32 articles for JW Strohbach
The following articles (labelled with PubMed ID or TBD) are for your review
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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.

Upjohn Laboratories
11
Peptidomimetic HIV protease inhibitors: phosphate prodrugs with improved biological activities.

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.

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.

Pfizer
20
Synthesis and pharmacological evaluation of sulfone substituted HIV protease inhibitors

TBA
33
Discovery of a Series of Pyrimidine Carboxamides as Inhibitors of Vanin-1.

Pfizer
8
Non-peptidic HIV protease inhibitors: C2-symmetry-based design of bis-sulfonamide dihydropyrones.

Pharmacia & Upjohn
23
Structure-based design of HIV protease inhibitors: 5,6-dihydro-4-hydroxy-2-pyrones as effective, nonpeptidic inhibitors.

Pharmacia & Upjohn
22
Cycloalkylpyranones and cycloalkyldihydropyrones as HIV protease inhibitors: exploring the impact of ring size on structure-activity relationships.

Pharmacia and Upjohn
11
Rational approach to highly potent and selective apoptosis signal-regulating kinase 1 (ASK1) inhibitors.

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.

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.

Pfizer
32
AZA-ERGOLINE DERIVATIVE AND PREPARATION METHOD THEREFOR AND APPLICATION THEREOF

Shanghaitech University
3
SUBSTITUTED TRICYCLIC COMPOUND AS PRMT5 INHIBITOR AND USE THEREOF

NANJING SANHOME PHARMACEUTICAL CO., LTD.
74
COMPOUNDS AND METHODS FOR MODULATING FXR

Terns Pharmaceuticals
98
5-AMINO-8-(4-PYRIDYL)-[1,2,4]TRIAZOLO[4,3-C]PYRIMIDIN-3-ONE COMPOUNDS FOR USE AGAINST CANCER

AstraZeneca
51
Macrocyclic indoles as Mcl-1 inhibitors

Ascentage Pharma (Suzhou)
228
Substituted imidazo[1,5-a]pyrazines for IRE1 inhibition

Optikira
13
Pharmacophores, compounds and methods having application in the treatment of cancer through inhibition of CYP17A1 and CYP19A1

Mangosuthu University of Technology
3
Substituted [1,2,4]triazolo[4,3-a]pyrazines as antidiabetics

King Abdulaziz University
7
Quinoline analogs as phosphatidylinositol 3-kinase inhibitors

Hangzhou Zhengxiang Pharmaceuticals
6
Lactam compounds as EP4 receptor-selective agonists for use in the treatment of EP4-mediated diseases and conditions

Cayman Chemical
65
Spirocyclic dihydro-thiazine and dihydro-oxazine BACE inhibitors, and compositions and uses thereof

Imago Pharmaceuticals
97
Buprenorphine analogs

Purdue Pharma
87
5-substituted indazoles as kinase inhibitors

Abbvie
24
Quarternized buprenorphine analogs

Purdue Pharma
23
Discovery of new 4-alkoxyquinazoline-based derivatives as potent VEGFR2 inhibitors.

Nanjing University
375
3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant IDH

Novartis
16
Cloning, expression and pharmacology of the mouse 5-HT(4L) receptor.

Cnrs Upr 9023
23
Arylpyrrolopyridine derived compounds as LRRK2 inhibitors

H. Lundbeck
66
BMP inhibitors and methods of use thereof

The Brigham and Women'S Hospital
593
Combination of kinase inhibitors and uses thereof

Intellikine