Drug intelligence / Profile preview

XH-30

Development stage
Preclinical
Lead developer
China Pharmaceutical University
01

Overview

XH-30: sourced facts only. name: "Among these compounds, XH-30 exhibited significant PKMYT1 inhibitory activity (IC50 = 4.1 nM) and induced G2/M phase release in MDA-MB-231 cells (a P53-mutated TNBC cell line), demonstrating promising antitumor effects in vivo (TGI = 58%)." [PMID:41427887]; target: "Among these compounds, XH-30 exhibited significant PKMYT1 inhibitory activity (IC50 = 4.1 nM) and induced G2/M phase release in MDA-MB-231 cells (a P53-mutated TNBC cell line), demonstrating promising antitumor effects in vivo (TGI = 58%)." [PMID:41427887]; developer: "Jiangsu Key Laboratory of Drug Design and Optimization, Department of Medicinal Chemistry, China Pharmaceutical University, Nanjing 211198, China." [PMID:41427887]; stage: "Among these compounds, XH-30 exhibited significant PKMYT1 inhibitory activity (IC50 = 4.1 nM) and induced G2/M phase release in MDA-MB-231 cells (a P53-mutated TNBC cell line), demonstrating promising antitumor effects in vivo (TGI = 58%)." [PMID:41427887]

02

Targets

PKMYT1 (Protein kinase membrane associated tyrosine/threonine 1)

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