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Zhengtao Wang

Researcher at Shanghai University

Publications -  655
Citations -  13972

Zhengtao Wang is an academic researcher from Shanghai University. The author has contributed to research in topics: Medicine & Chemistry. The author has an hindex of 48, co-authored 586 publications receiving 10842 citations. Previous affiliations of Zhengtao Wang include London Metropolitan University & Chinese Ministry of Education.

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Antioxidant phenolic compounds from walnut kernels (Juglans regia L.)

TL;DR: In this paper, an activity-directed fractionation and purification process was used to isolate 1,1-diphenyl-2-picrylhydrazyl radical (DPPH) scavenging components from Juglans regia kernels.
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Bile acid nuclear receptor FXR and digestive system diseases

TL;DR: Current knowledge of the roles of FXR in physiology of the digestive system and the related diseases is discussed, with a focus on inflammatory bowel disease, colorectal cancer and type 2 diabetes.
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Advancement in analysis of Salviae miltiorrhizae Radix et Rhizoma (Danshen).

TL;DR: This review summarizes the recent advances in the chemical analysis of Danshen and its finished products, including the introduction of the identified bioactive components, analytical methods for quantitative determination of target analytes and fingerprinting authentication, quality criteria ofDanshen crude herb and its preparations, as well as the pharmacokinetic and pharmacodynamic studies on the active components of DANShen andIts finished products.
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Caffeic acid prevents acetaminophen-induced liver injury by activating the Keap1-Nrf2 antioxidative defense system

TL;DR: It is demonstrated that CA prevented APAP-induced hepatotoxicity by decreasing Keap1 expression, inhibiting binding of Keap 1 to NRF2, and thus activating Nrf2 and leading to increased expression of antioxidative signals including HO-1 and NQO1.
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In vitro anti-tumor activity of isorhamnetin isolated from Hippophae rhamnoides L. against BEL-7402 cells.

TL;DR: The cytotoxic effects of isorhamnetin showed dose- and time-dependency against human hepatocellular carcinoma cells (BEL-7402) with the appearance of a hypodiploid peak (sub-G(0)/G(1) peak), probably due to the presence of cells in apoptosis and apoptotic bodies with DNA content less than 2n.