Reduced Perylenequinone Derivatives from an Endophytic Alternaria sp. Isolated from Pinus ponderosa
Document Type
Article
Publication Date
3-2015
Publication Source
Phytochemistry Letters
Abstract
The consecutive solvent extraction of endophytic Alternaria sp. (DC401) isolated from Pinus ponderosa followed by chromatographic techniques led to the isolation of five perylenequinone compounds and one dihydronaphthaquinone derivative, which include three new perylenequinones (1–3). The compounds were identified as 6-methoxy-3,6a,7,10-tetrahydroxy-4,9-dioxo-4,5,6,6a,6b,7,8,9-octahydroperylene (1), 3,6a,9,10-tetrahydroxy-7,8-epoxy-4-oxo-4,5,6,6a,6b,7,8,9-octahydroperylene (2), 6-methoxy-3,6a,9,10-tetrahydroxy-7,8-epoxy-4-oxo-4,5,6,6a,6b,7,8,9-octahydroperylene (3), 3,6a,7,10-tetrahydroxy-4,9-dioxo-4,5,6,6a,6b,7,8,9-octahydroperylene (altertoxin I) (4), 3,6a,7,10-tetrahydroxy-4,9-dioxo-4,6a,6b,7,8,9-hexahydroperylene (dehydroaltertoxin I) (5), and 7-chloroscytalone (6). Structure of compounds 1–6 was determined on the basis of detailed spectroscopic analysis, as well as by comparison with literature reports. The antileismanial, antimicrobial, antimalarial and in vitro cytotoxic activities of compounds 1–6 were evaluated.
Inclusive pages
264–269
ISBN/ISSN
1874-3900
Copyright
Copyright © 2015, Phytochemical Society of Europe
Publisher
Elsevier
Volume
11
Peer Reviewed
yes
eCommons Citation
Idris, Ahmed; Tantry, Mudasir A.; Ganai, Bashir A.; Kamili, Azra N.; and Williamson, John S., "Reduced Perylenequinone Derivatives from an Endophytic Alternaria sp. Isolated from Pinus ponderosa" (2015). Office for Research Publications and Presentations. 12.
https://ecommons.udayton.edu/ofr_pub/12
Comments
Permission documentation is on file.