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Yi Fu Guan

Researcher at Hong Kong Baptist University

Publications -  6
Citations -  129

Yi Fu Guan is an academic researcher from Hong Kong Baptist University. The author has contributed to research in topics: Radermachera & Justicia gendarussa. The author has an hindex of 3, co-authored 6 publications receiving 78 citations.

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Potent Inhibitor of Drug-Resistant HIV-1 Strains Identified from the Medicinal Plant Justicia gendarussa

TL;DR: Justicia gendarussa, a medicinal plant collected in Vietnam, was identified as a potent anti-HIV-1 active lead from the evaluation of over 4500 plant extracts and it was determined that the presence of a quinovopyranosyloxy group in the structure is likely essential to retain the high degree of anti-hIV activity of this type of compounds.
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Anti-HIV diphyllin glycosides from Justicia gendarussa.

TL;DR: In a search for new anti-HIV active leads from over several thousands of plant extracts, a potent plant lead is identified as Justicia gendarussa (Acanthaceae), a medicinal plant that has been used for the treatment of injury, arthritis and rheumatism in Asia.
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Bioassay-Guided Isolation and Structural Modification of the Anti-TB Resorcinols from Ardisia gigantifolia.

TL;DR: 15 derivatives of the CHCl3 extract of the leaves and stems of the medicinal plant Ardisia gigantifolia led to the isolation of two anti‐TB 5‐alkylresorcinols, and the distinct structure–activity correlations of the parent compound were elucidated based on these derivatives.
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In Vitro and in Vivo Antitumor Effects of Plant-Derived Miliusanes and Their Induction of Cellular Senescence

TL;DR: It is revealed that the antiproliferative properties of miliusanes in carcinoma cells were highly associated with the p21-dependent induction of cellular senescence, which is superior to the mainstay chemotherapeutics paclitaxel or fluorouracil.
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Bioactive Constituents from Radermachera boniana.

TL;DR: In this article, a bioassay-directed fractionation of the roots of Radermachera boniana Dop (Bignoniaceae) led to the isolation of 17 naphthalene-based quinones and related derivatives including radermacherones A (1), B (2) and C (6), radermaquinone (3), and radermacherol (5).