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Arteannuin M, a sesquiterpene lactone found in the sweet wormwood plant (Artemisia annua), is recognized for its anti-inflammatory, antimalarial, and anticancer properties. Its unique structure and biological activities position it as a promising candidate for therapeutic applications in various medical fields.

207446-90-0

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207446-90-0 Usage

Uses

Used in Pharmaceutical Industry:
Arteannuin M is used as an anticancer agent for its cytotoxic and antiproliferative effects on cancer cells, making it a potential novel treatment for various types of cancer.
Used in Antimalarial Applications:
Arteannuin M is used as an antimalarial agent due to its ability to inhibit the growth of the Plasmodium falciparum parasite, which causes malaria. This property highlights its potential in the development of new antimalarial drugs.
Further research is necessary to fully explore the therapeutic potential of Arteannuin M, but its diverse biological activities and promising preliminary findings make it an intriguing compound for future development in the medical and pharmaceutical sectors.

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.

207446-90-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (3R,3aS,6R,6aS,9R,10R,10aS)-9,10-Dihydroxy-3,6,9-trimethyldecahyd ro-2H-naphtho[8a,1-b]furan-2-one

1.2 Other means of identification

Product number -
Other names arteanniun M

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:207446-90-0 SDS

207446-90-0Downstream Products

207446-90-0Relevant academic research and scientific papers

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.

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