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32 articles for JW Strohbach


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

PMID
Cmpds
Data
Article Title
Organization
22
Inhibitors of the protease from human immunodeficiency virus: synthesis, enzyme inhibition, and antiviral activity of a series of compounds containing the dihydroxyethylene transition-state isostere.EBI
Upjohn Laboratories
11
Peptidomimetic HIV protease inhibitors: phosphate prodrugs with improved biological activities.EBI
Upjohn
16
Inhibitors of the protease from human immunodeficiency virus: design and modeling of a compound containing a dihydroxyethylene isostere insert with high binding affinity and effective antiviral activity.EBI
Upjohn
2
The design and development of 2-aryl-2-hydroxy ethylamine substituted 1H,7H-pyrido[1,2,3-de]quinoxaline-6-carboxamides as inhibitors of human cytomegalovirus polymerase.EBI
Pfizer
20
 
Synthesis and pharmacological evaluation of sulfone substituted HIV protease inhibitorsEBI
TBA
33
Discovery of a Series of Pyrimidine Carboxamides as Inhibitors of Vanin-1.EBI
Pfizer
8
Non-peptidic HIV protease inhibitors: C2-symmetry-based design of bis-sulfonamide dihydropyrones.EBI
Pharmacia & Upjohn
23
Structure-based design of HIV protease inhibitors: 5,6-dihydro-4-hydroxy-2-pyrones as effective, nonpeptidic inhibitors.EBI
Pharmacia & Upjohn
22
Cycloalkylpyranones and cycloalkyldihydropyrones as HIV protease inhibitors: exploring the impact of ring size on structure-activity relationships.EBI
Pharmacia and Upjohn
11
Rational approach to highly potent and selective apoptosis signal-regulating kinase 1 (ASK1) inhibitors.EBI
Pfizer
43
Identification of N-{cis-3-[Methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino]cyclobutyl}propane-1-sulfonamide (PF-04965842): A Selective JAK1 Clinical Candidate for the Treatment of Autoimmune Diseases.EBI
Pfizer
24
Discovery of Clinical Candidate 1-{[(2S,3S,4S)-3-Ethyl-4-fluoro-5-oxopyrrolidin-2-yl]methoxy}-7-methoxyisoquinoline-6-carboxamide (PF-06650833), a Potent, Selective Inhibitor of Interleukin-1 Receptor Associated Kinase 4 (IRAK4), by Fragment-Based Drug Design.EBI
Pfizer
32
AZA-ERGOLINE DERIVATIVE AND PREPARATION METHOD THEREFOR AND APPLICATION THEREOFBDB
Shanghaitech University
3
SUBSTITUTED TRICYCLIC COMPOUND AS PRMT5 INHIBITOR AND USE THEREOFBDB
NANJING SANHOME PHARMACEUTICAL CO., LTD.
74
COMPOUNDS AND METHODS FOR MODULATING FXRBDB
Terns Pharmaceuticals
98
5-AMINO-8-(4-PYRIDYL)-[1,2,4]TRIAZOLO[4,3-C]PYRIMIDIN-3-ONE COMPOUNDS FOR USE AGAINST CANCERBDB
AstraZeneca
51
Macrocyclic indoles as Mcl-1 inhibitorsBDB
Ascentage Pharma (Suzhou)
228
Substituted imidazo[1,5-a]pyrazines for IRE1 inhibitionBDB
Optikira
13
Pharmacophores, compounds and methods having application in the treatment of cancer through inhibition of CYP17A1 and CYP19A1BDB
Mangosuthu University of Technology
3
Substituted [1,2,4]triazolo[4,3-a]pyrazines as antidiabeticsBDB
King Abdulaziz University
7
Quinoline analogs as phosphatidylinositol 3-kinase inhibitorsBDB
Hangzhou Zhengxiang Pharmaceuticals
6
Lactam compounds as EP4 receptor-selective agonists for use in the treatment of EP4-mediated diseases and conditionsBDB
Cayman Chemical
65
Spirocyclic dihydro-thiazine and dihydro-oxazine BACE inhibitors, and compositions and uses thereofBDB
Imago Pharmaceuticals
97
Buprenorphine analogsBDB
Purdue Pharma
87
5-substituted indazoles as kinase inhibitorsBDB
Abbvie
24
Quarternized buprenorphine analogsBDB
Purdue Pharma
23
Discovery of new 4-alkoxyquinazoline-based derivatives as potent VEGFR2 inhibitors.BDB
Nanjing University
375
3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant IDHBDB
Novartis
16
Cloning, expression and pharmacology of the mouse 5-HT(4L) receptor.BDB
Cnrs Upr 9023
23
Arylpyrrolopyridine derived compounds as LRRK2 inhibitorsBDB
H. Lundbeck
66
BMP inhibitors and methods of use thereofBDB
The Brigham and Women'S Hospital
593
Combination of kinase inhibitors and uses thereofBDB
Intellikine