBI:71314) has parent hydride 5α-gonane (CHEBI:35525) |
| cycloastragenol (CHEBI:71314) has role metabolite (CHEBI:25212) |
| cycloastragenol (CHEBI:71314) is a oxolanes (CHEBI:26912) |
| cycloastragenol (CHEBI:71314) is a pentacyclic triterpenoid (CHEBI:25872) |
| cycloastragenol (CHEBI:71314) is a sapogenin (CHEBI:26606) |
| cycloastragenol (CHEBI:71314) is a tetrol (CHEBI:33573) |
| Incoming Relation(s) |
| astragaloside I (CHEBI:91024) has functional parent cycloastragenol (CHEBI:71314) |
| astragaloside II (CHEBI:91026) has functional parent cycloastragenol (CHEBI:71314) |
| astragaloside III (CHEBI:2897) has functional parent cycloastragenol (CHEBI:71314) |
| astragaloside IV (CHEBI:65457) has functional parent cycloastragenol (CHEBI:71314) |
| IUPAC Name |
|---|
| (3β,6α,9β,16β,20R,24S)-20,24-epoxy-9,19-cyclolanostane-3,6,16,25-tetrol |
| Manual Xrefs | Databases |
|---|---|
| Cycloastragenol | Wikipedia |
| Registry Numbers | Sources |
|---|---|
| Reaxys:4238706 | Reaxys |
| CAS:84605-18-5 | ChemIDplus |
| Citations |
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