20 articles for V Patel
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Scaffold hopping towards potent and selective JAK3 inhibitors: discovery of novel C-5 substituted pyrrolopyrazines.

Hoffmann-La Roche
Discovery of a series of novel 5H-pyrrolo[2,3-b]pyrazine-2-phenyl ethers, as potent JAK3 kinase inhibitors.

Hoffmann-La Roche
Strategic use of conformational bias and structure based design to identify potent JAK3 inhibitors with improved selectivity against the JAK family and the kinome.

F. Hoffmann-La Roche
3-Amido pyrrolopyrazine JAK kinase inhibitors: development of a JAK3 vs JAK1 selective inhibitor and evaluation in cellular and in vivo models.

F. Hoffmann-La Roche
A Potent and Orally Efficacious, Hydroxyethylamine-Based Inhibitor of ß-Secretase.

TBA
Type II NADH dehydrogenase of the respiratory chain of Plasmodium falciparum and its inhibitors.

Harvard School of Public Health
Development of a fluorescence polarization based assay for histone deacetylase ligand discovery.

The Broad Institute of Harvard and Mit
Improvement of physiochemical properties of the tetrahydroazepinoindole series of farnesoid X receptor (FXR) agonists: beneficial modulation of lipids in primates.

Wyeth Research
Sulfonamido-aryl ethers as bradykinin B1 receptor antagonists.

Pharmacopeia
Peptide inhibitors of dengue virus NS3 protease. Part 2: SAR study of tetrapeptide aldehyde inhibitors.

Novartis Institute For Tropical Diseases
Peptide inhibitors of Dengue virus NS3 protease. Part 1: Warhead.

Novartis Institute For Tropical Diseases
Discovery, Characterization, and Structure-Based Optimization of Small-Molecule In Vitro and In Vivo Probes for Human DNA Polymerase Theta.

Artios Pharma
Development of single and mixed isoform selectivity PI3Kδ inhibitors by targeting Asn836 of PI3Kδ.

Monash University
Discovery of N-substituted 7-azaindoles as Pan-PIM kinases inhibitors - Lead optimization - Part III.

Sanofi
Maslinic and oleanolic acids derivatives for treating SARS-CoV-2 infection

King Abdulaziz University
Substituted N,2-diarylquinoline-4-carboxamides and the use thereof as anti-inflammatory agents

Bayer Pharma Aktiengesellschaft
Compounds, pharmaceutical composition and their use in treating neurodegenerative diseases

Universite De Lille 2 Droit Et Sante
Rapid parallel synthesis of dipeptide diphenyl phosphonate esters as inhibitors of dipeptidyl peptidases.

University of Anterwerp
Potent CYP19 (aromatase) 1-[(benzofuran-2-yl)(phenylmethyl)pyridine, -imidazole, and -triazole inhibitors: synthesis and biological evaluation.

Cardiff University