207446-90-0 Usage
General Description
Arteannuin M is a chemical compound found in the sweet wormwood plant, Artemisia annua. It belongs to a class of compounds known as sesquiterpene lactones, which are known for their anti-inflammatory, antimalarial, and anticancer properties. Arteannuin M has been studied for its potential as a novel anticancer agent, as it possesses cytotoxic and antiproliferative effects on cancer cells. Additionally, it has shown promise as an antimalarial agent, with research demonstrating its ability to inhibit the growth of the malaria-causing parasite Plasmodium falciparum. Further studies are needed to fully understand the potential therapeutic applications of Arteannuin M, but its diverse biological activities make it an intriguing compound for further research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 207446-90-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,4,4 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 207446-90:
(8*2)+(7*0)+(6*7)+(5*4)+(4*4)+(3*6)+(2*9)+(1*0)=130
130 % 10 = 0
So 207446-90-0 is a valid CAS Registry Number.
207446-90-0Relevant articles and documents
Structure elucidation of arteannuin O, a novel cadinane diol from Artemisia annua, and the synthesis of arteannuins K, L, M and O
Sy, Lai-King,Cheung, Kung-Kai,Zhu, Nian-Yong,Brown, Geoffrey D
, p. 8481 - 8493 (2007/10/03)
The novel cadinane diol, arteannuin O (1), has been obtained from Artemisia annua and its structure has been established by 2D NMR and X-ray crystallography. A reconstructive synthesis of arteannuin O from artemisinin is described, which also yields the natural products arteannuin K and arteannuin L. Mechanistic considerations have led to the conclusion that the stereochemistry of the 5-hydroxyl group was wrongly assigned when arteannuins K, L and M were first reported as natural products. This was confirmed by derivatization of synthetic arteannuins K, L and M as their Mosher esters.