P. Gong

Lin Xie, Guang-Ji Wang, Hai-Ping Hao, 2011, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

Design, synthesis, and docking studies of phenylpicolinamide derivatives bearing 1H-pyrrolo[2,3-b]pyridine moiety as c-Met inhibitors.

Ping Gong, Min Wang, P. Gong, 2016, Bioorganic & medicinal chemistry.

Discovery of novel mutant-combating ALK and ROS1 dual inhibitors bearing imidazolidin-2-one moiety with reasonable PK properties.

X. Zhai, Nan Jiang, Daiying Zuo, 2019, European journal of medicinal chemistry.

Design, synthesis and structure-activity relationships of novel 4-phenoxyquinoline derivatives containing 1,2,4-triazolone moiety as c-Met kinase inhibitors.

Jinxing Hu, P. Gong, Yajing Liu, 2016, European journal of medicinal chemistry.

Beneficial estrogen-like effects of ginsenoside Rb1, an active component of Panax ginseng, on neural 5-HT disposition and behavioral tasks in ovariectomized mice.

Lin Xie, Guang-Ji Wang, Hai-Ping Hao, 2011, European journal of pharmacology.

Quantitative structure-ion intensity relationship strategy to the prediction of absolute levels without authentic standards.

Ping Gong, Guangji Wang, Guangji Wang, 2013, Analytica chimica acta.

Synthesis and cytotoxicity studies of quinoline-3-carbonitrile derivatives

X. Zhai, P. Gong, Hong Yu, 2010 .

Design, synthesis, and structure-activity relationships of novel imidazo[4,5-c]pyridine derivatives as potent non-nucleoside inhibitors of hepatitis C virus NS5B.

P. Gong, Yingxiu Li, Yajing Liu, 2018, Bioorganic & medicinal chemistry.

Discovery of novel 2,4-diarylaminopyrimidine analogues as ALK and ROS1 dual inhibitors to overcome crizotinib-resistant mutants including G1202R.

X. Zhai, Yucheng Gu, Daiying Zuo, 2018, European journal of medicinal chemistry.

Catalyst-Free Cyclization- and Curtius Rearrangement-Induced Functional Group Transformation: An Improved Synthetic Strategy of First-in-Class ATX Inhibitor Ziritaxestat (GLPG-1690)

X. Zhai, Nan Jiang, P. Gong, 2020 .

Design, synthesis and anticancer activity of 4-morpholinothieno[3,2-d]pyrimidine derivatives bearing arylmethylene hydrazine moiety.

X. Zhai, P. Gong, Wufu Zhu, 2012, Chemical & pharmaceutical bulletin.

Discovery and rational design of 2-aminopyrimidine-based derivatives targeting Janus kinase 2 (JAK2) and FMS-like tyrosine kinase 3 (FLT3).

P. Gong, Yanfang Zhao, Yingxiu Li, 2020, Bioorganic chemistry.

Design, synthesis, and biological evaluation of 4-phenoxyquinoline derivatives as potent c-Met kinase inhibitor.

P. Gong, Yanfang Zhao, Yingxiu Li, 2019, Bioorganic & medicinal chemistry letters.

Design, synthesis and biological evaluation of novel thieno[3,2-d]pyrimidine derivatives containing diaryl urea moiety as potent antitumor agents.

P. Gong, Dazhuang Zuo, Zijian Liu, 2014, European journal of medicinal chemistry.

Microsomal Cytochrome P450-Mediated Metabolism of Protopanaxatriol Ginsenosides: Metabolite Profile, Reaction Phenotyping, and Structure-Metabolism Relationship

Guangji Wang, H. Hao, Liang Wu, 2010, Drug Metabolism and Disposition.

Design, synthesis and antifungal activities of novel triazole derivatives with selenium-containing hydrophobic side chains.

Xin Wang, P. Gong, Chun Guo, 2022, Bioorganic & medicinal chemistry letters.

Design, synthesis, and biological evaluation of selenium-containing small molecule compounds based on the dual mechanism of fungal CYP51 inhibition and fungal ROS generation

Xin Wang, P. Gong, Xin Su, 2022, Journal of Molecular Structure.

Synthesis and antiproliferative activity of pyrrolo[2,3-b]pyridine derivatives bearing the 1,8-naphthyridin-2-one moiety.

Min Wang, P. Gong, Linxiao Wang, 2018, European journal of medicinal chemistry.

Syntheses and antiproliferative activities of novel diarylthiosemicarbazide derivatives

X. Zhai, Zhen Yang, P. Gong, 2013, Chemical Research in Chinese Universities.

Design, synthesis and antiproliferative activities of diaryl urea derivatives bearing N-acylhydrazone moiety

X. Zhai, Chunfu Wu, P. Gong, 2012 .

Anti‐Tumor Activity of New Artemisinin–Chalcone Hybrids

X. Zhai, P. Gong, Lijun Xie, 2011, Archiv der Pharmazie.

Antitumor Activity of New Artemisinin—Chalcone Hybrids.

Chongxing Liu, X. Zhai, P. Gong, 2012 .

(1R,3S,4R,4aS,7R,7aS,10R,12aR)-3-Azido-4,7,10-trimethyl-1,10-epidioxyperhydropyrano[4,3-j][1,2]benzodioxepine

X. Zhai, P. Gong, Lijun Xie, 2010, Acta crystallographica. Section E, Structure reports online.

Synthesis and Cytotoxic Evaluation of Some New Phthalazinylpiperazine Derivatives

P. Gong, Yajing Liu, Jianqiang Wang, 2012, Archiv der Pharmazie.

Synthesis and in‐vitro Anti‐hepatitis B Virus Activity of Ethyl 6‐Bromo‐8‐hydroxyimidazo[1,2‐a]pyridine‐3‐carboxylates

P. Gong, Dong Chen, Yajing Liu, 2011, Archiv der Pharmazie.

Synthesis and in vitro anti-hepatitis B virus activity of 1H-benzimidazol-5-ol derivatives

X. Zhai, P. Gong, Dong Chen, 2010 .

THE PURIFICATION AND CHARACTERIZATION OF USP30 by Jason Cargill A thesis submitted to the Faculty of the University of Delaware in partial fulfillment of the requirements for the degree of Master of Science in Chemistry and Biochemistry

C. Arighi, M. Johnston, Zhihao Zhuang, 2017 .

Design, synthesis and biological evaluation of novel 4-phenoxy-6,7-disubstituted quinolines possessing (thio)semicarbazones as c-Met kinase inhibitors.

X. Zhai, P. Gong, Limei Wang, 2016, Bioorganic & medicinal chemistry.

A novel process for developing a quantitative chromatographic fingerprint analysis method based on analytical quality by design: A case study of Xiaochaihu capsules

Hai-bin Qu, Xingchu Gong, P. Gong, 2023, Microchemical Journal.

Identification of hydrazone moiety-bearing aminopyrimidines as potent antitumor agents with selective inhibition of gefitinib-resistant H1975 cancer cells

P. Gong, Yanfang Zhao, Ye Tian, 2017 .

Design, synthesis and biological evaluation of novel pteridinone derivatives as potent dual inhibitors of PLK1 and BRD4

P. Gong, Yanfang Zhao, Yajing Liu, 2020 .

Design, Synthesis and Biological Evaluation of Novel 4‐Thiazolidinones Containing Indolin‐2‐one Moiety as Potential Antitumor Agent.

P. Gong, Yanfang Zhao, Guogang Zhang, 2011 .

Synthesis and Cytotoxicity Studies of Novel 2‐Hydrazonylpyrido[2,3‐b]pyrazin‐3(4H)‐ones

P. Gong, Yajing Liu, Guogang Zhang, 2012, Archiv der Pharmazie.

Microsomal Cytochrome P450-Mediated Metabolism of Protopanaxatriol Ginsenosides: Metabolite Profile, Reaction Phenotyping, and Structure-Metabolism Relationship

Guangji Wang, H. Hao, Liang Wu, 2010, Drug Metabolism and Disposition.

Design and Synthesis of Novel 4‐Phenoxyquinolines Bearing 3‐Hydrosulfonylacrylamido or 1H‐Imidazole‐4‐carboxamido Scaffolds as c‐Met Kinase Inhibitors

X. Zhai, P. Gong, Yu Wang, 2017, Archiv der Pharmazie.

Beneficial estrogen-like effects of ginsenoside Rb1, an active component of Panax ginseng, on neural 5-HT disposition and behavioral tasks in ovariectomized mice.

Lin Xie, Guang-Ji Wang, Hai-Ping Hao, 2011, European journal of pharmacology.

Palladium-catalyzed three-component tandem reaction of sulfonyl hydrazones, aryl iodides and allenes: highly stereoselective synthesis of (Z)-α-hydroxymethyl allylic sulfones

P. Gong, Yanfang Zhao, Mingze Qin, 2017 .

Synthesis and anti-tumor activity of 2-amino-3-cyano-6-(1H-indol-3-yl)-4-phenylpyridine derivatives in vitro.

Yucheng Gu, P. Gong, Yanfang Zhao, 2011, European journal of medicinal chemistry.

Characterization of the in vivo and in vitro metabolic profile of PAC-1 using liquid chromatography-mass spectrometry.

Xiaohui Chen, Kaishun Bi, P. Gong, 2008, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

Design, synthesis, and biological evaluation of novel substituted benzamide derivatives bearing a 1,2,3-triazole moiety as potent human dihydroorotate dehydrogenase inhibitors.

P. Gong, Yanfang Zhao, L. Cai, 2018, Bioorganic chemistry.