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CAS 2034-94-8

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(17β)-17-(3-Cyclohexyl-1-oxopropoxy)androst-4-en-3-one

Description:
The chemical substance known as "(17β)-17-(3-Cyclohexyl-1-oxopropoxy)androst-4-en-3-one," with the CAS number 2034-94-8, is a synthetic steroid derivative. It features a steroid backbone, specifically the androstane structure, which is characterized by a four-ring core structure typical of steroids. The presence of a cyclohexyl group and an oxopropoxy substituent at the 17β position contributes to its unique chemical properties and potential biological activity. This compound may exhibit interactions with steroid receptors, influencing various physiological processes. Its structural modifications can affect its solubility, stability, and bioavailability, making it of interest in pharmaceutical research, particularly in the development of anabolic agents or hormone therapies. Additionally, the compound's potential applications may extend to areas such as endocrinology and oncology, where steroidal compounds are often explored for therapeutic benefits. However, detailed studies on its pharmacodynamics, pharmacokinetics, and safety profile would be necessary to fully understand its characteristics and potential uses.
Formula:C28H42O3
InChI:InChI=1S/C28H42O3/c1-27-16-14-21(29)18-20(27)9-10-22-23-11-12-25(28(23,2)17-15-24(22)27)31-26(30)13-8-19-6-4-3-5-7-19/h18-19,22-25H,3-17H2,1-2H3/t22-,23-,24-,25-,27-,28-/m0/s1
InChI key:InChIKey=HFFZTSFKTLANED-FEZCWRLCSA-N
SMILES:C[C@@]12[C@@]3([C@]([C@]4([C@](C)(CC3)[C@@H](OC(CCC5CCCCC5)=O)CC4)[H])(CCC1=CC(=O)CC2)[H])[H]
Synonyms:
  • (17beta)-3-oxoandrost-4-en-17-yl 3-cyclohexylpropanoate
  • Testosterone cyclohexanepropionate
  • Androst-4-en-3-one, 17-(3-cyclohexyl-1-oxopropoxy)-, (17β)-
  • (17β)-17-(3-Cyclohexyl-1-oxopropoxy)androst-4-en-3-one
  • Testosterone 3-cyclohexylpropionate
  • Testosterone, cyclohexanepropionate
  • Testosterone cyclohexylpropionate
  • Einecs 217-998-0
  • Cyclohexanepropionic acid 3-oxoandrost-4-en-17β-yl ester
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