Xinying Qian
Chengdu, 610041, China
Last Updated: 09/26/2026
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Found 14 publications
Discovery of Highly Potent and Selective SOS1 Inhibitors for the Treatment of KRAS-Driven Colorectal Cancer.
Journal: Journal of medicinal chemistry
Published: June 05, 2026
NLRP3 Inhibitor KBD3536 Attenuates Acute Inflammation, Radiation-Induced Skin Injury, and Early Metabolic Dysfunction in Preclinical Models.
Journal: Pharmaceuticals (Basel, Switzerland)
Published: May 28, 2026
Discovery of novel and potent NLRP3 inflammasome inhibitors with new lipophilic moieties.
Journal: European journal of medicinal chemistry
Published: August 15, 2025
Discovery of KBD4466, a Selective TLR 7/8 Inhibitor, for the Treatment of Autoimmune Diseases.
Journal: Journal of medicinal chemistry
Published: July 01, 2025
Serine starvation suppresses the progression of esophageal cancer by regulating the synthesis of purine nucleotides and NADPH.
Journal: Cancer & metabolism
Published: March 25, 2024
Correction to "Bifunctional Naphtho[2,3-d][1,2,3]triazole-4,9-dione Compounds Exhibit Antitumor Effects In Vitro and In Vivo by Inhibiting Dihydroorotate Dehydrogenase and Inducing Reactive Oxygen Species Production".
Journal: Journal of medicinal chemistry
Published: September 14, 2020
Bifunctional Naphtho[2,3-d][1,2,3]triazole-4,9-dione Compounds Exhibit Antitumor Effects In Vitro and In Vivo by Inhibiting Dihydroorotate Dehydrogenase and Inducing Reactive Oxygen Species Production.
Journal: Journal of medicinal chemistry
Published: June 05, 2020
Design and biological evaluation of tetrahydropyridine derivatives as novel human GPR119 agonists.
Journal: Bioorganic & medicinal chemistry letters
Published: October 21, 2019
Lipidomic profiling reveals lipid regulation by a novel LSD1 inhibitor treatment.
Journal: Oncology reports
Published: October 02, 2019
Corrigendum to "ZY0511, a novel, potent and selective LSD1 inhibitor, exhibits anticancer activity against solid tumors via the DDIT4/mTOR pathway" [Cancer Lett. 454 (2019) 179-190].
Journal: Cancer letters
Published: May 20, 2019
ZY0511, a novel, potent and selective LSD1 inhibitor, exhibits anticancer activity against solid tumors via the DDIT4/mTOR pathway.
Journal: Cancer letters
Published: November 08, 2018
Last Updated: 09/26/2026