The structure and biogenesis of desoxyverrucarin E, a metabolite of Eupenicillium hirayamae

R. R. Arndt; C. W. Holzapfel; N. P. Ferreira; J. J. Marsh

doi:10.1016/0031-9422(74)85103-4

The structure and biogenesis of desoxyverrucarin E, a metabolite of Eupenicillium hirayamae

R. R. Arndt
, C. W. Holzapfel
, N. P. Ferreira
, J. J. Marsh

Chemical Sciences

University of Johannesburg
Council for Scientific and Industrial Research

Research output: Contribution to journal › Article › peer-review

3 Citations (Scopus)

Abstract

Desoxyverrucarin E is the main nitrogenous metabolite of Eupenicillium hirayamae. On the basis of chemical and spectroscopic data the compound was identified as 3-acetyl-4-methylpyrrole. Radiochemical data showed that the compound is biogenetically derived from acetate.

Original language	English
Pages (from-to)	1865-1870
Number of pages	6
Journal	Phytochemistry
Volume	13
Issue number	9
DOIs	https://doi.org/10.1016/0031-9422(74)85103-4
Publication status	Published - Sept 1974

Keywords

biogenesis
desoxyverrucarin E.
Eupenicillium hirayamae
pyrrole
structure

ASJC Scopus subject areas

Biochemistry
Molecular Biology
Plant Science
Horticulture

Access to Document

10.1016/0031-9422(74)85103-4

Cite this

@article{c4492c8d681f4564b37c349cd61aecff,

title = "The structure and biogenesis of desoxyverrucarin E, a metabolite of Eupenicillium hirayamae",

abstract = "Desoxyverrucarin E is the main nitrogenous metabolite of Eupenicillium hirayamae. On the basis of chemical and spectroscopic data the compound was identified as 3-acetyl-4-methylpyrrole. Radiochemical data showed that the compound is biogenetically derived from acetate.",

keywords = "biogenesis, desoxyverrucarin E., Eupenicillium hirayamae, pyrrole, structure",

author = "Arndt, \{R. R.\} and Holzapfel, \{C. W.\} and Ferreira, \{N. P.\} and Marsh, \{J. J.\}",

year = "1974",

month = sep,

doi = "10.1016/0031-9422(74)85103-4",

language = "English",

volume = "13",

pages = "1865--1870",

journal = "Phytochemistry",

issn = "0031-9422",

publisher = "Elsevier Ltd.",

number = "9",

}

TY - JOUR

T1 - The structure and biogenesis of desoxyverrucarin E, a metabolite of Eupenicillium hirayamae

AU - Arndt, R. R.

AU - Holzapfel, C. W.

AU - Ferreira, N. P.

AU - Marsh, J. J.

PY - 1974/9

Y1 - 1974/9

N2 - Desoxyverrucarin E is the main nitrogenous metabolite of Eupenicillium hirayamae. On the basis of chemical and spectroscopic data the compound was identified as 3-acetyl-4-methylpyrrole. Radiochemical data showed that the compound is biogenetically derived from acetate.

AB - Desoxyverrucarin E is the main nitrogenous metabolite of Eupenicillium hirayamae. On the basis of chemical and spectroscopic data the compound was identified as 3-acetyl-4-methylpyrrole. Radiochemical data showed that the compound is biogenetically derived from acetate.

KW - biogenesis

KW - desoxyverrucarin E.

KW - Eupenicillium hirayamae

KW - pyrrole

KW - structure

UR - https://www.scopus.com/pages/publications/49549158104

U2 - 10.1016/0031-9422(74)85103-4

DO - 10.1016/0031-9422(74)85103-4

M3 - Article

AN - SCOPUS:49549158104

SN - 0031-9422

VL - 13

SP - 1865

EP - 1870

JO - Phytochemistry

JF - Phytochemistry

IS - 9

ER -

The structure and biogenesis of desoxyverrucarin E, a metabolite of Eupenicillium hirayamae

Abstract

Keywords

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this