Chemical Component Summary | |
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Name | EQUILENIN |
Identifiers | (13S,14S)-3-hydroxy-13-methyl-12,14,15,16-tetrahydro-11H-cyclopenta[a]phenanthren-17-one |
Formula | C18 H18 O2 |
Molecular Weight | 266.334 |
Type | NON-POLYMER |
Isomeric SMILES | C[C@]12CCc3c4ccc(cc4ccc3[C@@H]1CCC2=O)O |
InChI | InChI=1S/C18H18O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h2-5,10,16,19H,6-9H2,1H3/t16-,18-/m0/s1 |
InChIKey | PDRGHUMCVRDZLQ-WMZOPIPTSA-N |
Chemical Details | |
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Formal Charge | 0 |
Atom Count | 38 |
Chiral Atom Count | 2 |
Bond Count | 41 |
Aromatic Bond Count | 11 |
Drug Info: DrugBank
DrugBank ID | DB03515 |
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Name | Equilenin |
Groups | experimental |
Description | Equilenin is an estrogenic steroid produced by horses. It has a total of five double bonds in the A- and B-ring. High concentration of equilenin is found in the urine of pregnant mares. |
Synonyms |
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Categories |
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CAS number | 517-09-9 |
Drug Targets
Name | Target Sequence | Pharmacological Action | Actions |
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Steroid Delta-isomerase | MNLPTAQEVQGLMARYIELVDVGDIEAIVQMYADDATVEDPFGQPPIHGR... | unknown | |
Steroid Delta-isomerase | MNTPEHMTAVVQRYVAALNAGDLDGIVALFADDATVEDPVGSEPRSGTAA... | unknown | |
Cytochrome P450 3A4 | MALIPDLAMETWLLLAVSLVLLYLYGTHSHGLFKKLGIPGPTPLPFLGNI... | unknown | substrate |
Drug Info/Drug Targets: DrugBank 3.0: a comprehensive resource for 'omics' research on drugs. Knox C, Law V, Jewison
T, Liu P, Ly S, Frolkis A, Pon A, Banco K, Mak C, Neveu V, Djoumbou Y, Eisner R, Guo AC, Wishart DS.
Nucleic Acids Res. 2011 Jan; 39 (Database issue):D1035-41. | PMID:21059682
Related Resource References
Resource Name | Reference |
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Pharos | CHEMBL225546 |
PubChem | 444865 |
ChEMBL | CHEMBL225546 |
CCDC/CSD | QQQAMM01 |
COD | 2242124 |