850-52-2
Chemical Structure
Altrenogest
Synonym(s): Allyltrenbolone; RU2267
- CAS No.: 850-52-2
- Formula:C21H26O2
- Molecular Weight:310.43
IUPAC Name: (8S,13S,14S,17R)-17-allyl-17-hydroxy-13-methyl-1,2,6,7,8,13,14,15,16,17-decahydro-3H-cyclopenta[a]phenanthren-3-one
InChIKey: VWAUPFMBXBWEQY-ANULTFPQSA-N
SMILES: C[C@]([C@]1(O)CC=C)(C=C2)[C@](CC1)([H])[C@@](CC3)([H])C2=C(CC4)C3=CC4=O
Biological Activity: Altrenogest (Allyltrenbolone) is a progestogen structurally related to veterinary steroid trenbolone.
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Altrenogest | 99.86% | Altrenogest (Allyltrenbolone) is a progestogen structurally related to veterinary steroid trenbolone. | ||||||||||||||||||||
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Altrenogest (Standard) | ≥98% | Altrenogest (Standard) is the analytical standard of Altrenogest. This product is intended for research and analytical applications. Altrenogest (Allyltrenbolone) is a progestogen structurally related to veterinary steroid trenbolone. | ||||||||||||||||||||
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Altrenogest-d5 | Altrenogest-d5 is the deuterium labeled Altrenogest. Altrenogest (Allyltrenbolone) is a progestogen structurally related to veterinary steroid trenbolone. | |||||||||||||||||||||
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Gestrinone (Standard) | ≥98% | Gestrinone (Standard) is the analytical standard of Gestrinone. This product is intended for research and analytical applications. Gestrinone (R2323) is a synthetic steroid hormone used to treat endometriosis. It inhibits leiomyoma cells with an IC50 of 43.67 μM. Gestrinone is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. | ||||||||||||||||||||
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Nomegestrol | Nomegestrol is a potent and orally available progestin, acts as a selective full progesterone receptor agonist, with a Kd of 5.44 nM for rat uterine progesterone receptor, and has moderate antiandrogenic activity and strong antiestrogenic activity. | |||||||||||||||||||||
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Trimegestone | Trimegestone (RU 27987) is an orally active, selective progestogen and PR ligand, with an IC50 of 7.6 nM for hPR, 4.4 nM for rabbit PR, and 3.3 nM for rat PR. Trimegestone induces Alkaline phosphatase activity. Trimegestone exhibits antiandrogenic activity (IC50 = 303 nM). Trimegestone can be used in research related to menopausal symptoms and osteoporosis. | |||||||||||||||||||||
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Norgestrienone | Norgestrienone is an orally active 19‑norprogestogen. Norgestrienone is a synthetic steroid that acts as an agonist of the Progesterone Receptor. Norgestrienone can be used in research related to male hormonal contraception. |
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Demegestone | Demegestone is an agonist of theprogesterone receptor. | |||||||||||||||||||||
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Promegestone | 99.14% | Promegestone (R-5020), a progestin, is a potent progesterone receptor (PR) agonist. Promegestone has the potential for endocrine regulation and cancer research. | ||||||||||||||||||||
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Dienogest (Standard) | 99.87% | Dienogest (Standard) is the analytical standard of Dienogest. This product is intended for research and analytical applications. Dienogest (STS-557) is an orally active and selective progesterone receptor agonist that effectively reduces the gene expression of COX-2, mPGES-1 and aromatase. Dienogest also inhibits the mRNA and protein expression of PGE2 synthase and the activation of NF-κB. Dienogest can be used in studies of endometriosis, menopause and menorrhagia. | ||||||||||||||||||||
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Topterone | Topterone is a topical antiandrogen. | |||||||||||||||||||||
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Testosterone impurity 20 | Testosterone impurity 20 is an impurity of Testosterone. | |||||||||||||||||||||
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6,7-Dehydro Norethindrone | 6,7-Dehydro Norethindrone (6,7-Didehydronorethisterone) (Compound 26) is a Norethisterone (HY-B0554) metabolite. 6,7-Dehydro Norethindrone can be produced by the biotransformation of Norethisterone using Rhizopus microsporus PT2906. 6,7-Dehydro Norethindrone induces Apoptosis, binds to p53 and inhibits the degradation of p53. 6,7-Dehydro Norethindrone selectively exhibits antitumor activity against cervical cancer. | |||||||||||||||||||||
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