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CAS 76763-14-9

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17β-Carboxy-5-oxo-A-nor-3,5-secoandrostan-3-oic acid

Description:
17β-Carboxy-5-oxo-A-nor-3,5-secoandrostan-3-oic acid, with the CAS number 76763-14-9, is a synthetic steroid derivative that belongs to the class of androgens and anabolic steroids. This compound features a unique structural modification, characterized by the presence of a carboxylic acid group and a ketone functional group, which contribute to its chemical reactivity and potential biological activity. The "A-nor" designation indicates the absence of a carbon atom at a specific position in the steroid framework, which can influence its interaction with biological targets. This compound may exhibit properties relevant to hormonal activity, making it of interest in pharmacological research, particularly in the context of steroid metabolism and potential therapeutic applications. Its solubility, stability, and reactivity can vary based on environmental conditions and the presence of other chemical species. As with many steroid derivatives, understanding its pharmacokinetics and biological effects requires further investigation through empirical studies.
Formula:C19H28O5
InChI:InChI=1S/C19H28O5/c1-18-9-7-13-11(12(18)4-5-14(18)17(23)24)3-6-15(20)19(13,2)10-8-16(21)22/h11-14H,3-10H2,1-2H3,(H,21,22)(H,23,24)/t11-,12-,13-,14+,18-,19+/m0/s1
InChI key:InChIKey=SXMYTVFDBSFKNU-UUBMZHIOSA-N
SMILES:C[C@@]12[C@]([C@]3([C@@]([C@](CCC(O)=O)(C)C(=O)CC3)(CC1)[H])[H])(CC[C@@H]2C(O)=O)[H]
Synonyms:
  • (3S,3aS,5aS,6R,9aS,9bS)-3-Carboxydodecahydro-3a,6-dimethyl-7-oxo-1H-benz[e]indene-6-propanoic acid
  • 1H-Benz[e]indene-6-propanoic acid, 3-carboxydodecahydro-3a,6-dimethyl-7-oxo-, (3S,3aS,5aS,6R,9aS,9bS)-
  • 17β-Carboxy-5-oxo-A-nor-3,5-secoandrostan-3-oic acid
  • 1H-Benz[e]indene-6-propanoic acid, 3-carboxydodecahydro-3a,6-dimethyl-7-oxo-, [3S-(3α,3aα,5aβ,6β,9aα,9bβ)]-
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