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Picture of Mixure of 6α & 6β Hydroxyperoxy Testosterone

Mixure of 6α & 6β Hydroxyperoxy Testosterone

SZ CAT No:SZ-T021074
CAS NoNA
Mol.F.C19H28O5
Mol.Wt.320.4
Inv. StatusCustom Synthesis

Chemical Name: (6R,8R,9S,10R,13S,14S,17S)-6-Hydroperoxy-17-hydroxy-10,13-dimethyl-1,2,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-3H-cyclopenta[a]phenanthren-3-one compound with (6S,8R,9S,10R,13S,14S,17S)-6-hydroperoxy-17-hydroxy-10,13-dimethyl-1,2,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-3H-cyclopenta[a]phenanthren-3-one (1:1)

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Smiles: O=C1CC[C@]2(C)[C@@]3([H])CC[C@]4(C)[C@@H](O)CC[C@@]4([H])[C@]3([H])C[C@H](OO)C2=C1.C[C@@](C([C@H](OO)C5)=CC6=O)(CC6)[C@]7([H])[C@]5([H])[C@@](CC[C@@H]8O)([H])[C@]8(C)CC7

Complete NMR assignment and absolute configuration of k4610422, a norditerpenoid inhibitor of testosterone-​5α-​reductase originally from Streptosporangium: rediscovery from a thermophilic Actinomadura
By Akiyama, Hirofumi; Oku, Naoya; Harunari, Enjuro; Panbangred, Watanalai; Igarashi, Yasuhiro
From Journal of Antibiotics (2020), 73(1), 60-65
 
Spectrophotometric and chromatographic strategies for exploring of the nanostructure pharmaceutical formulations which contains testosterone undecanoate
By Butnariu, Monica; Sarac, Ioan; Samfira, Ionel
From Scientific Reports (2020), Ahead of Print.
 

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