71-58-9
Chemical Structure
Medroxyprogesterone acetate
Synonym(s): Medroxyprogesterone 17-acetate; Farlutin
- CAS No.: 71-58-9
- Formula:C24H34O4
- Molecular Weight:386.52
IUPAC Name: (6S,8R,9S,10R,13S,14S,17R)-17-acetyl-6,10,13-trimethyl-3-oxo-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl acetate
InChIKey: PSGAAPLEWMOORI-PEINSRQWSA-N
SMILES: CC(O[C@@]([C@]12C)(CC[C@@]1([H])[C@@](C[C@H](C)C3=CC4=O)([H])[C@]([C@]3(CC4)C)([H])CC2)C(C)=O)=O
Biological Activity: Medroxyprogesterone acetate is a widely used synthetic steroid by its interaction with progesterone, androgen and glucocorticoid receptors[1].
| Cat. No. | Nom du produit | Pureté | Description | Pricing | |||||||||||||||||||
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Medroxyprogesterone acetate | 99.88% | Medroxyprogesterone acetate is a widely used synthetic steroid by its interaction with progesterone, androgen and glucocorticoid receptors. | ||||||||||||||||||||
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Medroxyprogesterone acetate (Standard) | 99.18% | Medroxyprogesterone acetate (Standard) is the analytical standard of Medroxyprogesterone acetate. This product is intended for research and analytical applications. Medroxyprogesterone acetate is a widely used synthetic steroid by its interaction with progesterone, androgen and glucocorticoid receptors. | ||||||||||||||||||||
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Medroxyprogesterone acetate-d3 | 98.50% | Medroxyprogesterone acetate-d3 is deuterium labeled Medroxyprogesterone acetate. Medroxyprogesterone acetate is a widely used synthetic steroid by its interaction with progesterone, androgen and glucocorticoid receptors. | ||||||||||||||||||||
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Medroxyprogesterone acetate-d7 | Medroxyprogesterone acetate-d7 (Medroxyprogesterone 17-acetate-d7) is the deuterium labeled Medroxyprogesterone acetate (HY-B0469) . Medroxyprogesterone acetate is a widely used synthetic steroid by its interaction with progesterone, androgen and glucocorticoid receptors. | |||||||||||||||||||||
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Norgestomet | 98.16% | Norgestomet is a synthetic 19-nortestosterone-derived progestin analog specifically used for estrus synchronization and reproductive regulation in cattle. Norgestomet reduces the incidence of short luteal phases in postpartum lactating beef cattle, enhances luteal function, and increases the pregnancy rate of timed breeding. Norgestomet suppresses estrus during embryo implantation, synchronizes the timing of estrus resumption, and improves the calving rate of first timed artificial insemination in pubertal beef heifers. | ||||||||||||||||||||
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Flumedroxone acetate | Flumedroxone acetate is an active compound. | |||||||||||||||||||||
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Megestrol acetate (Standard) | 98.46% | Megestrol acetate (Standard) is the analytical standard of Megestrol acetate. This product is intended for research and analytical applications. Megestrol acetate is a synthetic and orally active progesteronal agent. Megestrol acetate is effective as an appetite stimulant for wasting syndromes such as cachexia. Megestrol acetate decreases nuclear and cytosol androgen receptors human BPH tissue. Megestrol acetate has the potential for HIV study and downregulates autophagic catabolic pathway. |
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Medroxyprogesterone | 98.82% | Medroxyprogesterone (17α-Hydroxy-6α-methylprogesterone) is a synthetic human variant of progesterone that is a progesterone receptor agonist with oral activity. Medroxyprogesterone can induce cell proliferation through the PI3K/Akt signaling pathway. Medroxyprogesterone has an inhibitory effect on atherosclerosis in mice. The progesterone agonist activity of Medroxyprogesterone is less effective than Medroxyprogesterone acetate (HY-B0469). | ||||||||||||||||||||
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Hydroxyprogesterone caproate | 99.29% | Hydroxyprogesterone caproate (17α-Hydroxyprogesterone hexanoate; 17α-Hydroxyprogesterone caproate) is a progesterone receptor (progesterone receptor) ligand and steroid hormone transcription inhibitor. Hydroxyprogesterone caproate downregulates estrogen receptors in target tissues and activates their metabolic pathways, and exhibits equivalent affinity for progesterone receptor A and progesterone receptor B. Hydroxyprogesterone caproate shows no consistent teratogenicity or developmental toxicity in rat, mouse and monkey models, but induces resorption or abortion in rhesus monkeys at human-equivalent doses. Hydroxyprogesterone caproate promotes the production of TNF-α in lipopolysaccharide-stimulated whole blood from non-pregnant women. Hydroxyprogesterone caproate can be used in scientific research related to preterm birth. | ||||||||||||||||||||
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Chlormadinone acetate | 98.0% | Chlormadinone acetate is a progestogen with potent progestogenic activity and antiandrogenic effects. Chlormadinone acetate acts on glucocorticoid receptor, progesterone receptor, androgen receptor, and GABAA receptor. Chlormadinone acetate induces endometrial proliferation in estrogen-pretreated rabbits, inhibits testosterone-stimulated growth of the prostate and seminal vesicles in castrated rats, and reduces the thymus and adrenal weights in juvenile rats. Chlormadinone acetate is applicable to research related to diseases such as depression and reproductive metabolic disorders. | ||||||||||||||||||||
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17α-Hydroxyprogesterone acetate (Standard) | ≥98% | 17α-Hydroxyprogesterone acetate (Standard) is the analytical standard of 17α-Hydroxyprogesterone acetate. This product is intended for research and analytical applications. 17α-Hydroxyprogesterone acetate possesses progestational activity. 17α-Hydroxyprogesterone acetate has antiinflammatory effects at the murine maternal-fetal interface. | ||||||||||||||||||||
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Medroxyprogesterone acetate impurity 4 | Medroxyprogesterone acetate impurity 4 is an impurity of Medroxyprogesterone acetate. | |||||||||||||||||||||
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Medroxyprogesterone acetate impurity 1 | Medroxyprogesterone acetate impurity 1 is an impurity of Medroxyprogesterone acetate. | |||||||||||||||||||||
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Medroxyprogesterone acetate impurity 3 | Medroxyprogesterone acetate impurity 3 is an impurity of Medroxyprogesterone acetate. | |||||||||||||||||||||
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