Rearranged benzophenones and prenylated xanthones from Garcinia propinqua twigs

The first phytochemical investigation of Garcinia propinqua has led to the isolation and identification of three new compounds, including two rearranged benzophenones, doitunggarcinones A (1) and B (2), and a xanthone, doitunggarcinone C (3), together with seven known compounds (4-10). The structure...

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Main Authors: Cholpisut Tantapakul, Wong Phakhodee, Thunwadee Ritthiwigrom, Sarot Cheenpracha, Uma Prawat, Suwanna Deachathai, Surat Laphookhieo
Format: Journal
Published: 2018
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/51355
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spelling th-cmuir.6653943832-513552018-09-04T06:13:13Z Rearranged benzophenones and prenylated xanthones from Garcinia propinqua twigs Cholpisut Tantapakul Wong Phakhodee Thunwadee Ritthiwigrom Sarot Cheenpracha Uma Prawat Suwanna Deachathai Surat Laphookhieo Biochemistry, Genetics and Molecular Biology Chemistry Medicine Pharmacology, Toxicology and Pharmaceutics The first phytochemical investigation of Garcinia propinqua has led to the isolation and identification of three new compounds, including two rearranged benzophenones, doitunggarcinones A (1) and B (2), and a xanthone, doitunggarcinone C (3), together with seven known compounds (4-10). The structures of 1-3 were elucidated on the basis of spectroscopic methods, including UV, IR, NMR, and MS. The antibacterial activity of the 10 isolates was evaluated against Escherichia coli TISTR 780, Salmonella typhimurium TISTR 292, Staphylococcus aureus TISTR 1466, and methicillin-resistant Staphylococcus aureus (MRSA) SK1. © 2012 The American Chemical Society and American Society of Pharmacognosy. 2018-09-04T06:00:41Z 2018-09-04T06:00:41Z 2012-09-28 Journal 15206025 01633864 2-s2.0-84867002348 10.1021/np300487w https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84867002348&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/51355
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Biochemistry, Genetics and Molecular Biology
Chemistry
Medicine
Pharmacology, Toxicology and Pharmaceutics
spellingShingle Biochemistry, Genetics and Molecular Biology
Chemistry
Medicine
Pharmacology, Toxicology and Pharmaceutics
Cholpisut Tantapakul
Wong Phakhodee
Thunwadee Ritthiwigrom
Sarot Cheenpracha
Uma Prawat
Suwanna Deachathai
Surat Laphookhieo
Rearranged benzophenones and prenylated xanthones from Garcinia propinqua twigs
description The first phytochemical investigation of Garcinia propinqua has led to the isolation and identification of three new compounds, including two rearranged benzophenones, doitunggarcinones A (1) and B (2), and a xanthone, doitunggarcinone C (3), together with seven known compounds (4-10). The structures of 1-3 were elucidated on the basis of spectroscopic methods, including UV, IR, NMR, and MS. The antibacterial activity of the 10 isolates was evaluated against Escherichia coli TISTR 780, Salmonella typhimurium TISTR 292, Staphylococcus aureus TISTR 1466, and methicillin-resistant Staphylococcus aureus (MRSA) SK1. © 2012 The American Chemical Society and American Society of Pharmacognosy.
format Journal
author Cholpisut Tantapakul
Wong Phakhodee
Thunwadee Ritthiwigrom
Sarot Cheenpracha
Uma Prawat
Suwanna Deachathai
Surat Laphookhieo
author_facet Cholpisut Tantapakul
Wong Phakhodee
Thunwadee Ritthiwigrom
Sarot Cheenpracha
Uma Prawat
Suwanna Deachathai
Surat Laphookhieo
author_sort Cholpisut Tantapakul
title Rearranged benzophenones and prenylated xanthones from Garcinia propinqua twigs
title_short Rearranged benzophenones and prenylated xanthones from Garcinia propinqua twigs
title_full Rearranged benzophenones and prenylated xanthones from Garcinia propinqua twigs
title_fullStr Rearranged benzophenones and prenylated xanthones from Garcinia propinqua twigs
title_full_unstemmed Rearranged benzophenones and prenylated xanthones from Garcinia propinqua twigs
title_sort rearranged benzophenones and prenylated xanthones from garcinia propinqua twigs
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84867002348&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/51355
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