R
Raghunath S. Thakur
Researcher at Central Institute of Medicinal and Aromatic Plants
Publications - 91
Citations - 2227
Raghunath S. Thakur is an academic researcher from Central Institute of Medicinal and Aromatic Plants. The author has contributed to research in topics: Costus & Artemisia annua. The author has an hindex of 22, co-authored 91 publications receiving 2138 citations.
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Carbon-13 NMR spectroscopy of steroidal sapogenins and steroidal saponins
TL;DR: The 13 C NMR chemical shifts of 130 naturally occurring steroidal sapogenins and saponin derivatives published up to 1983 are listed and a number of methods for signal assignment are explained as discussed by the authors.
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Antihepatotoxic principles of Phyllanthus niruri herbs.
K. V. Syamasundar,Bikram Singh,Raghunath S. Thakur,Akhtar Husain,Kiso Yoshinobu,Hikino Hiroshi +5 more
TL;DR: Among phyllanthin, hypophyllanth in, triacontanal and tricontanol isolated from a hexane extract of Phyllanthus niruri, phyll anthin and hypophyLLanthin protected against carbon tetrachloride- and galactosamine-induced cytotoxicity in primary cultured rat hepatocytes.
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13C NMR Spectroscopy of lignan and neolignan derivatives
TL;DR: In this article, 13C NMR shielding data for about 300 compounds are tabulated, and critical spectral features are discussed as a guide to the use of the technique in structure elucidation and stereochemical allocations of lignan, neolignan and their derivatives.
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Occurrence of some antiviral sterols in Artemisia annua
TL;DR: Out of the twenty one medicinal plants evaluated for their virus inhibitoryactivity against tobamoviruses on their test hosts reacting hypersensitively, extracts of Lawsonia alba, Artemisia annua and Cornus capitata showed high virus inhibitories activity.
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Biosynthesis of artemisinin in Artemisia annua
TL;DR: The isotope ratios (3 H: 14 C) in arteannuin B and artemisinin biosynthesized in Artemisia annua from [4 R - 3 H 1,2- 14 C]-, [5- 3 H 2,2 - 14 C]- and [2- 3H 2,2-14 C]- have revealed that two specific 1,2hydride shifts take place during the oxidation and lactonization of the germacrane skeleton to yield dihydrocostunolide as mentioned in this paper.