Xinyong A. Liu

State Key Laboratory Of Discovery And Utilization Of Functional Components In Traditional Chinese Medicine, Shandong Key Laboratory Of Druggability Optimization And Evaluation For Lead Compounds
Jinan, 250012, China

Last Updated: 09/26/2026

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Found 371 publications

Deep contrastive learning and single-cell kinetic analysis: dual-engine breakthroughs in genome-wide ligand discovery.

Deep contrastive learning and single-cell kinetic analysis: dual-engine breakthroughs in genome-wide ligand discovery.

Journal: Science bulletin

Published: August 14, 2026

Novel Mechanisms of SARS-CoV-2 Drug Resistance and Rational Design of Anti-Resistant Antivirals.

Novel Mechanisms of SARS-CoV-2 Drug Resistance and Rational Design of Anti-Resistant Antivirals.

Journal: Molecules (Basel, Switzerland)

Published: July 14, 2026

Research Progress and Challenges of Anti-monkeypox Virus Drugs Targeting F13 Protein.

Research Progress and Challenges of Anti-monkeypox Virus Drugs Targeting F13 Protein.

Journal: Journal of medicinal chemistry

Published: July 13, 2026

Targeted Degradation of Capsid by Host-Hijacking PROTAC Overcomes Drug Resistance.

Targeted Degradation of Capsid by Host-Hijacking PROTAC Overcomes Drug Resistance.

Journal: Journal of medicinal chemistry

Published: July 13, 2026

NIPBL::NACC1 fusion hepatic tumor: report of a case

NIPBL::NACC1 fusion hepatic tumor: report of a case

Journal: Zhonghua bing li xue za zhi = Chinese journal of pathology

Published: June 30, 2026

Discovery of pyridine formyl hydrazide derivatives as potent non-nucleoside RSV polymerase inhibitors.

Discovery of pyridine formyl hydrazide derivatives as potent non-nucleoside RSV polymerase inhibitors.

Journal: European journal of medicinal chemistry

Published: June 23, 2026

Rational design of dual-site NNRTIs based on 2,4,5-trisubstituted pyrimidine scaffold for potent inhibition of resistant HIV-1.

Rational design of dual-site NNRTIs based on 2,4,5-trisubstituted pyrimidine scaffold for potent inhibition of resistant HIV-1.

Journal: European journal of medicinal chemistry

Published: June 15, 2026

Discovery of piperazine-based multi-site occupying coronavirus Mpro inhibitors with potent and broad-spectrum antiviral activity.

Discovery of piperazine-based multi-site occupying coronavirus Mpro inhibitors with potent and broad-spectrum antiviral activity.

Journal: European journal of medicinal chemistry

Published: June 07, 2026

Pyridoimidazolyl Sulfonamide Compound 2: A Superior Dual-Acting Drug Candidate with Potent URAT1 Inhibition and Anti-Inflammatory Activity for Gout Management.

Pyridoimidazolyl Sulfonamide Compound 2: A Superior Dual-Acting Drug Candidate with Potent URAT1 Inhibition and Anti-Inflammatory Activity for Gout Management.

Journal: Journal of medicinal chemistry

Published: May 26, 2026

Associations between vaginal microecological status and high-risk human papillomavirus positivity in women from Eastern China: a retrospective cross-sectional study.

Associations between vaginal microecological status and high-risk human papillomavirus positivity in women from Eastern China: a retrospective cross-sectional study.

Journal: Frontiers in medicine

Published: May 25, 2026

Discovery of a Novel Thienopyrimidine Derivative as a Potent Dual URAT1/GLUT9 Inhibitor with Enhanced Urate-Lowering Efficacy, Superior Pharmacokinetics, and Favorable Safety Profile for Gout and Hyperuricemia.

Discovery of a Novel Thienopyrimidine Derivative as a Potent Dual URAT1/GLUT9 Inhibitor with Enhanced Urate-Lowering Efficacy, Superior Pharmacokinetics, and Favorable Safety Profile for Gout and Hyperuricemia.

Journal: Journal of medicinal chemistry

Published: May 06, 2026

Dual prodrugs of N4-hydroxycytidine with ProTide and ester modifications as anti-SARS-CoV-2 agents.

Dual prodrugs of N4-hydroxycytidine with ProTide and ester modifications as anti-SARS-CoV-2 agents.

Journal: European journal of medicinal chemistry

Published: May 05, 2026

Showing 1-12 of 371

Last Updated: 09/26/2026