Anodyne| Equilenin | |
|---|---|
 |
| Esters [] | |
|---|---|
| Equilenin acetate | |
|
| Molecular structure via molpic | |
| Conformer structure via 3Dmol.js | |
| Molecular formula | C18H18O2[1] |
|---|---|
| Molecular mass | 266.3 g/mol[1] |
| Predicted LogP | 3.5[1] |
| Chirality | absolute[2] |
| Identifiers [] | |
|---|---|
| IUPAC name | (13S,14S)-3-hydroxy-13-methyl-12,14,15,16-tetrahydro-11H-cyclopenta[a]phenanthren-17-one[1] |
| SMILES | C[C@]12CCC3=C([C@@H]1CCC2=O)C=CC4=C3C=CC(=C4)O[1] |
| 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[1] |
| InChIKey | PDRGHUMCVRDZLQ-WMZOPIPTSA-N[1] |
| Dosing |
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Equilenin
Equilenin (also known as Equilenine, d-Equilenin, (+)-Equilenin, 3-Hydroxyestra-1,3,5(10),6,8-pentaen-17-one, 3-Hydroxyestra-1,3,5,7,9-pentaen-17-one, Equilenina, CCRIS 9075, 6,8-didehydroestrone, 4-08-00-01420 or 3-Hydroxyoestra-1,3,5(10),6,8-pentaen-17-one) is a substance of the steroid class.
Chemistry
Equilenin is typically found in the form of its acetate ester.
Stereochemistry
Equilenin is a absolute mixture