| Sterol |
| LIPID_ID | ST0203 |
| CHEM_NA | 3-HYDROXYESTRA-1,3,5,7,9-PENTAEN-17-ONE; |
| 11,12,13,14,15,16-HEXAHYDRO-3-HYDROXY-13-ME |
| THYL-17H-CYCLOPENTA[A]PHENANTHREN-17-ONE |
| ; 1,3,5:10,6,8-ESTRA-PENTAEN-3-OL-17-ONE. |
| COMMON_NA | EQUILENIN |
| MOL_FORMULA | C18H18O2 |
| MOL_WT | 266 |
| MELT_PT | 258-259ﾟC(DIL ALC.)(371) |
| BOIL_PT |
| OPT_ROT | [α]16/D=+87ﾟ(12.8mg/1.8ml IN DIOXANE)(371) |
| REFRA_IND |
| DENSITY |
| SOLUBILITY | 0.63g/100ml ALCOHOL(18ﾟC),2.5g/100ml |
| ALCOHOL(BOILING)(371) |
| UV_SPEC | UV MAX(ETHANOL): 231, 270, 282, 292, 325, |
| 340nm(logEmolar=3.85, 3.87, 3.74, 3.58, 3.68, |
| EACH)(372) |
| IR_SPEC |
| NMR_SPEC |
| MS_SPEC |
| NOTE_SPEC |
| SOURCE | ・妊娠馬から分離(371)・1-NAPHTHYLAMINE-6-SULF |
| ONIC ACID(CLEVE'S |
| ACID)から調製された7-METHOXY-1-KETO-1,2,3,4-T |
| ETRAHYDROPHENANTHRENを出発物質として全合成(3 |
| 71/372/373)・1-KETO-1,2,3,4-TETRAHYDROPHENA |
| NTHRENEからの合成(374) |
| ・1-KETO-2-METHYL-7-METHOXY- |
| BIOL_ACTIV | 強いエストロゲン活性を持つ｡(371) |
| NOTE |
| 1998年7月17日 | 10 / 486 ページ |