BE528703A - - Google Patents
Info
- Publication number
- BE528703A BE528703A BE528703DA BE528703A BE 528703 A BE528703 A BE 528703A BE 528703D A BE528703D A BE 528703DA BE 528703 A BE528703 A BE 528703A
- Authority
- BE
- Belgium
- Prior art keywords
- ethers
- testosteron
- desc
- page number
- clms page
- Prior art date
Links
- 150000002170 ethers Chemical class 0.000 description 9
- 235000019441 ethanol Nutrition 0.000 description 8
- MUMGGOZAMZWBJJ-DYKIIFRCSA-N Testostosterone Chemical compound O=C1CC[C@]2(C)[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 MUMGGOZAMZWBJJ-DYKIIFRCSA-N 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 5
- JSPLKZUTYZBBKA-UHFFFAOYSA-N Trioxidane Chemical class OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 4
- 150000003431 steroids Chemical class 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical class CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N acetic acid ethyl ester Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 2
- 238000006136 alcoholysis reaction Methods 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 235000019439 ethyl acetate Nutrition 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- VOXZDWNPVJITMN-ZBRFXRBCSA-N 17β-estradiol Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 VOXZDWNPVJITMN-ZBRFXRBCSA-N 0.000 description 1
- 229960005309 Estradiol Drugs 0.000 description 1
- 229940088597 Hormone Drugs 0.000 description 1
- WRWBCPJQPDHXTJ-DTMQFJJTSA-N Methandriol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@](C)(O)[C@@]1(C)CC2 WRWBCPJQPDHXTJ-DTMQFJJTSA-N 0.000 description 1
- PDMMFKSKQVNJMI-BLQWBTBKSA-N Testosterone propionate Chemical compound C1CC2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H](OC(=O)CC)[C@@]1(C)CC2 PDMMFKSKQVNJMI-BLQWBTBKSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000004718 beta keto acids Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- -1 deoxycorticosteron Chemical compound 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 238000006266 etherification reaction Methods 0.000 description 1
- 238000005755 formation reaction Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 238000001794 hormone therapy Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 150000005217 methyl ethers Chemical group 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 241000894007 species Species 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Steroid Compounds (AREA)
Publications (1)
Publication Number | Publication Date |
---|---|
BE528703A true BE528703A (pt) |
Family
ID=161927
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE528703D BE528703A (pt) |
Country Status (1)
Country | Link |
---|---|
BE (1) | BE528703A (pt) |
-
0
- BE BE528703D patent/BE528703A/fr unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0593601B1 (fr) | Nouvelles compositions a base de derives de la classe des taxanes | |
EP0178442B1 (fr) | Procédé d'enrichissement sélectif en acides gras polyinsaturés delta-6 d'un mélange contenant des acides gras delta-6 et delta-9, fractions enrichies obtenues et leur utilisation | |
EP0507064B1 (fr) | Procédé d'obtention d'un extrait liquide d'antioxydant d'épices | |
EP1213975B1 (fr) | Procede d'extraction des composes lipides furaniques et alcools gras polyhydroxyles de l'avocat | |
EP0271747B1 (fr) | Procédé de fractionnement en continu d'un mélange d'acides gras | |
CA1249995A (fr) | Composes a noyau cyclopropanique, procede de preparation et application a la preparation de derives cyclopropaniques a chaine dihalovinylique | |
EP1246633A2 (fr) | Procede d'extraction des insaponificables des huiles vegetales au moyen de chloro-1-butane | |
CH656639A5 (fr) | Procede pour l'obtention de composes insaponifiables a partir de substances naturelles. | |
CH629792A5 (fr) | Procede de preparation de nouveaux derives de l'oxepane. | |
EP0068055B1 (fr) | Procédé d'obtention d'un extrait stable et désodorisé de sabal serrulatum antiprostatique | |
BE528703A (pt) | ||
FR2510558A1 (fr) | Derives nouveaux d'acide chenodesoxycholique | |
FR2620702A1 (fr) | Procede de preparation d'irones naturelles | |
EP1368012A2 (fr) | Utilisation d'un ou plusieurs shogaol(s) en tant qu'aphrodisiaque | |
EP0097567B1 (fr) | Utilisation d' alkylphénol polyoxyéthyléné comme agents antiséborrhéiques | |
EP1240284A1 (fr) | Procede d'extraction et de fractionnement de matieres grasses par solvant, mettant en oeuvre au moins un hydrofluoroether | |
WO2018091480A1 (fr) | Procédé d'extraction de composés terpéniques | |
BE476705A (pt) | ||
BE569235A (pt) | ||
BE440270A (pt) | ||
CH646983A5 (fr) | Derives acetyleniques chlores de l'androst-4-ene, leur preparation et medicaments les renfermant. | |
BE632212A (pt) | ||
CH598285A5 (en) | Steroid 21-(4-acetamidomethylcyclohexane carboxylates) | |
BE511146A (pt) | ||
CH259818A (fr) | Procédé de préparation d'un extrait aromatique de café. |