Literature DB >> 9644058

Macrocyclic diterpenoids from Euphorbia semiperfoliata.

G Appendino1, S Jakupovic, G C Tron, J Jakupovic, V Milon, M Ballero.   

Abstract

In addition to known compounds, the aerial parts of E. semiperfoliata afforded an abietanolide (3), 13 jatrophane polyesters (4-9, 12, 14-19), two 4-deoxyphorbol diesters (23, 24), and a pair of epimeric diterpenes (21, 22) with a novel carbon skeleton, which was named euphoperfoliane. Structures were determined by spectroscopic analysis, and the main conformational features of jatropha-6(17),11-dienes are discussed in detail. The obtained isolation yield of several jatrophanes was unprecedented within the spurges (Euphorbia spp.), making E. semiperfoliata a unique source of macrocyclic diterpenoids.

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Year:  1998        PMID: 9644058     DOI: 10.1021/np970507w

Source DB:  PubMed          Journal:  J Nat Prod        ISSN: 0163-3864            Impact factor:   4.050


  5 in total

1.  New mirsinane-type diterpenes from Euphorbia microsciadia Boiss. with inhibitory effect on VEGF-induced angiogenesis.

Authors:  Syed Mustafa Ghanadian; Abdul Majid Ayatollahi; Suleiman Afsharypuor; Shaghayegh Haghjooy Javanmard; Nasim Dana
Journal:  J Nat Med       Date:  2012-07-15       Impact factor: 2.343

2.  New tigliane-type diterpenoids from Euphorbia aellenii Rech. f. with immunomodulatory activity.

Authors:  M Ghanadian; A M Ayatollahi; M A Mesaik; S Afsharypuor; O M Abdalla; F Kobarfard
Journal:  Res Pharm Sci       Date:  2011-01

Review 3.  Jatrophane and rearranged jatrophane-type diterpenes: biogenesis, structure, isolation, biological activity and SARs (1984-2019).

Authors:  Maryam Fattahian; Mustafa Ghanadian; Zulfiqar Ali; Ikhlas A Khan
Journal:  Phytochem Rev       Date:  2020-04-13       Impact factor: 7.741

4.  13C-NMR data of three important diterpenes isolated from Euphorbia species.

Authors:  Qi-Cheng Wu; Yu-Ping Tang; An-Wei Ding; Fen-Qiang You; Li Zhang; Jin-Ao Duan
Journal:  Molecules       Date:  2009-11-06       Impact factor: 4.411

5.  Euphormins A and B, New Pyranocoumarin Derivatives from Euphorbia formosana Hayata, and Their Anti-Inflammatory Activity.

Authors:  Yu-Hsuan Lan; I-Hsiao Chen; Hsin-Hung Lu; Ting-Jing Guo; Tsong-Long Hwang; Yann-Lii Leu
Journal:  Molecules       Date:  2022-03-14       Impact factor: 4.411

  5 in total

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