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Epimestrol

Epimestrol structure

Epimestrol 

structure
  • CAS No:

    7004-98-0

  • Formula:

    C19H26O3

  • Chemical Name:

    Epimestrol

  • Synonyms:

    Estra-1,3,5(10)-triene-16,17-diol,3-methoxy-,(16α,17α)-;Estra-1,3,5(10)-triene-16α,17α-diol,3-methoxy-;(16α,17α)-3-Methoxyestra-1,3,5(10)-triene-16,17-diol;NSC 55975;Epimestrol;16α,17α-Dihydroxy-3-methoxyestra-1,3,5(10)-triene;3-Methoxy-17-epiestriol;3-Methoxy)estra-1,3,5(10)-triene-16α,17α-diol;Stimovul;Org 817

Description

Epimestrol is a steroid. It derives from a hydride of an estrane.|A synthetic steroid with estrogenic activity.

Epimestrol Basic Attributes

302.41

302.41

230-278-0

7IVE3SDZ38

55975

G - Genito urinary system and sex hormones

Characteristics

49.7 Ų

159 °C

Drug Information

Compounds that interact with ESTROGEN RECEPTORS in target tissues to bring about the effects similar to those of ESTRADIOL. Estrogens stimulate the female reproductive organs, and the development of secondary female SEX CHARACTERISTICS. Estrogenic chemicals include natural, synthetic, steroidal, or non-steroidal compounds. (See all compounds classified as Estrogens.)

Epimestrol

Epimestrol Use and Manufacturing

Methods of Manufacturing

Reduction of 16-keto-17(α)-hydroxyestratrienol-3-methyl to 16,17- dihydroxyestratrienol-3-methyl ether: A solution of 800 mg of the alpha ketol methyl ether in 100 cc of ethanol and 10 cc of acetic acid was carefully maintained at 40°C (water bath), and 200 g of freshly prepared sodium amalgam (2%) were added in small pieces with efficient swirling. Before all ofthe amalgam had been added, a precipitation of sodium acetate occurred, and at this point an additional 100 cc of 50% acetic acid were added. After all the reducing agent had been added, the mixture was transferred to a separatory funnel with ether and water. The mercury plus aqueous phase was separated, after partitioning, from the ether; the latter may be further washed with water, with 0.5N sodium hydroxide, and again with water to purify the alpha glycol. Evaporation of the ethereal phase yielded a crystalline residue of the isomeric transoid (16(β),17(α)-dihydroxy-steroid-3-methyl ether and cisoid 16(α),17(α)dihydroxy-steroid-3-methyl ether.

Uses

Anterior pituitary activator.

Computed Properties

Molecular Weight:302.4
XLogP3:2.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:302.18819469
Monoisotopic Mass:302.18819469
Topological Polar Surface Area:49.7
Heavy Atom Count:22
Complexity:425
Defined Atom Stereocenter Count:6
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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