20107-90-8 Usage
Uses
Used in Pharmaceutical Research:
(8R,13S)-13-Methyl-17-norkaur-15-en-18-ol is used as a pharmacological agent for its anti-inflammatory and anticancer properties. Its unique structure and stereochemistry contribute to its potential as a therapeutic agent in the treatment of various diseases and conditions.
Used in Drug Development:
In the pharmaceutical industry, (8R,13S)-13-Methyl-17-norkaur-15-en-18-ol is used as a lead compound for the development of new drugs targeting inflammation and cancer. Its biological activities and structural characteristics make it a valuable starting point for designing and synthesizing novel therapeutic agents.
Used in Chemical Synthesis:
(8R,13S)-13-Methyl-17-norkaur-15-en-18-ol can be utilized as a key intermediate in the synthesis of other complex organic compounds, particularly those with potential applications in the pharmaceutical and chemical industries. Its unique stereochemistry and functional groups provide opportunities for further chemical modifications and the creation of new molecules with tailored properties.
Check Digit Verification of cas no
The CAS Registry Mumber 20107-90-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,0 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 20107-90:
(7*2)+(6*0)+(5*1)+(4*0)+(3*7)+(2*9)+(1*0)=58
58 % 10 = 8
So 20107-90-8 is a valid CAS Registry Number.
20107-90-8Relevant academic research and scientific papers
Beyerane derivatives and a sesquiterpene dimer from Japanese Cypress (Chamaecyparis obtusa)
Gao, Hui Yuan,Wu, Li Jun,Muto, Norio,Fuchino, Hiroyuki,Nakane, Takahisa,Shirota, Osamu,Sano, Toshikazu,Kuroyanagi, Masanori
experimental part, p. 1030 - 1034 (2009/08/07)
In the course of studies on biological active constituents from woody plants, we previously reported the isolation of many lignan derivatives as neurite outgrowth-promoting compounds from an ethyl acetate soluble fraction of Japanese Cypress (Chamaecyparis obtusa). Further chemical investigation on the residual parts of the ethyl acetate soluble fraction of a methanol extract of Japanese Cypress resulted in the isolation of four new beyerene type derivatives and a novel sesquiterpene dimer formed between cryptomeridiol and hinokiic acid. Their structures were elucidated as 18-O-(Z)-p-coumaroylbeyer-15-ene-18-ol (1), 18-O-(E)-p-coumaroylbeyer-15-ene-18-ol (2), 18-O-(E)-p-coumaroylbeyer-15- ene-11β,18-diol (3), 18-O-(Z)-p-coumaroylbeyer-15-ene-11β,18-diol (4) and ent-cryptomeridiol-4-yl-hinokiiate (5) by 1H-NMR, 13C-NMR, 2D-NMR, and HR-MS spectral analysis.
