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BindingDB contains 3.2M data for 1.4M Compounds and 11.4K Targets. Of those, 1.6M data for 745K Compounds and 4.7K Targets were curated by BindingDB curators. BindingDB is a FAIRsharing resource.

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27 articles for P Ren


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Data
Article Title
Organization
Synthesis and biological evaluation of pyrido[2,3-d]pyrimidine-2,4-dione derivatives as eEF-2K inhibitors.EBI
The University of Texas At Austin
From in Silico Discovery to intra-Cellular Activity: Targeting JNK-Protein Interactions with Small Molecules.EBI
TBA
A type-II kinase inhibitor capable of inhibiting the T315I"gatekeeper" mutant of Bcr-Abl.EBI
Harvard Medical School
Discovery of pyrimidine benzimidazoles as Src-family selective Lck inhibitors. Part II.EBI
Genomics Institute of The Novartis Research Foundation
Discovery of pyrimidine benzimidazoles as Lck inhibitors: part I.EBI
Genomics Institute of The Novartis Research Foundation
Unleashing the Potential of 1,3-Diketone Analogues as Selective LH2 Inhibitors.EBI
University of Texas At Austin
Discovery, synthesis and mechanism study of 2,3,5-substituted [1,2,4]-thiadiazoles as covalent inhibitors targeting 3C-Like protease of SARS-CoV-2.EBI
Shanghaitech University
Discovery and Mechanism Study of SARS-CoV-2 3C-like Protease Inhibitors with a New Reactive Group.EBI
Shanghaitech University
Synthesis of iodinated 3beta-aryltropanes with selective binding to either the dopamine or serotonin transporters.EBI
State University of New York
Synthesis of 2beta-acyl-3beta-(substituted naphthyl)-8-azabicyclo[3.2.1]octanes and their binding affinities at dopamine and serotonin transport sites.EBI
State University of New York
Synthesis and monoamine transporter affinity of 3beta-(4-(2-pyrrolyl)phenyl)-8-azabicycl.EBI
State University of New York
Discovery, Optimization, and Evaluation of Potent and Highly Selective PI3Kγ-PI3Kδ Dual Inhibitors.EBI
Hutchison Medipharma
Stabilized β-Hairpin Peptide Inhibits Insulin Degrading Enzyme.EBI
Peking University Shenzhen Graduate School
Discovery of a potent inhibitor of MELK that inhibits expression of the anti-apoptotic protein Mcl-1 and TNBC cell growth.EBI
The University of Texas At Austin
NONMUSCLE MYOSIN II INHIBITORSBDB
University of Florida Research Foundation
NEW BENZODIAZEPINE DERIVATIVES AS GABA A GAMMA1 PAMBDB
Hoffmann-La Roche
Uses of a lysyl oxidase-like 2 inhibitorBDB
Pharmakea
Pharmaceutical compoundsBDB
Pfizer
BTK inhibitor compoundsBDB
Eli Lilly
Quinazoline derivative and preparation method thereforBDB
Chia Tai Tianqing Pharmaceutical Group
DYRK1 inhibitors and uses thereofBDB
Diaxonhit
Pharmacologically active compoundsBDB
Cancer Research Technology
Acid addition salt of substituted pyridine compoundBDB
Daiichi Sankyo
Imidazo[1,2-B][1,2,4]triazines as c-Met inhibitorsBDB
Incyte Holdings
Nitrogen-containing compounds and pharmaceutical compositions thereof for the treatment of atrial fibrillationBDB
Otsuka Pharmaceutical
Inhibitors of tumor progression loci-2 (Tpl2) kinase and tumor necrosis factor alpha (TNF-alpha) production: selectivity and in vivo antiinflammatory activity of novel 8-substituted-4-anilino-6-aminoquinoline-3-carbonitriles.BDB
Wyeth Research