1401938-84-8

Basic information

• Product Name: (3R,5S,5'R,8R,9S,10S,13S,14S)-5'-benzyl-10,13-dimethyltetradecahydro-6'H-spiro[cyclopenta[a]phenanthrene-3,2'-[1,4]oxazinane]-6',17(2H)-dione
• Synonyms: (3R,5S,5'R,8R,9S,10S,13S,14S)-5'-benzyl-10,13-dimethyltetradecahydro-6'H-spiro[cyclopenta[a]phenanthrene-3,2'-[1,4]oxazinane]-6',17(2H)-dione
• CAS NO: 1401938-84-8
• Molecular Weight: 449.634
• Mol File: 1401938-84-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (3R,5S,5'R,8R,9S,10S,13S,14S)-5'-benzyl-10,13-dimethyltetradecahydro-6'H-spiro[cyclopenta[a]phenanthrene-3,2'-[1,4]oxazinane]-6',17(2H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: (3R,5S,5'R,8R,9S,10S,13S,14S)-5'-benzyl-10,13-dimethyltetradecahydro-6'H-spiro[cyclopenta[a]phenanthrene-3,2'-[1,4]oxazinane]-6',17(2H)-dione(1401938-84-8)
• EPA Substance Registry System: (3R,5S,5'R,8R,9S,10S,13S,14S)-5'-benzyl-10,13-dimethyltetradecahydro-6'H-spiro[cyclopenta[a]phenanthrene-3,2'-[1,4]oxazinane]-6',17(2H)-dione(1401938-84-8)

Safety Data

• Hazardous Substances Data: 1401938-84-8(Hazardous Substances Data)

Upstream product

• 15807-55-3 (5S,8R,9S,10S,13S,14S)-10,13-dimethyltetradecahydrospiro[cyclopenta[a]phenanthrene-17,2'-[1,3]dioxolan]-3(2H)-one 
• 84416-35-3 3-hydroxy-5α-androstane-17-one 
• 400604-16-2 spiro-3(R)-oxirane-5α-androstane-17-dioxolane 
• 5717-77-1 (3α,5α)-3-hydroxyandrostan-17-one 1,2-ethanediyl acetal 
• 53-41-8 cis-androsterone 
• 1401938-79-1 (3'R,5'S,5R,8'R,9'S,10'S,13'S,14'S)-5-benzyl-10',13'-dimethyltetradecahydro-2'H,6H-dispiro[1,3-dioxolane-2,17'-cyclopenta[a]phenanthrene-3',2-[1,4]oxazinan]-6-one 
• 1401938-72-4 methyl N-{[(3R,5S,8R,9S,10S,13S,14S)-3-hydroxy-10,13-dimethylhexadecahydrospiro[cyclopenta[a]phenanthrene-17,2'-[1,3]dioxolan]-3-yl]methyl}-D-phenylalaninate 

Relevant articles and documents

Design, chemical synthesis and biological evaluation of 3-spiromorpholinone/3-spirocarbamate androsterone derivatives as inhibitors of 17β-hydroxysteroid dehydrogenase type 3

17β-Hydroxysteroid dehydrogenase type 3 (17β-HSD3) is a key enzyme involved in the biosynthesis of testosterone and dihydrotestosterone. These hormones are known to stimulate androgen-dependent prostate cancer. In order to generate effective inhibitors of androgen biosynthesis without androgenic effect, we synthesized a new family of 3-spiromorpholinone and 3-spirocarbamate androsterone derivatives bearing diversified hydrophobic groups. We also tested their inhibitory activity in a microsomal fraction of 17β-HSD3-containing rat testes, and their androgenic effect on androgen-sensitive LAPC-4 cells. From our first structure-activity relationship (SAR) study, we noted that compound 7e inhibited 17β-HSD3 (77% at 0.1 μM) compared to our reference compound RM-532-105 (76% at 0.1 μM), but exhibited a residual androgenic effect. A library of 7e analogue compounds was next synthesized in order to generate compounds with reduced androgenic activity. In this new SAR study, the sulfonamide compound 7e21 and the carboxamide compound 7e22 inhibited 17β-HSD3 (IC50 = 28 and 88 nM, respectively). These two compounds were not androgenic and not cytotoxic even at the highest concentration tested, but their inhibitory activity decreased in intact LNCaP cells overexpressing 17β-HSD3 (LNCaP[17β-HSD3]). Structural modifications of these two lead compounds could however be tested to produce a second generation of 17β-HSD3 inhibitors.