Oblongolides from the endophytic fungus Phomopsis sp. BCC 9789

Six new oblongolides, W1, W2, X, Y, and Z (1-3, 6, 7) and 2-deoxy-4α-hydroxyoblongolide X (4), and the known compounds oblongolide (8), oblongolides T, C, and Q (5, 9, 10), and (-)-5-methylmellein were isolated from the endophytic fungus Phomopsis sp. BCC 9789. Compound 7 showed anti-HSV-1 activity...

Full description

Saved in:
Bibliographic Details
Main Authors: Bunyapaiboonsri T., Yoiprommarat S., Srikitikulchai P., Srichomthong K., Lumyong S.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-76049090657&partnerID=40&md5=ac22e188ad5b5d0ffbca76c7d743651e
http://cmuir.cmu.ac.th/handle/6653943832/6363
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Chiang Mai University
Language: English
id th-cmuir.6653943832-6363
record_format dspace
spelling th-cmuir.6653943832-63632014-08-30T03:24:08Z Oblongolides from the endophytic fungus Phomopsis sp. BCC 9789 Bunyapaiboonsri T. Yoiprommarat S. Srikitikulchai P. Srichomthong K. Lumyong S. Six new oblongolides, W1, W2, X, Y, and Z (1-3, 6, 7) and 2-deoxy-4α-hydroxyoblongolide X (4), and the known compounds oblongolide (8), oblongolides T, C, and Q (5, 9, 10), and (-)-5-methylmellein were isolated from the endophytic fungus Phomopsis sp. BCC 9789. Compound 7 showed anti-HSV-1 activity (IC50 ) 14 μM) and cytotoxic activities against KB, BC, NCI-H187, and nonmalignant (Vero) cell lines with respective IC50 values of 37, 26, 32, and 60 μM. Cytotoxic activity against the BC cell line was also observed for compound 6, with an IC50 value of 48 μM. © 2010 American Chemical Society and American Society of Pharmacognosy. 2014-08-30T03:24:08Z 2014-08-30T03:24:08Z 2010 Article 1633864 10.1021/np900650c 20038128 JNPRD http://www.scopus.com/inward/record.url?eid=2-s2.0-76049090657&partnerID=40&md5=ac22e188ad5b5d0ffbca76c7d743651e http://cmuir.cmu.ac.th/handle/6653943832/6363 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description Six new oblongolides, W1, W2, X, Y, and Z (1-3, 6, 7) and 2-deoxy-4α-hydroxyoblongolide X (4), and the known compounds oblongolide (8), oblongolides T, C, and Q (5, 9, 10), and (-)-5-methylmellein were isolated from the endophytic fungus Phomopsis sp. BCC 9789. Compound 7 showed anti-HSV-1 activity (IC50 ) 14 μM) and cytotoxic activities against KB, BC, NCI-H187, and nonmalignant (Vero) cell lines with respective IC50 values of 37, 26, 32, and 60 μM. Cytotoxic activity against the BC cell line was also observed for compound 6, with an IC50 value of 48 μM. © 2010 American Chemical Society and American Society of Pharmacognosy.
format Article
author Bunyapaiboonsri T.
Yoiprommarat S.
Srikitikulchai P.
Srichomthong K.
Lumyong S.
spellingShingle Bunyapaiboonsri T.
Yoiprommarat S.
Srikitikulchai P.
Srichomthong K.
Lumyong S.
Oblongolides from the endophytic fungus Phomopsis sp. BCC 9789
author_facet Bunyapaiboonsri T.
Yoiprommarat S.
Srikitikulchai P.
Srichomthong K.
Lumyong S.
author_sort Bunyapaiboonsri T.
title Oblongolides from the endophytic fungus Phomopsis sp. BCC 9789
title_short Oblongolides from the endophytic fungus Phomopsis sp. BCC 9789
title_full Oblongolides from the endophytic fungus Phomopsis sp. BCC 9789
title_fullStr Oblongolides from the endophytic fungus Phomopsis sp. BCC 9789
title_full_unstemmed Oblongolides from the endophytic fungus Phomopsis sp. BCC 9789
title_sort oblongolides from the endophytic fungus phomopsis sp. bcc 9789
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-76049090657&partnerID=40&md5=ac22e188ad5b5d0ffbca76c7d743651e
http://cmuir.cmu.ac.th/handle/6653943832/6363
_version_ 1681420599854891008