Zhipei Wu

发表

GluK1 antagonists from 6-(tetrazolyl)phenyl decahydroisoquinoline derivatives: in vitro profile and in vivo analgesic efficacy.

D. Clawson, P. Ornstein, S. Iyengar, 2013, Bioorganic & medicinal chemistry letters.

Cell Cycle and Biochemical Effects of PD 0183812 A POTENT INHIBITOR OF THE CYCLIN D-DEPENDENT KINASES CDK4 AND CDK6*

D. W. Fry, E. Dobrusin, W. Leopold, 2001 .

Discovery of N-(6-Fluoro-1-oxo-1,2-dihydroisoquinolin-7-yl)-5-[(3R)-3-hydroxypyrrolidin-1-yl]thiophene-2-sulfonamide (LSN 3213128), a Potent and Selective Nonclassical Antifolate Aminoimidazole-4-carboxamide Ribonucleotide Formyltransferase (AICARFT) Inhibitor Effective at Tumor Suppression in a Can

Brandon J. Margolis, S. Atwell, Matthew R. Lee, 2017, Journal of Medicinal Chemistry.

Cell Cycle and Biochemical Effects of PD 0183812

D. W. Fry, E. Dobrusin, W. Leopold, 2001, The Journal of Biological Chemistry.

Convergent Genomic Signatures of Cashmere Traits: Evidence for Natural and Artificial Selection

Wei Wang, G. Xie, Xinmei Li, 2023, International journal of molecular sciences.

High-performance liquid Chromatographic separation of the enantiomers of N-aryloxazolinones, N-aryl thiazolinones and their sulfur derivatives on a synthetic chiral stationary phase

Zhipei Wu, W. H. Pirkle, Michael E. Koscho, 1996 .

Characterization of a novel AICARFT inhibitor which potently elevates ZMP and has anti-tumor activity in murine models

P. Iversen, Y. Qian, Matthew R. Lee, 2018, Scientific Reports.

GluK1 antagonists from 6-(carboxy)phenyl decahydroisoquinoline derivatives. SAR and evaluation of a prodrug strategy for oral efficacy in pain models.

P. Ornstein, S. Iyengar, M. del Prado, 2013, Bioorganic & medicinal chemistry letters.

Two prodrugs of potent and selective GluR5 kainate receptor antagonists actives in three animal models of pain.

P. Ornstein, S. Iyengar, M. del Prado, 2005, Journal of medicinal chemistry.

2-Substituted Aminopyrido[2,3- d ]pyrimidin-7(8 H )-ones. Structure−Activity Relationships Against Selected Tyrosine Kinases and in Vitro and in Vivo Anticancer Activity

D. Boschelli, A. Doherty, H. D. Showalter, 1998 .

Synthesis and structure-activity relationships of novel dipeptides and reduced dipeptides as ligands for melanocortin subtype-4 receptor.

P. Ornstein, K. Briner, M. J. Fisher, 2006, Bioorganic & medicinal chemistry letters.

Convergent molecular evolution of thermogenesis and circadian rhythm in Arctic ruminants

W. Wang, Shanlin Liu, Xinmei Li, 2023, Proceedings of the Royal Society B.

Characterization of a novel AICARFT inhibitor which potently elevates ZMP and has anti-tumor activity in murine models

P. Iversen, Y. Qian, Matthew R. Lee, 2018, Scientific Reports.

Pyrido[2,3-d]pyrimidin-7-one inhibitors of cyclin-dependent kinases.

D. Boschelli, D. W. Fry, S. Trumpp-Kallmeyer, 2000, Journal of medicinal chemistry.

Chromatin accessibility memory of donor cells disrupts bovine somatic cell nuclear transfer blastocysts development

Jingcheng Zhang, Yong Zhang, Y. Wang, 2023, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Green Synthesis of Liquid Crystal Intermediates the Preparation of Phenylacetylenes in Ionic Liquids

Bao-You Liu, F. Wei, Huilong Yang, 2010 .