Aristolactam-type alkaloids from orophea enterocarpa and their cytotoxicities

A new aristolactam, named enterocarpam-III (10-amino-2,3,4,6-tetramethoxy phenanthrene-1-carboxylic acid lactam, 1) together with the known alkaloid stigmalactam (2), were isolated from Orophea enterocarpa. Their structures were elucidated on the basis of interpretation of their spectroscopic data....

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Main Authors:	Sanchai Nayyatip, Pak Thaichana, Mongkol Buayairaksa, Wirote Tuntiwechapikul, Puttinan Meepowpan, Narong Nuntasaen, Wilart Pompimon
Format:	Journal
Published:	2018
Subjects:	Biochemistry, Genetics and Molecular Biology Chemical Engineering Chemistry Computer Science
Online Access:	https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84860116503&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/51410
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Institution:	Chiang Mai University

id	th-cmuir.6653943832-51410
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spelling	th-cmuir.6653943832-514102018-09-04T06:03:52Z Aristolactam-type alkaloids from orophea enterocarpa and their cytotoxicities Sanchai Nayyatip Pak Thaichana Mongkol Buayairaksa Wirote Tuntiwechapikul Puttinan Meepowpan Narong Nuntasaen Wilart Pompimon Biochemistry, Genetics and Molecular Biology Chemical Engineering Chemistry Computer Science A new aristolactam, named enterocarpam-III (10-amino-2,3,4,6-tetramethoxy phenanthrene-1-carboxylic acid lactam, 1) together with the known alkaloid stigmalactam (2), were isolated from Orophea enterocarpa. Their structures were elucidated on the basis of interpretation of their spectroscopic data. Compounds 1 and 2 exhibited significant cytotoxicities against human colon adenocarcinoma (HCT15) cell line with IC50 values of 1.68 and 1.32 μM, respectively. © 2012 by the authors. 2018-09-04T06:01:30Z 2018-09-04T06:01:30Z 2012-04-01 Journal 14220067 2-s2.0-84860116503 10.3390/ijms13045010 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84860116503&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/51410
institution	Chiang Mai University
building	Chiang Mai University Library
country	Thailand
collection	CMU Intellectual Repository
topic	Biochemistry, Genetics and Molecular Biology Chemical Engineering Chemistry Computer Science
spellingShingle	Biochemistry, Genetics and Molecular Biology Chemical Engineering Chemistry Computer Science Sanchai Nayyatip Pak Thaichana Mongkol Buayairaksa Wirote Tuntiwechapikul Puttinan Meepowpan Narong Nuntasaen Wilart Pompimon Aristolactam-type alkaloids from orophea enterocarpa and their cytotoxicities
description	A new aristolactam, named enterocarpam-III (10-amino-2,3,4,6-tetramethoxy phenanthrene-1-carboxylic acid lactam, 1) together with the known alkaloid stigmalactam (2), were isolated from Orophea enterocarpa. Their structures were elucidated on the basis of interpretation of their spectroscopic data. Compounds 1 and 2 exhibited significant cytotoxicities against human colon adenocarcinoma (HCT15) cell line with IC50 values of 1.68 and 1.32 μM, respectively. © 2012 by the authors.
format	Journal
author	Sanchai Nayyatip Pak Thaichana Mongkol Buayairaksa Wirote Tuntiwechapikul Puttinan Meepowpan Narong Nuntasaen Wilart Pompimon
author_facet	Sanchai Nayyatip Pak Thaichana Mongkol Buayairaksa Wirote Tuntiwechapikul Puttinan Meepowpan Narong Nuntasaen Wilart Pompimon
author_sort	Sanchai Nayyatip
title	Aristolactam-type alkaloids from orophea enterocarpa and their cytotoxicities
title_short	Aristolactam-type alkaloids from orophea enterocarpa and their cytotoxicities
title_full	Aristolactam-type alkaloids from orophea enterocarpa and their cytotoxicities
title_fullStr	Aristolactam-type alkaloids from orophea enterocarpa and their cytotoxicities
title_full_unstemmed	Aristolactam-type alkaloids from orophea enterocarpa and their cytotoxicities
title_sort	aristolactam-type alkaloids from orophea enterocarpa and their cytotoxicities
publishDate	2018
url	https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84860116503&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/51410
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Aristolactam-type alkaloids from orophea enterocarpa and their cytotoxicities

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