Bioactive flavonoids of the flowers of Butea monosperma

One new dihydrochalcone, dihydromonospermoside (7), was isolated from the flowers of Butea monosperma together with three known chalcones, butein (2), monospermoside (4) and isoliquiritigenin (8), one flavone, 7,3',4'- trihydroxyflavone (6), four flavanones, (-)-butin (1a), (-)-butrin (3a)...

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Main Authors: Ratchanaporn Chokchaisiri, Channarong Suaisom, Siriluk Sriphota, Anon Chindaduang, Thipphawan Chuprajob, Apichart Suksamrarn
Other Authors: Mahidol University
Format: Article
Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/27424
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spelling th-mahidol.274242018-09-13T14:12:51Z Bioactive flavonoids of the flowers of Butea monosperma Ratchanaporn Chokchaisiri Channarong Suaisom Siriluk Sriphota Anon Chindaduang Thipphawan Chuprajob Apichart Suksamrarn Mahidol University Thailand National Science and Technology Development Agency Chemistry Pharmacology, Toxicology and Pharmaceutics One new dihydrochalcone, dihydromonospermoside (7), was isolated from the flowers of Butea monosperma together with three known chalcones, butein (2), monospermoside (4) and isoliquiritigenin (8), one flavone, 7,3',4'- trihydroxyflavone (6), four flavanones, (-)-butin (1a), (-)-butrin (3a), (+)-isomonospermoside (5b) and (-)-liquiritigenin (9a), and three isoflavones, formononetin (10), afrormosin (11) and formononetin-7-O-β-D-glu- copyranoside (12). The structure of the new compound was elucidated by spectroscopic techniques whereas those of the known compounds were identified by comparisons of spectroscopic and some physical data with those of reported compounds. The absolute configurations at the 2-position of the flavanones 1a, 3a, 5b and 9a were established to be 2S, 2S, 2R and 2S, respectively, by circular dichroism spectral measurements and were confirmed by comparison of the optical rotations with those of reported values and by enzymic hydrolysis of the glucosides to the corresponding aglycones. The isolated flavonoids exhibited varying antimycobacterial activity with the chalcone 2 being the most active compound (MIC 12.5 μg/ml). © 2009 Pharmaceutical Society of Japan. 2018-09-13T06:31:57Z 2018-09-13T06:31:57Z 2009-04-30 Article Chemical and Pharmaceutical Bulletin. Vol.57, No.4 (2009), 428-432 10.1248/cpb.57.428 13475223 00092363 2-s2.0-65349113642 https://repository.li.mahidol.ac.th/handle/123456789/27424 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=65349113642&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Chemistry
Pharmacology, Toxicology and Pharmaceutics
spellingShingle Chemistry
Pharmacology, Toxicology and Pharmaceutics
Ratchanaporn Chokchaisiri
Channarong Suaisom
Siriluk Sriphota
Anon Chindaduang
Thipphawan Chuprajob
Apichart Suksamrarn
Bioactive flavonoids of the flowers of Butea monosperma
description One new dihydrochalcone, dihydromonospermoside (7), was isolated from the flowers of Butea monosperma together with three known chalcones, butein (2), monospermoside (4) and isoliquiritigenin (8), one flavone, 7,3',4'- trihydroxyflavone (6), four flavanones, (-)-butin (1a), (-)-butrin (3a), (+)-isomonospermoside (5b) and (-)-liquiritigenin (9a), and three isoflavones, formononetin (10), afrormosin (11) and formononetin-7-O-β-D-glu- copyranoside (12). The structure of the new compound was elucidated by spectroscopic techniques whereas those of the known compounds were identified by comparisons of spectroscopic and some physical data with those of reported compounds. The absolute configurations at the 2-position of the flavanones 1a, 3a, 5b and 9a were established to be 2S, 2S, 2R and 2S, respectively, by circular dichroism spectral measurements and were confirmed by comparison of the optical rotations with those of reported values and by enzymic hydrolysis of the glucosides to the corresponding aglycones. The isolated flavonoids exhibited varying antimycobacterial activity with the chalcone 2 being the most active compound (MIC 12.5 μg/ml). © 2009 Pharmaceutical Society of Japan.
author2 Mahidol University
author_facet Mahidol University
Ratchanaporn Chokchaisiri
Channarong Suaisom
Siriluk Sriphota
Anon Chindaduang
Thipphawan Chuprajob
Apichart Suksamrarn
format Article
author Ratchanaporn Chokchaisiri
Channarong Suaisom
Siriluk Sriphota
Anon Chindaduang
Thipphawan Chuprajob
Apichart Suksamrarn
author_sort Ratchanaporn Chokchaisiri
title Bioactive flavonoids of the flowers of Butea monosperma
title_short Bioactive flavonoids of the flowers of Butea monosperma
title_full Bioactive flavonoids of the flowers of Butea monosperma
title_fullStr Bioactive flavonoids of the flowers of Butea monosperma
title_full_unstemmed Bioactive flavonoids of the flowers of Butea monosperma
title_sort bioactive flavonoids of the flowers of butea monosperma
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/27424
_version_ 1763491556790108160