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4-epi-vulgarin is a naturally occurring sesquiterpene lactone compound, characterized by its unique chemical structure and biological properties. It is found in various plant species, particularly in the genus Artemisia, which includes mugwort and wormwood. 4-epi-vulgarin exhibits a wide range of pharmacological activities, such as anti-inflammatory, antimicrobial, and anticancer effects. The chemical structure of 4-epi-vulgarin consists of a tricyclic sesquiterpene lactone with a 4-epi configuration, which differentiates it from other related compounds like vulgarin. Due to its potential therapeutic applications, 4-epi-vulgarin has been the subject of extensive research, with ongoing studies aimed at understanding its mechanisms of action and exploring its potential as a novel therapeutic agent.

2615-39-6

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2615-39-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2615-39-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,1 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2615-39:
(6*2)+(5*6)+(4*1)+(3*5)+(2*3)+(1*9)=76
76 % 10 = 6
So 2615-39-6 is a valid CAS Registry Number.

2615-39-6Downstream Products

2615-39-6Relevant academic research and scientific papers

Microbial Transformations of Sesquiterpenoids: Conversion of Deoxyvulgarin by Rhizopus nigricans and Aspargillus ochraceous

Arias, Jose M.,Breton, Jose L.,Gavin, Jose A.,Garcia-Granados, Andres,Martinez, Antonio,Onorato, M. Esther

, p. 471 - 474 (2007/10/02)

Microbial transformation of the sesquiterpene lactone deoxyvulgarin (2) has been carried out with Aspergillus ochraceous and Rhizopus nigricans cultures.A. ochraceous converted deoxyvulgarin (2) into vulgarin (3) and 11,13-dihydrodouglanin (4).R. nigricans transformed deoxyvulgarin (2) into vulgarin (3), erivanin (6), and 1β-hydroxy-2-oxoeudesm-3-en-6,13-olide (7).Vulgarin (3) was obtained chemically by epoxidation of deoxyvulgarin (2) in one-step process in virtually quantitative yield.A pathway proposed for the conversion of deoxyvulgarin (2) into more functionalized metabolites is discussed.

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