17 articles for JG Varnes
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Optimization of Highly Kinase Selective Bis-anilino Pyrimidine PAK1 Inhibitors.

Astrazeneca
Towards the next generation of dual Bcl-2/Bcl-xL inhibitors.

Astrazeneca
Structure-activity relationship and pharmacokinetic profile of 5-ketopyrazole factor Xa inhibitors.

Bristol-Myers Squibb Research and Development
Discovery of novel positive allosteric modulators of the metabotropic glutamate receptor 5 (mGlu5).

Astrazeneca Pharmaceuticals
Design, structure-activity relationship, and pharmacokinetic profile of pyrazole-based indoline factor Xa inhibitors.

Bristol-Myers Squibb Pharmaceutical Research Institute
CC chemokine receptor-3 (CCR3) antagonists: improving the selectivity of DPC168 by reducing central ring lipophilicity.

Bristol-Myers Squibb Pharmaceutical Research Institute
Discovery of (R)-9-ethyl-1,3,4,10b-tetrahydro-7-trifluoromethylpyrazino[2,1-a]isoindol- 6(2H)-one, a selective, orally active agonist of the 5-HT(2C) receptor.

Pharmaceutical Research Institute
Discovery of 5-{4-[(7-Ethyl-6-oxo-5,6-dihydro-1,5-naphthyridin-3-yl)methyl]piperazin-1-yl}-

Astrazeneca
Discovery of a Series of 7-Azaindoles as Potent and Highly Selective CDK9 Inhibitors for Transient Target Engagement.

Astrazeneca
Discovery of N-propylurea 3-benzylpiperidines as selective CC chemokine receptor-3 (CCR3) antagonists.

Bristol-Myers Squibb Pharmaceutical Research Institute
Addition of Fluorine and a Late-Stage Functionalization (LSF) of the Oral SERD AZD9833.

Astrazeneca
CCR3 antagonists: a potential new therapy for the treatment of asthma. Discovery and structure-activity relationships.

Bristol-Myers Squibb
Discovery of AZD4573, a Potent and Selective Inhibitor of CDK9 That Enables Short Duration of Target Engagement for the Treatment of Hematological Malignancies.

Astrazeneca
Fragment-assisted hit investigation involving integrated HTS and fragment screening: Application to the identification of phosphodiesterase 10A (PDE10A) inhibitors.

Astrazeneca
Bicyclo((aryl)methyl)benzamides as inhibitors of GlyT1.

Astrazeneca
Substituted N-phenethyltriazoloneacetamides and use thereof

Bayer Intellectual Property
Heterocyclic compounds containing an indole core

Boehringer Ingelheim International