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Mepitiostane

CAS No.
21362-69-6
Chemical Name:
Mepitiostane
Synonyms
10364S;Mepitiostane;Mepitiostane (Contains ~15% 3α,4α-Epithio isomer);2a,3a-Epithio-17b-(cyclopentylmethoxy)-5a-androstane;2α,3α-Epithio-17β-(cyclopentylMethoxy)-5α-androstane;2α,3α-Epithio-17β-(1-Methoxycyclopentyloxy)-5α-androstane;2a,3a-Epithio-17b-(1-methoxycyclopentyloxy)-5a-androstane;2,3-Epithio-1H-cyclopenta[a]phenanthrene, androstane deriv.;2a,3a-Epithio-5a-androstan-17b-yl 1-methoxycyclopentyl ether;2α,3α-Epithio-5α-androstan-17β-yl 1-Methoxycyclopentyl Ether
CBNumber:
CB81179125
Molecular Formula:
C25H40O2S
Molecular Weight:
404.65
MDL Number:
MFCD00866517
MOL File:
21362-69-6.mol
Last updated:2023-05-15 10:44:01

Mepitiostane Properties

Melting point 98-101°
alpha D20 +22.5 ±0.5° (c = 1 in chloroform)
Boiling point 496.21°C (rough estimate)
Density 0.9998 (rough estimate)
refractive index 1.5200 (estimate)
solubility Chloroform (Slightly), Ethyl Acetate (Slightly)
form Solid
color White to Off-White
Stability Acid Sensitive
FDA UNII O00404969K

Mepitiostane price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
American Custom Chemicals Corporation SHG0006892 MEPITIOSTANE 95.00% 21362-69-6 10MG $2425.5 2021-12-16 Buy
Product number Packaging Price Buy
SHG0006892 10MG $2425.5 Buy

Mepitiostane Chemical Properties,Uses,Production

Originator

Thioderon,Shionogi,Japan,1979

Uses

An orally active anabolic and androgenic steroid. It is a steroidal anti-estrogen with anti-mammary tumor activity.

Definition

ChEBI: Mepitiostane is an organic molecular entity.

Manufacturing Process

A mixture of 1.759 g of 2α,3α-epithio-5α-androstan-17β-ol, 2.3 ml of 1- methoxycyclopentene, 20 mg of pyridine salt of p-toluenesulfonic acid and 20 ml of t-butanol is stirred for 4 hours at room temperature. The reaction mixture is poured into an aqueous solution of sodium carbonate and the whole extracted with dichloromethane. The extract is dried over anhydrous sodium sulfate and evaporated to remove solvent. Purification of the residue by chromatography over alumina gives 1.487 g of 17β-(1-methoxycyclopentyl) oxy-2α,3α-epithio-5α-androstane. Yield 68.2%. MP 98°C to 101°C.

Therapeutic Function

Antiestrogen

Mepitiostane Preparation Products And Raw materials

Raw materials

Preparation Products

Mepitiostane Suppliers

Global( 13)Suppliers
Supplier Tel Email Country ProdList Advantage
Chemsky (shanghai) International Co.,Ltd 021-50135380 shchemsky@sina.com China 15421 60
Energy Chemical 021-58432009 400-005-6266 marketing@energy-chemical.com China 44941 58
Mepitiostane 10364S 2,3-Epithio-1H-cyclopenta[a]phenanthrene, androstane deriv. 2a,3a-Epithio-17b-(1-methoxycyclopentyloxy)-5a-androstane 2a,3a-Epithio-17b-(cyclopentylmethoxy)-5a-androstane 2a,3a-Epithio-5a-androstan-17b-yl 1-methoxycyclopentyl ether 5a-Androstane, 2a,3a-epithio-17b-[(1-methoxycyclopentyl)oxy]- (8CI) Androstane, 2,3-epithio-17-[(1-methoxycyclopentyl)oxy]-, (2a,3a,5a,17b)- (9CI) Cyclopentanone, 2a,3a-epithio-5a-androstan-17b-yl methyl acetal (8CI) (2α,3α,5α,17β)-2,3-Epithio-17-[(1-Methoxycyclopentyl)oxy]androstane 2α,3α-Epithio-17β-(1-Methoxycyclopentyloxy)-5α-androstane 2α,3α-Epithio-17β-(cyclopentylMethoxy)-5α-androstane 2α,3α-Epithio-5α-androstan-17β-yl 1-Methoxycyclopentyl Ether 2α,3α-Epithio-5α-androstan-17β-yl Methyl Acetal Cyclopentanone Mepitiostane (Contains ~15% 3α,4α-Epithio isomer) Androstane, 2,3-epithio-17-[(1-methoxycyclopentyl)oxy]-, (2α,3α,5α,17β)- 21362-69-6 C25H40O2S Intermediates & Fine Chemicals Pharmaceuticals Steroids