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| Product | Description | |
|---|---|---|
| 17-Hydroxyprogesterone acetate | 17-Hydroxyprogesterone acetate. CAS No. 302-23-8. Product ID: 1-01105. Molecular formula: C23H32O4. Mole weight: 372.51. Purity: 0.95. |  |
| 17-Hydroxyprogesterone acetate | 17-Hydroxyprogesterone acetate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 17-HYDROXYPROGESTERONE ACETATE;17-ALPHA-HYDROXYPROGESTERONE 17-ACETATE;17ALPHA-HYDROXYPROGESTERONE ACETATE;17ALPHA-HYDROXY-4-PREGNENE-3,20-DIONE 17-ACETATE;17ALPHA-ACETOXYPROGESTERONE;17-ACETOXYPROGESTERONE;17ALPHA-ACETOXY-4-PREGNENE-3,20-DIONE;ACETIC AC. Product Category: Steroidal Compounds. CAS No. 17308-02-0. Molecular formula: C23H32O4. Mole weight: 372.5. Purity: 95%+. IUPACName: 17-Hydroxypregn-4-ene-3,20-dione acetate. Density: 1.14 g/cm³. Product ID: ACM17308020. Alfa Chemistry ISO 9001:2015 Certified. |  |
| 17a-Hydroxyprogesterone acetate | 17a-Hydroxyprogesterone acetate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: [(8R,9S,10R,13S,14S,17S)-17-acetyl-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl] acetate. Product Category: Heterocyclic Organic Compound. CAS No. 17308-02-2. Molecular formula: C23H32O4. Mole weight: 372.498. Purity: 0.96. IUPACName: 17-Hydroxypregn-4-ene-3,20-dione acetate. Density: 1.14 g/cm³. Product ID: ACM17308022. Alfa Chemistry ISO 9001:2015 Certified. Categories: Prokan, 17-hydroxyprogesterone acetate. | |
| 17-Hydroxyprogesterone Cyclic 20-(Ethylene Acetal) | 17-Hydroxyprogesterone Cyclic 20-(Ethylene Acetal) is an impurity formed in the synthesis of Medroxy Progesterone 17-Acetate, an progesterone related compound used as an injectable contraceptive. Group: Biochemicals. Grades: Highly Purified. CAS No. 70410-76-3. Pack Sizes: 25mg, 100mg. Molecular Formula: C23H34O4. US Biological Life Sciences. |  Worldwide |
| 6a-Chloro-17-acetoxy progesterone | 6a-Chloro-17-acetoxy progesterone. Group: Biochemicals. Alternative Names: (6a)-17-(Acetyloxy)-6-chloropregn-4-ene-3,20-dione; 6a-Chloro-17-hydroxypregn-4-ene-3,20-dione acetate; 6a-Chloro-17-hydroxyprogesterone acetate. Grades: Highly Purified. CAS No. 2477-73-8. Pack Sizes: 10mg, 25mg, 50mg. Molecular Formula: C23H31ClO4. US Biological Life Sciences. | Worldwide |
| Cyproterone acetate | Cyproterone acetate is a synthetic derivative of 17-hydroxyprogesterone, and acts as an androgen receptor antagonist as well as a weak progesterone receptor agonist with weak progestational and glucocorticoid activity. Uses: Androgen antagonists; antineoplastic agents; contraceptive agents, male; progestational hormones, synthetic. Synonyms: Androcur, Cyprostat,Cyproteron, Procur, Cyprone, Cyprohexal, Ciproterona, Cyproteronum, Neoproxil, Siterone. Grade: 0.98. CAS No. 427-51-0. Molecular formula: C24H29ClO4. Mole weight: 416.93766. |  |
| Medroxyprogesterone | analytical standard. Group: Application areaspharma & vet compounds & metabolitespharma & vet compounds & metabolitesapi standardsimpurity standardspharmaceutical toxicology. Alternative Names: 17-Hydroxy-6alpha-methylpregn-4-ene-3,20-dione, NSC 27408, 6alpha-Methyl-17alpha-hydroxypregn-4-ene-3,20-dione,Medroxyprogesterone Acetate Imp. B (EP), 17alpha-Hydroxy-6alpha-methylprogesterone, Pregn-4-ene-3,20-dione, 17-hydroxy-6alpha-methyl- (7CI,8CI), U 8840, Pregn-4-ene-3,20-dione, 17-hydroxy-6-methyl-, (6alpha)-, Medroxyprogesterone Acetate USP Related Compound B, Medroxyprogesterone, 17-Hydroxy-6alpha-methylprogesterone, Medoxyprogesterone, Medroxyprogesterone Acetate USP RC B, Progesterone, 17-hydroxy-6alpha-methyl- (6CI), 6alpha-Methyl-4-pregnen-17alpha-ol-3,20-dione, Medroxyprogesteron, (6alpha)-17-Hydroxy-6-methylpregn-4-ene-3,20-dione, 6alpha-Methyl-17alpha-hydroxyprogesterone, 6alpha-Methyl-17R-hydroxyprogesterone, 6alpha-Methyl-17-hydroxyprogesterone. |  |
| 11Alpha-hydroxyprogesterone | 11Alpha-hydroxyprogesterone. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 11-Hydroxypregn-4-ene-3,20-dione;Pregn-4-ene-3,20-dione, 11alpha-hydroxy-;Progesterone, 11alpha-hydroxy-;U 0384;HYDROXYPROGESTERONE, 11A-;DELTA4-PREGNEN-11ALPHA-OL-3,20-DIONE;4-PREGNEN-11A-OL-3,20-DIONE;4-PREGNEN-11ALPHA-OL-3,20-DIONE. Product Category: Steroidal Compounds. Appearance: white to light beige crystalline powder. CAS No. 80-75-1. Molecular formula: C21H30O3. Mole weight: 330.46. Purity: 0.98. IUPACName: (8S,9S,10R,11R,13S,14S)-17-acetyl-11-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one. Canonical SMILES: CC(=O)C1CCC2C1(CC(C3C2CCC4=CC(=O)CCC34C)O)C. Density: 1.15 g/cm³. ECNumber: 201-306-9. Product ID: ACM80751. Alfa Chemistry ISO 9001:2015 Certified. Categories: 17alpha-hydroxyprogesterone. | |
| 17a-Hydroxy progesterone-21-acetate | 17a-Hydroxy progesterone-21-acetate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: CORTEXOLONE ACETATE; Einecs 211-369-4; Reichstein substance S 21-acetate; 17-Hydroxy-21-acetoxyprogesterone; cortexolone 21-acetate; 11-deoxycortisol 21-acetate; 21-acetoxy-17-hydroxy-pregn-4-ene-3,20-dione; Reichsteins substance S acetate; 17-Hydroxy-21-acetoxy-pregnen-(4)-dion-(3.20); 21-Acetoxy-17a-hydroxyprogesterone; 21-Acetoxy-17-hydroxy-pregn-4-en-3,20-dion; 11-DEOXY-17-HYDROCORTICOSTERONE; 11-deoxycortisone acetate. Product Category: Steroidal Compounds. CAS No. 640-87-9. Molecular formula: C23H32O5. Mole weight: 388.5. Purity: 0.98. IUPACName: [2-[(8R,9S,10R,13S,14S,17R)-17-hydroxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-oxoethyl]acetate. Canonical SMILES: CC(=O)OCC(=O)C1(CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)O. Density: 1.2g/cm³. ECNumber: 211-369-4. Product ID: ACM640879. Alfa Chemistry ISO 9001:2015 Certified. Categories: 21-(Acetyloxy)-17-hydroxypregn-4-ene-3,20-dione. | |
| 17a-Hydroxyprogesterone hexanoate | 17a-Hydroxyprogesterone hexanoate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: [(8R,9S,10R,13S,14S,17R)-17-acetyl-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl] hexanoate. Product Category: Steroidal Compounds. Appearance: White or almost White Crystalline power. CAS No. 630-56-8. Molecular formula: C27H40O4. Mole weight: 428.6. Purity: 0.98. IUPACName: [(8R,9S,10R,13S,14S,17R)-17-acetyl-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl]hexanoate. Canonical SMILES: CCCCCC(=O)OC1(CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(=O)C. Density: 1.1 g/cm³. ECNumber: 211-138-8. Product ID: ACM630568. Alfa Chemistry ISO 9001:2015 Certified. Categories: HYDROXYPROGESTERONE CAPROATE. | |
| 17α-Hydroxyprogesterone 3-(o-carboxymethyl)oxime | 17α-Hydroxyprogesterone 3-(o-carboxymethyl)oxime. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 21-Deoxycortisone; deoxycortisone; 17-hydroxypregn-4-ene-3,11,20-trione; 21-Desoxycortisone; 17-Hydroxy-pregn-4-en-3,11,20-trion. Product Category: Steroidal Compounds. CAS No. 53260-10-9. Molecular formula: C23H33NO5. Mole weight: 403.52. Purity: 0.97. IUPACName: 2-[(E)-[(8R,9S,10R,13S,14S,17R)-17-acetyl-17-hydroxy-10,13-dimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-ylidene]amino]oxyaceticacid. Canonical SMILES: CC(=O)C1(CCC2C1(CCC3C2CCC4=CC(=NOCC(=O)O)CCC34C)C)O. Product ID: ACM53260109. Alfa Chemistry ISO 9001:2015 Certified. | |
| 17α-Hydroxyprogesterone Caproate | 17α-Hydroxyprogesterone Caproate , a synthetic steroidal progestin, is an ester derivative of 17α-hydroxyprogesterone formed from caproic acid used in the treatment of threatened miscarriage, gynecological disorders such as dysmenorrhea, premenstrual synd. Uses: More recently has received the most attention in the prevention of preterm birth. Synonyms: Primolut Depot; HYDROXYPROGESTERONE CAPROATE; [(8R,9S,10R,13S,14S,17R)-17-acetyl-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl] hexanoate. Grade: ≥98%. CAS No. 630-56-8. Molecular formula: C27H40O4. Mole weight: 428.6. | |
| 17α-hydroxyprogesterone deacetylase | A microsomal cytochrome P-450 (heme-thiolate) protein that catalyses two independent reactions at the same active site - the 17-hydroxylation of pregnenolone and progesterone, which is part of glucocorticoid hormones biosynthesis (EC 1.14.14.19), and the conversion of the 17-hydroxylated products via a 17,20-lyase reaction to form androstenedione and 3β-hydroxyandrost-5-en-17-one, leading to sex hormone biosynthesis. The activity of this reaction is dependent on the allosteric interaction of the enzyme with cytochrome b5 without any transfer of electrons from the cytochrome. The enzymes from different organisms differ in their substrate specificity. While the enzyme...son do not accept the former, and the enzyme from guinea pig does not accept the latter. Group: Enzymes. Synonyms: C-17/C-20 lyase; 17α-hydroxyprogesterone acetaldehyde-lyase; CYP17; CYP17A1 (gene name); 17α-hydroxyprogesterone 17,20-lyase. Enzyme Commission Number: EC 1.14.14.32. CAS No. 62213-24-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0930; 17α-hydroxyprogesterone deacetylase; EC 1.14.14.32; 62213-24-5; C-17/C-20 lyase; 17α-hydroxyprogesterone acetaldehyde-lyase; CYP17; CYP17A1 (gene name); 17α-hydroxyprogesterone 17,20-lyase. Cat No: EXWM-0930. |  |
| 18-Hydroxyprogesterone | 18-Hydroxyprogesterone. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 18-Hydroxyprogesterone, EINECS 209-889-1, CID101786, 18-Hydroxypregn-4-ene-3,20-dione, 596-69-0. Product Category: Steroidal Compounds. CAS No. 596-69-0. Molecular formula: C21H30O3. Mole weight: 330.46. Purity: 0.95. IUPACName: (8R,9S,10R,13R,14S,17S)-17-acetyl-13-(hydroxymethyl)-10-methyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one. Canonical SMILES: CC(=O)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)CO. ECNumber: 209-889-1. Product ID: ACM596690. Alfa Chemistry ISO 9001:2015 Certified. Categories: 17-hydroxyprogesterone caproate. | |
| 19-Hydroxyprogesterone | 19-Hydroxyprogesterone. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 4-PREGNEN-19-OL-3,20-DIONE;19-HYDROXYPROGESTERONE;19-HYDROXY-4-PREGNENE-3,20-DIONE;19-hydroxydeoxycorticosterone;19-Hydroxypregn-4-ene-3,20-dione;(8S,9S,10S,13S,14S,17S)-17-acetyl-10-(hydroxymethyl)-13-methyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocycl. Product Category: Steroidal Compounds. CAS No. 596-63-4. Molecular formula: C21H30O3. Mole weight: 330.46. Purity: 0.95. IUPACName: (8S,9S,10S,13S,14S,17S)-17-acetyl-10-(hydroxymethyl)-13-methyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one. Canonical SMILES: CC(=O)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34CO)C. Density: 1.15g/cm³. Product ID: ACM596634. Alfa Chemistry ISO 9001:2015 Certified. Categories: 17-hydroxyprogesterone caproate. | |
| 5β-Pregnan-17-ol-3,20-dione | 5β-Pregnan-17-ol-3,20-dione. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 5-BETA-PREGNAN-17-OL-3,20-DIONE;5BETA-PREGNAN-17ALPHA-OL-3,20-DIONE;5-BETA-DIHYDRO-17-HYDROXYPROGESTERONE;17-alpha-hydroxy-5-beta-pregnane-3,20-dione;17ALPHA-Hydroxy-5B-pregnane-3,20-dione. Product Category: Steroidal Compounds. CAS No. 570-58-1. Molecular formula: C21H32O3. Mole weight: 332.48. Purity: 0.95. IUPACName: (5R,8R,9S,10S,13S,14S,17R)-17-acetyl-17-hydroxy-10,13-dimethyl-2,4,5,6,7,8,9,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-3-one. Canonical SMILES: CC(=O)C1(CCC2C1(CCC3C2CCC4C3(CCC(=O)C4)C)C)O. Product ID: ACM570581. Alfa Chemistry ISO 9001:2015 Certified. | |
| Hydromadinone | Hydromadinone. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Hydromadinone;6alpha-Chloro-17-hydroxyprogesterone;6α-Chloro-17-hydroxypregn-4-ene-3,20-dione;(6S,8R,9S,10R,13S,14S,17R)-17-acetyl-6-chloro-17-hydroxy-10,13-dimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-one;(6S,8R,9S,10R,13S,1. Product Category: Heterocyclic Organic Compound. CAS No. 16469-74-2. Product ID: ACM16469742. Alfa Chemistry ISO 9001:2015 Certified. | |
| ketosteroid monooxygenase | A single FAD-containing enzyme catalyses three types of monooxygenase (Baeyer-Villiger oxidation) reaction. The oxidative esterification of a number of derivatives of progesterone to produce the corresponding 17α-hydroxysteroid 17-acetate ester, such as testosterone acetate, is shown in Reaction (1). The oxidative lactonization of a number of derivatives of androstenedione to produce the 13,17-secoandrosteno-17,13α-lactone, such as testololactone, is shown in Reaction (2). The oxidative cleavage of the 17β-side-chain of 17α-hydroxyprogesterone to produce androstenedione and acetate is shown in Reaction (3). Reaction (1) is also catalysed by EC 1.14.99.4 (p...uctase (20-hydroxylating, side-chain cleaving); androstenedione, NADPH2:oxygen oxidoreductase (17-hydroxylating, lactonizing). Enzyme Commission Number: EC 1.14.13.54. CAS No. 9044-53-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0861; ketosteroid monooxygenase; EC 1.14.13.54; 9044-53-5; steroid-ketone monooxygenase; progesterone, NADPH2:oxygen oxidoreductase (20-hydroxylating, ester-producing); 17α-hydroxyprogesterone, NADPH2:oxygen oxidoreductase (20-hydroxylating, side-chain cleaving); androstenedione, NADPH2:oxygen oxidoreductase (17-hydroxylating, lactonizing). Cat No: EXWM-0861. | |
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