66979-63-3 Usage
Uses
Used in Pharmaceutical Research:
(3S,8S,9S,10R,13S,14S,17S)-10,13-dimethyl-17-[(2E)-3-phenylprop-2-enoyl]-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl acetate (non-preferred name) is used as a potential pharmaceutical candidate for exploring its biological activities and pharmacological properties. Its unique structure and functional groups may contribute to the development of new drugs or therapeutic agents.
Used in Chemical Research:
In the field of chemical research, (3S,8S,9S,10R,13S,14S,17S)-10,13-dimethyl-17-[(2E)-3-phenylprop-2-enoyl]-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl acetate (non-preferred name) serves as a subject for studying its chemical properties, reactivity, and potential applications in the synthesis of other complex organic compounds.
Used in Biological Research:
(3S,8S,9S,10R,13S,14S,17S)-10,13-dimethyl-17-[(2E)-3-phenylprop-2-enoyl]-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl acetate (non-preferred name) is utilized in biological research to investigate its interactions with biological systems, such as its potential effects on cellular processes, signaling pathways, or its ability to target specific proteins or enzymes. This research may lead to a better understanding of its therapeutic potential and mechanisms of action.
Check Digit Verification of cas no
The CAS Registry Mumber 66979-63-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,9,7 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 66979-63:
(7*6)+(6*6)+(5*9)+(4*7)+(3*9)+(2*6)+(1*3)=193
193 % 10 = 3
So 66979-63-3 is a valid CAS Registry Number.
66979-63-3Relevant academic research and scientific papers
Rapid microwave assisted synthesis and antimicrobial bioevaluation of novel steroidal chalcones
Kakati, Dwipen,Sarma, Rupak K.,Saikia, Ratul,Barua, Nabin C.,Sarma, Jadab C.
, p. 321 - 326 (2013/03/28)
A novel class of chalconoyl pregnenolones has been prepared via Claisen-Schmidt condensation under microwave activation and solvent free reaction conditions. The compounds were screened for antimicrobial activity against two bacterial strains Bacillus subtilis and Escherichia coli and two fungal strains Aspergillus niger and Candida albicans. Some of the compounds exhibited significant inhibitory activity against the microbial strains. Presence of the α,β-unsaturated carbonyl moiety in the synthesized compounds was found to be essential for the activity as manipulation of the same through epoxidation of the double bond diminished the activity.
