1173-30-4 Usage
Chemical structure
Steroidal compound with a methyl ester group attached to the carboxylic acid moiety.
Bile acid derivative
Derived from lithocholic acid, a naturally occurring bile acid.
Function in digestion
Involved in the emulsification of fats and absorption of lipids in the small intestine.
Signaling molecule
Regulates various physiological processes, including lipid metabolism, glucose homeostasis, and inflammation.
Therapeutic applications
Studied for potential use in treating metabolic disorders, liver diseases, and gastrointestinal conditions.
Cancer research
Investigated for its role in cancer prevention and treatment.
Biological functions
Plays a crucial role in various biological functions and has potential implications for human health.
These properties and specific content provide a comprehensive overview of the characteristics and potential applications of 12-Oxo-5β-cholan-24-oic acid methyl ester.
Check Digit Verification of cas no
The CAS Registry Mumber 1173-30-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,7 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1173-30:
(6*1)+(5*1)+(4*7)+(3*3)+(2*3)+(1*0)=54
54 % 10 = 4
So 1173-30-4 is a valid CAS Registry Number.
1173-30-4Relevant academic research and scientific papers
Improved enantioselectivity in the epoxidation of cinnamic acid derivatives with dioxiranes from keto bile acids
Bortolini, Olga,Fantin, Giancarlo,Fogagnolo, Marco,Forlani, Roberto,Maietti, Silvia,Pedrini, Paola
, p. 5802 - 5806 (2007/10/03)
The asymmetric epoxidation of substituted cinnamic acids has been obtained in the presence of different keto bile acid derivatives as optically active carbonyl inducers and Oxone as oxygen source. Predominant or almost exclusive formation of both enantiomeric epoxides is obtained (ee up to 95%) depending on the specific substitution at carbons C(7) and C(12) of the bile acid.
Autooxidation of Cholanic Acid in the Presence of Ferrous Ions
Sawaya, Takuji,Kimura, Michiya
, p. 1207 - 1212 (2007/10/02)
Autooxidation of cholanic acid in an aqueous acetone solution containing 0.2 M acetate buffer (pH 5.0) and ferrous sulfate gave three C(12)-keto products, A, B, and C.The main product A was elucidated to be 12-oxo-5β-cholan-24-oic acid.The minor product B