83117-10-6 Usage
General Description
The chemical (1beta,12alpha,15beta)-15-heptyl-1,11,12-trihydroxy-11,20-epoxypicras-3-ene-2,16-dione is a complex organic compound that contains a heptyl chain, multiple hydroxyl groups, and an epoxide ring. It belongs to the class of picrasane-type diterpenoids, which are naturally occurring compounds found in certain plants. These types of compounds have been studied for their potential biological activities, including anti-inflammatory, antimicrobial, and antitumor properties. The specific chemical structure of (1beta,12alpha,15beta)-15-heptyl-1,11,12-trihydroxy-11,20-epoxypicras-3-ene-2,16-dione suggests that it may have similar pharmacological activities and could be of interest for further research and development in the pharmaceutical and medical fields.
Check Digit Verification of cas no
The CAS Registry Mumber 83117-10-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,1,1 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 83117-10:
(7*8)+(6*3)+(5*1)+(4*1)+(3*7)+(2*1)+(1*0)=106
106 % 10 = 6
So 83117-10-6 is a valid CAS Registry Number.
83117-10-6Relevant articles and documents
Biologically active quassinoids : synthetic methodology for the conversion of chaparrin into glaucarubolone esters and quassinoid analogs1 1 For previous paper in this series see: C. Moretti, S. Bhatnagar, J.C. Beloeil and J. Polonsky, J. Nat. Prods., 49, 440 (1986)
Bhatnagar, Subodh C.,Caruso, Andrew J.,Polonsky, Judith,Rodriguez, Berta Soto
, p. 3471 - 3480 (2007/10/02)
Biologically inactive but easily available chaparrin 2a has been converted into potent antileukemic C-15 esters of glaucarubolone 2b and quassinoid analogs in which the C-15 ester side chain has been replaced by an alkyl or alkenyl group.The synthetic methodology developed has been applied to the preparation of C-15 ester derivatives 15, 16, 17 and quassinoid analogs 12, 13 and 14.
