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Ye Deng
Researcher at Ohio State University
Publications - 10
Citations - 303
Ye Deng is an academic researcher from Ohio State University. The author has contributed to research in topics: Traditional Chinese medicine & Sphenostylis. The author has an hindex of 8, co-authored 10 publications receiving 271 citations.
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Anthraquinones with quinone reductase-inducing activity and benzophenones from Morinda citrifolia (noni) roots
TL;DR: Two new benzophenones, morintrifolins A and B, together with 14 known anthraquinones and four other known compounds, were isolated from a chloroform-soluble extract of Morinda citrifolia roots, showing quinone reductase (QR)- inducing activity in Hepa lclc7 cells.
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Antioxidant and Quinone Reductase-Inducing Constituents of Black Chokeberry (Aronia melanocarpa) Fruits
TL;DR: Using in vitro hydroxyl radical-scavenging and quinone reductase-inducing assays, bioactivity-guided fractionation of an ethyl acetate-soluble extract of the fruits of the botanical dietary supplement, black chokeberry, led to the isolation of 27 compounds, including a new depside, ethyl 2-[(3,4- dihydroxybenzoyloxy)-4,6-dihydroxyphenyl].
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Potent antiprotozoal activity of a novel semi-synthetic berberine derivative
Mark Bahar,Ye Deng,Xiaohua Zhu,Shanshan He,Trupti Pandharkar,Mark E. Drew,Armando Navarro-Vázquez,Clemens Anklin,Roberto R. Gil,Raymond W. Doskotch,Karl A. Werbovetz,A. Douglas Kinghorn +11 more
TL;DR: A new semi-synthetic berberine analogue, 5,6-didehydro-8,8-diethyl-13-oxodihydroberberine chloride, showed nanomolar level potency against in vitro models of leishmaniasis, malaria, and trypanosomiasis as well as activity in an in vivo visceral leish maniasis model.
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Isolation, structure elucidation, and biological evaluation of 16,23-epoxycucurbitacin constituents from Eleaocarpus chinensis.
Li Pan,Yeonjoong Yong,Ye Deng,Daniel D. Lantvit,Tran Ngoc Ninh,Heebyung Chai,Esperanza J. Carcache de Blanco,Djaja D. Soejarto,Djaja D. Soejarto,Steven M. Swanson,A. Douglas Kinghorn +10 more
TL;DR: Elaeocarpucin C, produced by partial synthesis from 16α,23α-epoxy-3β,20β-dihydroxy-10αH,23βH-cucurbit-5,24-dien-11-one, was found to be inactive when evaluated in an in vivo hollow fiber assay using three different cancer cell types (dose range 0.5-10 mg/kg/day, i.p.).
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Phytochemical and bioactivity studies on constituents of the leaves of Vitex quinata
Ye Deng,Young-Won Chin,Heebyung Chai,Esperanza J. Carcache de Blanco,Leonardus B.S. Kardono,Soedarsano Riswan,Djaja D. Soejarto,Norman R. Farnsworth,A. Douglas Kinghorn +8 more
TL;DR: A phytochemical investigation of the leaves of Vitex quinata (Lour.) F.N. Williams (Verbenaceae) led to the isolation of a new δ-truxinate derivative and a new phytonoic acid derivative, together with 12 known compounds.