Literature DB >> 6655474

The dermatitis-producing constituents of Euphorbia hermentiana latex.

L J Lin, G T Marshall, A D Kinghorn.   

Abstract

Five ingenane derivatives, 3-O-n-(deca-2,4,6-trienoyl)-16-O-[(Z)-2-methyl-2-butenoyl]-16-hydroxyingenol (1), 3-O-[(Z)-2-methyl-2-butenoyl]-5,16,20-O-triacetyl-16-hydroxyingenol (2), 3-O-[(Z)-2-methyl-2-butenoyl]-16,20-O-diacetyl-16-hydroxyingenol (3), 3-O-[(Z)-2-methyl-2-butenoyl]-20-O-acetylingenol (4), and 3-O-[(Z)-2-methyl-2-butenoyl]-16-O-acetyl-20-deoxy-16-hydroxyingenol (5) were isolated with a new procedure that uses droplet counter-current chromatography, from a dermatitis-producing fraction of the latex of Euphorbia hermentiana Lem. The structures of the new compounds 2,3, and 5 were established by the interpretation of their spectroscopic data and those of their hydrolytic and acetylated derivatives.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6655474     DOI: 10.1021/np50029a020

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


  2 in total

1.  Effects of diterpene esters of tigliane, daphnane, ingenane, and lathyrane types on pink bollworm,Pectinophora gossypiella saunders (Lepidoptera: Gelechiidae).

Authors:  G T Marshall; J A Klocke; L J Lin; A Douglas Kinghorn
Journal:  J Chem Ecol       Date:  1985-02       Impact factor: 2.626

2.  Ingol and Ingenol-Type Diterpenes from Euphorbia trigona Miller with Keratinocyte Inhibitory Activity.

Authors:  Reham Hammadi; Norbert Kúsz; Csilla Zsuzsanna Dávid; Zoltán Behány; László Papp; Lajos Kemény; Judit Hohmann; Lóránt Lakatos; Andrea Vasas
Journal:  Plants (Basel)       Date:  2021-06-14
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.