1102-96-1 Usage
Steroid molecule
Derived from pregnane
A naturally occurring steroid hormone that serves as the base structure for this compound.
Acetyloxy group
Present at the 12α position
A functional group consisting of an acetyl (C2H3O2) moiety attached to the steroid ring.
Hydroxy group
Located at the 3α position
A functional group consisting of an oxygen atom bonded to a hydrogen atom, attached to the steroid ring.
Biological processes
Involved in various pathways
The compound is believed to play a role in hormonal and metabolic regulation.
Pharmacological activity
Potential for exhibiting activity
The structural features of the compound may contribute to its ability to interact with biological targets.
Documentation
Limited information available
The precise functions and activities of this compound in the body are not well documented.
Further research
Necessary for elucidation
The specific role and significance of this compound in biological systems require additional investigation.
Check Digit Verification of cas no
The CAS Registry Mumber 1102-96-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,0 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1102-96:
(6*1)+(5*1)+(4*0)+(3*2)+(2*9)+(1*6)=41
41 % 10 = 1
So 1102-96-1 is a valid CAS Registry Number.
1102-96-1Relevant articles and documents
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Reichstein,v. Arx
, p. 747,749 (1940)
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Synthesis of Hoodigogenin A, aglycone of natural appetite suppressant glycosteroids extracted from Hoodia gordonii
Geoffroy, Philippe,Ressault, Blandine,Marchioni, Eric,Miesch, Michel
, p. 702 - 708 (2011)
14β-hydroxy pregnane glycosides extracted from Hoodia gordonii, a succulent plant isolated from Apocynaceae are suggested to have appetite suppressant properties in animals and humans. However, limited reports on biological studies concerning the appetite suppressant properties are available in the open literature. One reason for that is the poor availability of these glycosteroids because H. gordonii is a protected plant and the yield of extraction lies between 0.003% and 0.02%. Starting from 3α,12α- diacetoxy-pregnanone 1, we disclose in this report the synthesis of Hoodigogenin A, the aglycone of the natural 14β-hydroxy pregnane glycosides extracted from H. Gordonii.
