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Jun Deguchi

Researcher at Hoshi University

Publications -  32
Citations -  460

Jun Deguchi is an academic researcher from Hoshi University. The author has contributed to research in topics: Cassia & Diarylheptanoids. The author has an hindex of 13, co-authored 31 publications receiving 408 citations. Previous affiliations of Jun Deguchi include Tokushima Bunri University.

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Cassiarins C−E, Antiplasmodial Alkaloids from the Flowers of Cassia siamea

TL;DR: Three new alkaloids, cassiarins C-E (1-3), and a new chromone, 10,11-dihydroanhydrobarakol (4), which showed moderate antiplasmodial activity against Plasmodium falciparum 3D7 were isolated from flowers of Cassia siamea, and the structures of 1-4 were elucidated by 2D NMR analysis and chemical transformation.
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Vasorelaxant effect of FR900359 from Ardisia crenata on rat aortic artery.

TL;DR: The results suggest that the vasorelaxant effect of FR900359 is mediated through the increased release of NO from endothelium-intact aortic cells at low concentrations, and can be attributed to inhibitory effects on voltage-dependent Ca2+ channel- and receptor-operated Ca2- channel-dependentCa2+ influx at high concentrations.
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Sucutiniranes A and B, new cassane-type diterpenes from Bowdichia nitida.

TL;DR: Two new cassane-type diterpenes, sucutiniranes A and B, have been isolated from the seeds of Bowdichia nitida together with 6alpha-acetoxyvouacapane and showed in vitro antiplasmodial activity against parasite Plasmodium falciparum 3D7.
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Cyclic diarylheptanoids as Na+-glucose cotransporter (SGLT) inhibitors from Acer nikoense.

TL;DR: Structural-activity relationship of acerogenin derivatives on inhibitory activity of SGLT as well as conformational analysis of 1 and 2 on the basis of J-resolved HMBC spectra and X-ray analysis were discussed.
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Synthesis and structure–activity relationships of cassiarin A as potential antimalarials with vasorelaxant activity

TL;DR: A series of a hydroxyl and a nitrogen-substituted derivatives and a dehydroxy derivative of 1 have been synthesized as having potent antimalarials against P. falciparum with vasodilator activity, which may reduce cytoadherence of pRBC to vascular endothelium.