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| Product | Description | |
|---|---|---|
| Estradiol benzoate | Estradiol benzoate (β-Estradiol 3-benzoate) is a HBx protein inhibitor and inhibits androgen and hepatitis B virus (HBV) transcription, replication. Estradiol benzoate shows antifertility effects, anti- Toxoplasma gondii activity and can improve memory behavior of Ovariectomy (Ovx) female mice [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Natural products. Alternative Names: β-Estradiol 3-benzoate; 17β-Estradiol 3-benzoate. CAS No. 50-50-0. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-B1192. |  |
| Estradiol benzoate | Estradiol benzoate is an estradiol analog which binds to the human, murine and chicken ERα with IC50 of 22-28 nM. Uses: Contraceptive agents, hormonal. Synonyms: Estradiol Benzoate; Oestradiol benzoate; Estradiol monobenzoate; Benzo-Gynoestryl; Ovasterol-B. Grade: >98%. CAS No. 50-50-0. Molecular formula: C25H28O3. Mole weight: 376.49. |  |
| Estradiol benzoate | Estradiol benzoate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: folone; EBZ; Estradiolbenzoate; diogynb; ODB; ESTON-B; β-Estradiol 3-benzoate; Solestro; 17beta-estradiol 3-benzoate; Graafina; Estradiol benzoate; Estradiol Benzoate; MEE. Product Category: Steroidal Compounds. CAS No. 50-50-0. Molecular formula: C25H28O3. Mole weight: 376.49. Purity: 0.98. IUPACName: [(8R,9S,13S,14S,17S)-17-hydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl]benzoate. Canonical SMILES: CC12CCC3C(C1CCC2O)CCC4=C3C=CC(=C4)OC(=O)C5=CC=CC=C5. Density: 1.185g/cm³. ECNumber: 200-043-7. Product ID: ACM50500. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Estradiol Benzoate | Estradiol Benzoate is the synthetic benzoate ester of estradiol, a steroid sex hormone vital to the maintenance of fertility and secondary sexual characteristics in females. As the primary, most potent estrogen hormone produced by the ovaries, estradiol binds to and activates specific nuclear receptors. This agent exhibits mild anabolic and metabolic properties, and increases blood coagulability. Alternative Names: Oestradiol benzoate. Benovocylin. Estradiol 3-benzoate. CAS No. 50-50-0. Product ID: API50500. Molecular formula: C25H28O3. Mole weight: 376.5. EINECS: 200-043-7. SMILES: CC12CCC3C(C1CCC2O)CCC4=C3C=CC(=C4)OC(=O)C5=CC=CC=C5. Appearance: White crystalline powder. Category: Hormone and Endocrine Regulation APIs. |  |
| Estradiol Benzoate | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsapi standardsbritish pharmacopoeiaeuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: Estra-1,3,5(10)-trien-17?-ol, 3-methoxy- (6CI,8CI), 17?-Estradiol 3-methyl ether, 3-Methoxyoestra-1,3,5(10)-trien-17?-ol, Estradiol 3-methyl ether, 3-Methoxyestra-1,3,5(10)-triene-3,17?-diol, 17?-Hydroxy-3-methoxyestra-1,3,5(10)-triene, 3-Methoxyestra-1,3,5(10)-triene-17?-ol, NSC 58851, 3-Methoxyestradiol, 3-Methoxyestra-1,3,5(10)-trien-17?-ol, 3-Methoxy-13?-methyl-1,3,5(10)-gonatrien-17?-ol, 3-Methoxy-17?-hydroxyestra-1,3,5(10)-triene, 3-O-Methylestradiol,Estra-1,3,5(10)-trien-17-ol, 3-methoxy-, (17?)-, (17?)-3-Methoxyestra-1,3,5(10)-trien-17-ol. |  |
| Estradiol Benzoate Impurity E | An impurity of Estradiol. Estradiol? is the major estrogen secreted by the premenopausal ovary. Estrogens direct the development of the female genotype in embryogenesis and at puberty. Synonyms: 17-epi- Estradiol Benzoate. Grade: > 95%. CAS No. 6045-53-0. Molecular formula: C25H28O3. Mole weight: 376.50. | |
| Estradiol benzoate (Standard) | Estradiol benzoate (Standard) is the analytical standard of Estradiol benzoate. This product is intended for research and analytical applications. Estradiol benzoate (β-Estradiol 3-benzoate) is a HBx protein inhibitor and inhibits androgen and hepatitis B virus (HBV) transcription, replication. Estradiol benzoate shows antifertility effects, anti- Toxoplasma gondii activity and can improve memory behavior of Ovariectomy (Ovx) female mice [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. CAS No. 50-50-0. Pack Sizes: 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-B1192R. | |
| ?-Estradiol 3-benzoate | analytical standard. Group: Application areas. | |
| 1,3,5(10)-Estratrien-3,17-beta-diol dibenzoate | 1,3,5(10)-Estratrien-3,17-beta-diol dibenzoate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1,3,5(10)-ESTRATRIEN-3,17-BETA-DIOL DIBENZOATE;17-BETA-ESTRADIOL DIBENZOATE. Product Category: Heterocyclic Organic Compound. CAS No. 4147-13-1. Molecular formula: C32H32O4. Mole weight: 480.59. Purity: 0.96. IUPACName: [(8R,9S,13S,14S,17S)-3-benzoyloxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl] benzoate. Canonical SMILES: CC12CCC3C(C1CCC2OC(=O)C4=CC=CC=C4)CCC5=C3C=CC(=C5)OC(=O)C6=CC=CC=C6. Product ID: ACM4147131. Alfa Chemistry ISO 9001:2015 Certified. | |
| (17α)-Estra-1,3,5(10)-triene-3,17-diol 4-Methyl 3-Benzoate 17-(4-Nitrobenzoate) | (17α)-Estra-1,3,5(10)-triene-3,17-diol 4-Methyl 3-Benzoate 17-(4-Nitrobenzoate) is an intermediate in the synthesis of 4-Methyl-17α-Estradiol wich is a related compound of 17 α-Estradiol (E887995), a biologically active estrogen in human breast cancer cells in tissue culture. 17-?stradiol and its selective receptor, ER-X, are not part of a classical hormone/receptor endocrine system but of a system with important autocrine/paracrine functions in the developing and adult brain. 17-Estradiol may have enormous implications for hormone replacement strategies at the menopause and in the treatment of such neurodegenerative disorders as Alzheimers disease and ischemic stroke. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg, 10mg. Molecular Formula: C33H33NO6. US Biological Life Sciences. |  Worldwide |
| Atrimustine | Atrimustine is a conjugate of chlorambucil and β-estradiol benzoate with the antitumor activity. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Bestrabucil; KM2210. CAS No. 75219-46-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-101604. | |
| Atrimustine | Atrimustine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Bestrabucil, Atrimustine, Atrimustinum [INN-Latin], Atrimustina [INN-Spanish], KM 2210, KM-2210, Estradiol 3-benzoate 17-glycolate, 4-(p-(bis(2-chloroethyl)amino)phenyl)butyrate, Estra-1,3,5(10)-triene-3,17-diol, (17-beta)-, 3-benzoate, 17-((4-(4-(bis(2-chloroethyl)amino)phenyl)-1-oxobutoxy)acetate), Atrimustina, Atrimustinum, Atrimustine [INN], AC1L1EE9, UNII-XC0K09B7K4, C41H47Cl2NO6, 75219-46-4, Estra-1,3,5(10)-triene-3,17-diol (17beta)-, 3-benzoate 17-((4-(4-(bis(2-chloroethyl)amino)phenyl)-1-oxobutoxy)acetate), LS-64756, [(17S)-17-[2-[4-[4-[bis(2-chloroethyl)amino]phenyl]butanoyloxy]acetyl]oxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl] benzoate. Product Category: Heterocyclic Organic Compound. CAS No. 75219-46-4. Molecular formula: C41H47Cl2NO6. Mole weight: 720.72. Purity: 0.96. IUPACName: [(17S)-17-[2-[4-[4-[bis(2-chloroethyl)amino]phenyl]butanoyloxy]acetyl]oxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl] benzoate. Canonical SMILES: CC12CCC3C(C1CCC2OC(=O)COC(=O)CCCC4=CC=C(C=C4)N(CCCl)CCCl)CCC5=C3C=CC(=C5)OC(=O)C6=CC=CC=C6. Product ID: ACM75219464. Alfa Chemistry ISO 9001:2015 Certified. | |
| Drostanolone propionate | Drostanolone propionate is a synthetic anabolic steroid that has been shown to inhibit the growth of renal cell cancer cells. It is used as a component of isotonic solutions for sample preparation in mouse tumor studies. Drostanolone propionate also has a role in the treatment of radiation-induced bowel disease and may be useful in the treatment of other inflammatory bowel diseases such as ulcerative colitis and Crohn's disease. In addition, drostanolone propionate may have a potential drug target in prostate cancer tissues because it inhibits epidermal growth factor (EGF) and is converted to estradiol benzoate, which inhibits EGF-induced proliferation of prostate epithelial cells. CAS No. 521-12-0. Product ID: API521120. SMILES: CCC(=O)O[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC[C@@H]4[C@@]3(C[C@H](C(=O)C4)C)C)C. Category: Active Pharmaceutical Ingredients. | |
| Estradiol Hemihydrate | Estradiol Hemihydrate. Uses: For analytical and research use. Group: Api standards; british pharmacopoeia; european pharmacopoeia (ph. eur.); impurity standards; pharmaceutical toxicology; pharmacopoeial standards. Alternative Names: beta-Estradiol semihydrate,Estradiol Benzoate Imp. A (EP), Estradiol Valerate Imp. A (EP), Estriol Imp. D (EP), beta-Estradiol hemihydrate, Ethinylestradiol Imp. D (EP) as Hemihydrate, Estradiol Valerate Imp. A (EP) as Hemihydrate, Estradiol Hemihydrate, Estra-1,3,5(10)-triene-3,17-diol (17beta)-, hydrate (2:1) (9CI), Estradiol Benzoate Imp. A (EP) as Hemihydrate, Ethinylestradiol Imp. D (EP), Estriol Imp. D (EP) as Hemihydate. CAS No. 35380-71-3. IUPAC Name: (8R,9S,13S,14S,17S)-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,17-diol;hydrate. Molecular formula: 2C18H24O2.H2O. Mole weight: 562.78. Catalog: APS35380713. SMILES: O.C[C@]12CC[C@H]3[C@@H](CCc4cc(O)ccc34)[C@@H]1CC[C@@H]2O.C[C@]56CC[C@H]7[C@@H](CCc8cc(O)ccc78)[C@@H]5CC[C@@H]6O. Format: Neat. | |
| Estradiol valerate | Estradiol valerate is a synthetic ester, specifically the 17-pentanoyl ester, of the natural estrogen, 17β-estradiol. It was introduced in the 1950s, and along with estradiol benzoate and estradiol cypionate, has since become one of the most widely used esters of estradiol. Synonyms: Altadiol; Deladiol; Delestrogen; Estraval; Progynova; Valergen; oestradiol valerate. Grade: 0.98. CAS No. 979-32-8. Molecular formula: C23H32O3. Mole weight: 356.506. | |
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