13 articles for JA Heath
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Identification of 4-piperazin-1-yl-quinazoline template based aryl and benzyl thioureas as potent, selective, and orally bioavailable inhibitors of platelet-derived growth factor (PDGF) receptor.

In Vivo Sciences Millennium Pharmaceuticals
Discovery of novel 2,8-diazaspiro[4.5]decanes as orally active glycoprotein IIb-IIIa antagonists.

Millennium Pharmaceuticals
Spirocyclic nonpeptide glycoprotein IIb-IIIa antagonists. Part 3: synthesis and SAR of potent and specific 2,8-diazaspiro[4.5]decanes.

Cor Therapeutics
3-aryl- heteroaryl substituted 5-trifluoromethyl oxadiazoles as histonedeacetylase 6 (HDAC6) inhibitors

Merck Sharp & Dohme
Pyridazine derivatives as RORc modulators

Genentech
Fused tricyclic ring derivatives as SRC homology-2 phosphatase inhibitors

Nikang Therapeutics
Bicyclic heteroaryl substituted compounds

Bristol-Myers Squibb
Structure of REV-ERBß ligand-binding domain bound to a porphyrin antagonist.

The Scripps Research Institute
The Parkinson disease-linked LRRK2 protein mutation I2020T stabilizes an active state conformation leading to increased kinase activity.

Harvard Neurodiscovery Center
New cholinesterase inhibitors for Alzheimer's disease: Structure Activity Studies (SARs) and molecular docking of isoquinolone and azepanone derivatives.

Universidade De Evora
Discovery of a Highly Selective STK16 Kinase Inhibitor.

Chinese Academy of Sciences
Inhibition of small ubiquitin-like modifier enzymes with substituted pyrrolo[2,3-b]quinoxalines

City of Hope
Inhibition of arginine aminopeptidase by bestatin and arphamenine analogues. Evidence for a new mode of binding to aminopeptidases.

University of Wisconsin