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Biswanath Dasgupta

Bio: Biswanath Dasgupta is an academic researcher from Institute of Medical Sciences, Banaras Hindu University. The author has contributed to research in topics: Coptisine & Verbenaceae. The author has an hindex of 7, co-authored 8 publications receiving 133 citations.
Topics: Coptisine, Verbenaceae, Apigenin, Acacetin, Protopine

Papers
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Journal ArticleDOI
TL;DR: Apigenin, acacetin and a new flavone glycoside, characterised as the methyl ester of ac acetin-7-0-glucuronide have been isolated from the flowers of Clerodendron infortunatum.
Abstract: Apigenin, acacetin and a new flavone glycoside, characterised as the methyl ester of acacetin-7-0-glucuronide have been isolated from the flowers of Clerodendron infortunatum.

32 citations

Journal ArticleDOI
TL;DR: In this article, a mixture of triterpenoid saponins was obtained from the stem bark of Symplocos spicata, which behaved as a pure compound in TLC and HPLC, but heterogeneity was suspected on the basis of chemical and NMR spectral data.

30 citations

Journal ArticleDOI
TL;DR: Dehydrocheilanthifoline, a phenolic protoberberine alkaloid has been isolated from the whole plant of Fumaria indica together with coptisine.

10 citations


Cited by
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Journal ArticleDOI
TL;DR: The aim of this review is to summarize the various naturally occurring chalcone compounds which have been isolated from different plants to initiate further pharmacobotanical, biotechnological and medicinal studies on the field of chal cone research.
Abstract: The aim of this review is to summarize the various naturally occurring chalcone compounds which have been isolated from different plants. Chalcones considered as obligate intermediated in flavonoid biosynthesis but they do not accumulate to appreciable degree in most plants. The largest number of natural chalcones has been isolated from species of the Leguminosae, Asteraceae and Moraceae families. Chalcone accumulating plants have often been used in traditional medicine and chalcones have therefore been studied and reported to possess many beneficial biological effects including anti-inflammatory, antimicrobial, antifungal, antioxidant, cytotoxic, antitumor and chemopreventive activities. Previously published reviews on this topic survey the biological activities of natural and synthetic chalcones but there are no comprehensive contributions on occurrence and biological activities of natural chalcones. The present study provides an overview of hydroxy or/and methoxy-substituted chalcones, methylated, prenylated, geranylated and other monomeric derivatives, chromeno- and furanochalcones, dimeric chalcones and dihydrochalcone derivatives focusing on their biosynthesis, natural sources and biological activities. On the basis of 608 references, this review covers the phytochemistry and biological activity of natural chalcones, describing 646 compounds have been appeared in the literature since 1975. The summary is aimed to initiate further pharmacobotanical, biotechnological and medicinal studies on the field of chalcone research. This contribution reviews some of the general aspects of naturally occurring chalcones including their chemical categories, focusing on plant sources and biological activities. The review covers the major works appeared in the literature from 1975 up to 2014, relating to 608 references and 646 compounds.

228 citations

Journal ArticleDOI
TL;DR: The structural variation of isoprenylated flavonoids, including the chalcones, flavones and flavonols, as well as their dihydro derivatives are reviewed in this paper.

212 citations

Book ChapterDOI
TL;DR: In this paper, all references to the occurrence of flavone and flavonol aglycones which have appeared from 1975 to 1980, and also include such earlier references as were overlooked in the relevant chapters of The Flavonoids' (1975).
Abstract: Most reports on the identification of known flavonoids in new plant sources as well as those on novel flavonoids naturally deal with the two most abundant classes, the flavones and flavonols. For this chapter we have listed all references to the occurrence of flavone and flavonol aglycones which have appeared from 1975 to 1980, and also include such earlier references as were overlooked in the relevant chapters of The Flavonoids’ (1975). Emphasis is given to the natural distribution of these compounds. The data are collected in Tables 4.1 and 4.2 which cite substances, plant sources and references. Since 1974, some 50 flavones and 60 flavonols with common substitution patterns have been described as novel compounds. Many are simply new methyl ethers of known compounds. The structures are arranged throughout the Tables by number and arrangement of substituents in ring A, followed by ring B. Wherever possible, the plant organs from which the compounds have been isolated are cited. In cases where authors have extracted the ‘whole plant’ or ‘aerial parts’, it does not necessarily follow that the compound is present in all parts, since these substances are often specifically located in certain organs only. In all cases where free aglycones are encountered, especially highly methylated flavonoids, it is likely that they occur externally, or are associated with secretory structures and are correlated with the production of other lipophilic secondary compounds, mainly of terpenoid origin.

174 citations

Journal ArticleDOI
TL;DR: In this article, the signal peaks of the protons on oxygen-bearing carbon atoms were analyzed for configurational determination of 2,3-dihydroxy and 2, 3,23- and 2.3,24-trihydroxy substituents in triterpenoids.

115 citations

Journal ArticleDOI
TL;DR: In this article, β-glucosyl esters of A-ring oxygenated 19α-hydroxyursolic acids were isolated from the leaves of Rubus microphyllus, R koehneanus, R trifidus and R medius.

108 citations