medroxyprogesterone structure
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Common Name | medroxyprogesterone | ||
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CAS Number | 520-85-4 | Molecular Weight | 344.488 | |
Density | 1.1±0.1 g/cm3 | Boiling Point | 488.0±45.0 °C at 760 mmHg | |
Molecular Formula | C22H32O3 | Melting Point | 220-223.5ºC | |
MSDS | Chinese USA | Flash Point | 263.0±25.2 °C | |
Symbol |
GHS08 |
Signal Word | Warning |
Use of medroxyprogesteroneMedroxyprogesterone is a progestin, a synthetic variant of the human hormone progesterone and a potent progesterone receptor agonist.Target: Progesterone ReceptorMedroxyprogesterone (MP), is a steroidal progestin drug which was never marketed for use in humans. An acylated derivative, medroxyprogesterone acetate (MPA), is clinically used as a pharmaceutical medicine. Compared to MPA, MP is over two orders of magnitude less potent as a progestogen. As such, MP itself is not used clinically, though it has seen limited use in veterinary medicine under the trade name Controlestril in France. In addition, it is an metabolite of MPA [1]. |
Name | medroxyprogesterone |
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Synonym | More Synonyms |
Description | Medroxyprogesterone is a progestin, a synthetic variant of the human hormone progesterone and a potent progesterone receptor agonist.Target: Progesterone ReceptorMedroxyprogesterone (MP), is a steroidal progestin drug which was never marketed for use in humans. An acylated derivative, medroxyprogesterone acetate (MPA), is clinically used as a pharmaceutical medicine. Compared to MPA, MP is over two orders of magnitude less potent as a progestogen. As such, MP itself is not used clinically, though it has seen limited use in veterinary medicine under the trade name Controlestril in France. In addition, it is an metabolite of MPA [1]. |
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Related Catalog | |
References |
Density | 1.1±0.1 g/cm3 |
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Boiling Point | 488.0±45.0 °C at 760 mmHg |
Melting Point | 220-223.5ºC |
Molecular Formula | C22H32O3 |
Molecular Weight | 344.488 |
Flash Point | 263.0±25.2 °C |
Exact Mass | 344.235138 |
PSA | 54.37000 |
LogP | 3.38 |
Vapour Pressure | 0.0±2.8 mmHg at 25°C |
Index of Refraction | 1.554 |
Storage condition | Refrigerator |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Symbol |
GHS08 |
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Signal Word | Warning |
Hazard Statements | H361 |
Precautionary Statements | P280 |
Personal Protective Equipment | Eyeshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges |
Hazard Codes | Xn |
Risk Phrases | 48-63-68 |
Safety Phrases | 22-24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
RTECS | TU5300000 |
Precursor 6 | |
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DownStream 3 | |
Luteolin inhibits progestin-dependent angiogenesis, stem cell-like characteristics, and growth of human breast cancer xenografts.
Springerplus 4 , 444, (2015) Clinical trials and epidemiological evidence have shown that combined estrogen/progestin hormone replacement therapy, but not estrogen therapy alone, increases breast cancer risk in post-menopausal wo... |
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Development of a suspect and non-target screening approach to detect veterinary antibiotic residues in a complex biological matrix using liquid chromatography/high-resolution mass spectrometry.
Rapid Commun. Mass Spectrom. 29 , 2361-73, (2015) Swine manure can contain a wide range of veterinary antibiotics, which could enter the environment via manure spreading on agricultural fields. A suspect and non-target screening method was applied to... |
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Anti-Human Immunodeficiency Virus Activity of Thiol-Ene Carbosilane Dendrimers and Their Potential Development as a Topical Microbicide.
J. Biomed. Nanotechnol. 11 , 1783-98, (2015) The concept of a "microbicide" was born out of the lack of a vaccine against HIV and the difficulty of women in ensuring the use of preventive prophylaxis by their partners, especially in developing c... |
Medroxyprogesteron |
Medroxyprogesteronum |
Hydroxymethylprogesterone |
MFCD00069474 |
17α-Hydroxy-6α-methylprogesterone |
Medroxy Progesterone |
17-Hydroxy-6α-methylprogesterone |
Medrossiprogesterone |
17alpha-Hydroxy-6alpha-methylprogesterone |
(6a)-17-Hydroxy-6-methylpregn-4-ene-3,20-dione |
17-Hydroxy-6a-methylprogesterone |
Medroxiprogesterone |
17a-Hydroxy-6a-methylprogesterone |
17-Hydroxy-6alpha-methylprogesterone |
6a-Methyl-17a-hydroxyprogesterone |
6α-Methyl-17α-hydroxyprogesterone |
Farlutal |
17α-Hydroxy-6α-methylpregn-4-ene-3,20-dione |
EINECS 208-298-6 |
(6α)-17-Hydroxy-6-methylpregn-4-ene-3,20-dione |
Pregn-4-ene-3,20-dione, 17-hydroxy-6α-methyl- |
medroxyprogesterone |
(6S,8R,9S,10R,13S,14S,17R)-17-acetyl-17-hydroxy-6,10,13-trimethyl-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-3-one |
Pregn-4-ene-3,20-dione, 17-hydroxy-6-methyl-, (6α)- |
Medroxiprogesteronum |
Pregn-4-ene-3,20-dione, 17α-hydroxy-6α-methyl- |
Medroxyprogesterone Base |