Anodyne| Doisynoestrol | |
|---|---|
 | |
| Molecular structure via molpic | |
| Conformer structure via 3Dmol.js | |
| Molecular formula | C19H22O3[1] |
| Molecular mass | 298.4 g/mol[1] |
| Predicted LogP | 4.6[1] |
| Chirality | racemic[2] |
| Identifiers [] | |
|---|---|
| IUPAC name | (1S,2R)-1-ethyl-7-methoxy-2-methyl-3,4-dihydro-1H-phenanthrene-2-carboxylic acid[1] |
| SMILES | CC[C@H]1C2=C(CC[C@@]1(C)C(=O)O)C3=C(C=C2)C=C(C=C3)OC[1] |
| InChI | InChI=1S/C19H22O3/c1-4-17-16-7-5-12-11-13(22-3)6-8-14(12)15(16)9-10-19(17,2)18(20)21/h5-8,11,17H,4,9-10H2,1-3H3,(H,20,21)/t17-,19+/m0/s1[1] |
| InChIKey | HZZSXUIUESWVSS-PKOBYXMFSA-N[1] |
| Dosing |
|---|
Doisynoestrol
Doisynoestrol (also known as Surestryl, Fenociclina, Fenocycline, Phenocyclin, Surestrine, 3-Methoxy-16,17-secoestra-1,3,5(10),6,8-pentaen-17-oic acid, dl-cis-Bisdehydrodoisynolic acid methyl ether, 2-Phenanthrenecarboxylic acid, 1-ethyl-1,2,3,4-tetrahydro-7-methoxy-2-methyl-, (1R,2S)-rel-, Dehydrofolliculinic acid or 7-Methylbisdehydrodoisynolic acid)
Chemistry
Stereochemistry
(RS)-Doisynoestrol is a racemic mixture of the optical stereoisomers