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CAS 19595-18-7

:

(2beta,3beta,5beta,22R,25S)-2,3,14,20,22,26-hexahydroxycholest-7-en-6-one

Description:
The chemical substance known as "(2beta,3beta,5beta,22R,25S)-2,3,14,20,22,26-hexahydroxycholest-7-en-6-one," with the CAS number 19595-18-7, is a steroid derivative characterized by a complex polycyclic structure typical of cholesterol and its analogs. This compound features multiple hydroxyl (-OH) groups, which contribute to its hydrophilicity and influence its biological activity. The specific stereochemistry indicated by the beta and R/S designations suggests a particular three-dimensional arrangement of atoms, which is crucial for its interaction with biological systems. The presence of a ketone functional group at the 6-position further modifies its reactivity and potential applications. Such compounds are often studied for their roles in biological processes, including cell membrane structure and signaling pathways. Additionally, the presence of multiple hydroxyl groups may enhance solubility in polar solvents, making it of interest in pharmaceutical and biochemical research. Overall, this compound exemplifies the structural diversity and functional complexity found within steroid chemistry.
Formula:C27H44O7
InChI:InChI=1/C27H44O7/c1-15(14-28)5-6-23(32)26(4,33)22-8-10-27(34)17-11-19(29)18-12-20(30)21(31)13-24(18,2)16(17)7-9-25(22,27)3/h11,15-16,18,20-23,28,30-34H,5-10,12-14H2,1-4H3/t15-,16-,18-,20+,21-,22-,23+,24+,25+,26+,27+/m0/s1
Synonyms:
  • cholest-7-en-6-one, 2,3,14,20,22,26-hexahydroxy-, (2beta,3beta,5beta,22R,25S)-
  • (2beta,3beta,5beta,22R,25S)-2,3,14,20,22,26-Hexahydroxycholest-7-en-6-one
  • 25S-Inokosterone
  • Cholest-7-en-6-one, 2,3,14,20,22,26-hexahydroxy-, (2β,3β,5β,22R,25S)-
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