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Zhihui Zhou

Researcher at Jiangxi Science and Technology Normal University

Publications -  8
Citations -  69

Zhihui Zhou is an academic researcher from Jiangxi Science and Technology Normal University. The author has contributed to research in topics: Apoptosis & Lead compound. The author has an hindex of 3, co-authored 8 publications receiving 17 citations.

Papers
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The new opportunities in medicinal chemistry of fourth-generation EGFR inhibitors to overcome C797S mutation

TL;DR: The recent advances in medicinal chemistry of fourth-generation EGFR-TKIs are discussed, as well as further discussed the clinical challenges and future prospects of treating patients with EGFR mutations resistant to third-generationEGFR- TKIs.
Journal ArticleDOI

Design, synthesis and antitumor activity of novel thiophene-pyrimidine derivatives as EGFR inhibitors overcoming T790M and L858R/T790M mutations

TL;DR: Five series of novel thiophene-pyrimidine derivatives synthesized and tested for their anti-proliferative activity against several cancer cell lines in which EGF is highly expressed showed excellent activity against one or more cancer cell Lines.
Journal ArticleDOI

Discovery of thiapyran-pyrimidine derivatives as potential EGFR inhibitors.

TL;DR: Cell cycle and apoptosis analysis suggested that 13a could block cancer cells in G2/M phase and induce into late apoptosis in a manner of concentration-dependent, and structure-activity relationship of 13a was analyzed to explore its mechanism.
Journal ArticleDOI

Design, synthesis and evaluation of anti-proliferative activity of 2-aryl-4-aminoquinazoline derivatives as EGFR inhibitors.

TL;DR: In this article, a class of 2-aryl-4-aminoquinazoline derivatives (7a-7j, 8a-8h, 9a-9h and 10a-10k) were designed, synthesized and evaluated as EGFR inhibitors.
Patent

Pyrimidine compound containing substituted phenyl acrylamide structure and application of compound

TL;DR: In this paper, a pyrimidine compound containing a substituted phenyl acrylamide structure, a geometric isomer of the compound, and pharmaceutically acceptable salts, hydrates, solvates or prodrugs is presented.