The first public molecular recognition database, BindingDB supports research, education and practice in drug discovery, pharmacology and related fields.

BindingDB contains 3.2M data for 1.4M Compounds and 11.4K Targets. Of those, 1.6M data for 756K Compounds and 4.8K Targets were curated by BindingDB curators. BindingDB is a FAIRsharing resource.

If BindingDB was of value to your research, please take a moment to donate to this nonprofit project. Your donation will let us provide you with more data and improved service.

To help with training and testing AI and other models, BindingDB downloads and search results now provide the publication date and BindingDB curation date of each measurement.

12 articles for J Pei


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

PMID
Data
Article Title
Organization
Discovering potent small molecule inhibitors of cyclophilin A using de novo drug design approach.EBI
East China University of Science and Technology
Discovery of multitarget inhibitors by combining molecular docking with common pharmacophore matching.EBI
Peking University
Design, Synthesis, and Biological Evaluation of Dual Inhibitors of EGFRL858R/T790M/ACK1 to Overcome Osimertinib Resistance in Nonsmall Cell Lung Cancers.EBI
Sichuan University
Design, Synthesis, and Antitumor Activity of Potent and Selective EGFR L858R/T790M Inhibitors and Identification of a Combination Therapy to Overcome Acquired Resistance in Models of Non-small-cell Lung Cancer.EBI
Sichuan University
Diaporaustalides A-L, Austalide Meroterpenoids from a Plant Endophytic EBI
Huazhong University of Science and Technology
Optimization of BAX trigger site activator BTSA1 with improved antitumor potency and in vitro ADMET properties.EBI
Shenyang Pharmaceutical University
Small Molecules Targeting Activated Cdc42-Associated Kinase 1 (ACK1/TNK2) for the Treatment of Cancers.EBI
National Clinical Research Center For Geriatrics
Discovery of Clinical Candidate NTQ1062 as a Potent and Bioavailable Akt Inhibitor for the Treatment of Human Tumors.EBI
Nanjing Chia-Tai Tianqing Pharmaceutical
Isatin compounds as noncovalent SARS coronavirus 3C-like protease inhibitors.EBI
Peking University
Unraveling the Design and Discovery of c-Jun N-Terminal Kinase Inhibitors and Their Therapeutic Potential in Human Diseases.EBI
National Clinical Research Center For Geriatrics
Progress of thrombus formation and research on the structure-activity relationship for antithrombotic drugs.EBI
Northwest University
COMBINATIONS OF CTPS1 AND BCL2 INHIBITORS FOR CANCERBDB
Step Pharma