115473-63-7 Usage
General Description
Rupestonic acid is a sesquiterpene lactone compound found in the plant Artemisia rupestris. It has been identified as a potential bioactive compound with various pharmacological properties, including anti-inflammatory, anti-tumor, and antimicrobial activities. Studies have shown that rupestonic acid exhibits anti-inflammatory effects by inhibiting the production of pro-inflammatory cytokines and enzymes. Additionally, it has demonstrated anti-tumor activity by inducing apoptosis and inhibiting cancer cell proliferation. Its antimicrobial properties have been attributed to its ability to disrupt bacterial cell membranes and inhibit the growth of certain pathogens. Overall, rupestonic acid is considered to be a promising natural compound with potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 115473-63-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,4,7 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 115473-63:
(8*1)+(7*1)+(6*5)+(5*4)+(4*7)+(3*3)+(2*6)+(1*3)=117
117 % 10 = 7
So 115473-63-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H20O3/c1-8-4-5-11(9(2)15(17)18)6-13-10(3)14(16)7-12(8)13/h8,11-12H,2,4-7H2,1,3H3,(H,17,18)/t8-,11-,12-/m0/s1
115473-63-7Relevant articles and documents
Asymmetric Synthesis of Rupestonic Acid and Pechueloic Acid
Han, Pan,Zhou, Zhu,Si, Chang-Mei,Sha, Xian-Yi,Gu, Zheng-Yi,Wei, Bang-Guo,Lin, Guo-Qiang
, p. 6732 - 6735 (2017)
In this report, the originally proposed rupestonic acid (5) and pechueloic acid (3) were efficiently synthesized. The chiral lactone 13, recycled from the degradation of saponin glycosides, was utilized to prepare the key chiral fragment 11. During the exploration of this convergent assembly strategy, the ring-closing metathesis (RCM), SmI2-prompted intermolecular addition, and [2,3]-Wittig rearrangement proved to be effective transformations for the synthesis of subunits.