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.

25 articles for WL Cody


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

PMID
Data
Article Title
Organization
The discovery of fluoropyridine-based inhibitors of the factor VIIa/TF complex--Part 2.EBI
Pfizer
Design of a potent combined pseudopeptide endothelin-A/endothelin-B receptor antagonist, Ac-DBhg16-Leu-Asp-Ile-[NMe]Ile-Trp21 (PD 156252): examination of its pharmacokinetic and spectral properties.EBI
Warner-Lambert
Structure-activity relationships of C-terminal endothelin hexapeptide antagonists.EBI
Warner-Lambert
Design of a functional hexapeptide antagonist of endothelin.EBI
Warner-Lambert
 
Structure-activity and biophysical studies of the C-terminal hexapeptide of endothelinEBI
TBA
 
An efficient preparation of the potent and selective pseudopeptide thrombin inhibitor, inogatranEBI
TBA
 
Res-701-1, synthesis and a reevaluation of its effects on the endothelin receptorsEBI
TBA
 
Structure-activity relationships in a series of monocyclic endothelin analoguesEBI
TBA
 
Design of C-terminal peptide antagonists of endothelin: structure-activity relationships of ET-[16–21, D-His16]EBI
TBA
Exploration of 4,4-disubstituted pyrrolidine-1,2-dicarboxamides as potent, orally active Factor Xa inhibitors with extended duration of action.EBI
Pfizer
The discovery of fluoropyridine-based inhibitors of the Factor VIIa/TF complex.EBI
Pfizer
Rational design, synthesis, and biological activity of benzoxazinones as novel factor Xa inhibitors.EBI
Pfizer
The design of potent and selective inhibitors of thrombin utilizing a piperazinedione template: part 2.EBI
Warner-Lambert
The design of potent and selective inhibitors of thrombin utilizing a piperazinedione template: part 1.EBI
Warner-Lambert
N,N-dialkyl-dipeptidylamines as novel N-type calcium channel blockers.EBI
Warner-Lambert
Potent and selective bicyclic lactam inhibitors of thrombin: Part 3: P1' modifications.EBI
Warner-Lambert
Potent and selective bicyclic lactam inhibitors of thrombin: Part 2: P1 modifications.EBI
Warner-Lambert
Design of peptidomimetics that inhibit the association of phosphatidylinositol 3-kinase with platelet-derived growth factor-beta receptor and possess cellular activity.EBI
Warner-Lambert
Multiple binding modes for the receptor-bound conformations of cyclic AII agonists.EBI
Washington University
Structure-activity relationships of the potent combined endothelin-A/endothelin-B receptor antagonist Ac-DDip16-Leu-Asp-Ile-Ile-Trp21: development of endothelin-B receptor selective antagonists.EBI
Warner-Lambert
3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant IDHBDB
Novartis
Lactams as inhibitors of rockBDB
Bristol-Myers Squibb
Inhibitor of bruton's tyrosine kinaseBDB
Centaurus Biopharma
Substituted cyanoguanidines as oral anti-viralsBDB
Abbvie
Identification of 4-(2-(4-amino-1,2,5-oxadiazol-3-yl)-1-ethyl-7-{[(3S)-3-piperidinylmethyl]oxy}-1H-imidazo[4,5-c]pyridin-4-yl)-2-methyl-3-butyn-2-ol (GSK690693), a novel inhibitor of AKT kinase.BDB
Glaxosmithkline