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Zhili Zuo

Researcher at Chinese Academy of Sciences

Publications -  88
Citations -  1555

Zhili Zuo is an academic researcher from Chinese Academy of Sciences. The author has contributed to research in topics: Virtual screening & Docking (molecular). The author has an hindex of 20, co-authored 80 publications receiving 1247 citations. Previous affiliations of Zhili Zuo include Singapore Polytechnic & Sichuan University of Science and Engineering.

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Gambogic acid inhibits the catalytic activity of human topoisomerase IIα by binding to its ATPase domain

TL;DR: The results reported here show that GA exerts its antiproliferative effect by inhibiting the catalytic activity Topo IIα, and indicate that GA inhibits TopO IIα-mediated DNA cleavage and modulate the activity of Topo I poisons, which provide rationale for further clinical evaluation of GA.
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Melokhanines A–J, Bioactive Monoterpenoid Indole Alkaloids with Diverse Skeletons from Melodinus khasianus

TL;DR: Alkaloids 1-16, 25-27, 31, and 32 showed the best antibacterial activity against Pseudomonas aeruginosa and among the seven dermatophytes tested, compound 1 showed significant inhibitory activity against Microsporum canis, M. ferrugineum, and Trichophyton ajelloi.
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Discovery of Novel Small Molecule Inhibitors of Dengue Viral NS2B-NS3 Protease Using Virtual Screening and Scaffold Hopping

TL;DR: 17 new compounds were discovered as NS2B-NS3 protease inhibitors with IC(50) values of 7.46 ± 1.15 to 48.59 ± 3.46 μM, and 8 compounds belonging to two different scaffolds are active to some extent against DENV based on luciferase reporter replicon-based assays.
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Antitumor Research on Artemisinin and Its Bioactive Derivatives

TL;DR: This review concentrated on the new advances and development of artemisinin and its derivatives as potential antitumor agents in recent 5 years and it is hoped that this review could be helpful for further exploration of novel art Artemisinin-related antitumour agents.
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Two New Classes of T-Type Calcium Channel Inhibitors with New Chemical Scaffolds from Ganoderma cochlear.

TL;DR: Biological evaluation found that compounds (+)-1, (-)-3, and (±)-6 significantly inhibited Cav3.1 TTCC and showed noticeable selectivity against Cav1.2, Cav2.1, and Kv11.1 (hERG) channels.