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Megestrol

Megestrol Structure
CAS No.
3562-63-8
Chemical Name:
Megestrol
Synonyms
C07120;Megestro;MEGESTROL;Megestrol USP/EP/BP;megestrol solution,100ppm;Megestrol acetate EP Impurity B;Metesterone acetate EP impurity B;4,6-PREGNADIEN-6-METHYL-17-OL-3,20-DIONE;Megestrol (base and/or unspecified salts);20-dione,17-hydroxy-6-methyl-pregna-6-diene-3
CBNumber:
CB5465978
Molecular Formula:
C22H30O3
Molecular Weight:
342.47
MOL File:
3562-63-8.mol
MSDS File:
SDS
Modify Date:
2023/5/19 17:20:51

Megestrol Properties

Melting point 207-208 °C(Solv: ethyl ether (60-29-7); acetone (67-64-1))
Boiling point 500.4±50.0 °C(Predicted)
Density 1.15±0.1 g/cm3(Predicted)
storage temp. Refrigerator
solubility Chloroform (Slightly), Methanol (Slightly)
form Solid
pka 13.00±0.70(Predicted)
color White to Off-White
CAS DataBase Reference 3562-63-8(CAS DataBase Reference)

Megestrol Chemical Properties,Uses,Production

Chemical Properties

White Solid

Uses

Megestrol is an orally active progestogen. Megestrol is used in combinations as oral contraceptive and as antineoplastic agent.

Indications

As a representitive of the compounds of the class of progestins, this drug is used for various forms of cancer, in particular cancer of the breast, kidneys, and others.

Definition

ChEBI: A 3-oxo Delta4-steroid that is pregna-4,6-diene-3,20-dione substituted by a hydroxy group at position 17.

World Health Organization (WHO)

Megestrol acetate, a synthetic progestogen, was introduced in the early 1960s as a component in oral contraceptive preparations. In 1967, as a result of new regulations required by the United States Food and Drug Administration, megestrol acetate was submitted to long-term toxicity studies and by the early 1970s it was shown to be associated with an increased incidence of mammary tumours in beagle bitches which led to its withdrawal by several regulatory authorities. Subsequently the validity of the beagle bitch model as a predictor of carcinogenicity of steroid contraceptives has been contested by many national regulatory authorities and megestrol remains available in some countries for contraceptive purposes. In other countries its use is restricted to anticancer treatment. (Reference: (WHODI) WHO Drug Information, 1-3, 5-7, 1984)

Megestrol Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 152)Suppliers
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17-hydroxy-6-methylpregna-4,6-diene-3,20-dione 20-dione,17-hydroxy-6-methyl-pregna-6-diene-3 4,6-PREGNADIEN-6-METHYL-17-OL-3,20-DIONE 17-ALPHA-HYDROXY-6-METHYL-4,6-PREGNADIENE-3,20-DIONE MEGESTROL 17-alpha-hydroxy-6-methylpregna-4,6-diene-3,20-dione Megestrol (base and/or unspecified salts) C07120 megestrol solution,100ppm (8R,9S,10R,13S,14S,17R)-17-Acetyl-17-hydroxy-6,10,13-trimethyl-8,9,10,11,12,13,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3(2H)-one Megestrol acetate EP Impurity B Megestrol Acetate Impurity 2(Megestrol Acetate EP Impurity B)(Megestrol) Megestro Pregna-4,6-diene-3,20-dione, 17-hydroxy-6-methyl- Megestrol Acetate Impurity 2(Megestrol Acetate EP Impurity B) Metesterone acetate EP impurity B Megestrol USP/EP/BP 3562-63-8 Hormone Drugs Intermediates & Fine Chemicals Pharmaceuticals Steroids 3562-63-8