16 articles for JL Buchanan
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
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Article Title
Organization
Development of novel dual binders as potent, selective, and orally bioavailable tankyrase inhibitors.

Amgen
Discovery and hit-to-lead optimization of pyrrolopyrimidines as potent, state-dependent Na(v)1.7 antagonists.

Amgen
Discovery and optimization of a novel series of N-arylamide oxadiazoles as potent, highly selective and orally bioavailable cannabinoid receptor 2 (CB2) agonists.

Amgen
Structure-based design and synthesis of a novel class of Src SH2 inhibitors.

Ariad Pharmaceuticals
Discovery and optimization of aminopyrimidinones as potent and state-dependent Nav1.7 antagonists.

Amgen
Identification of a potent, state-dependent inhibitor of Nav1.7 with oral efficacy in the formalin model of persistent pain.

Amgen
Discovery of 2,4-bis-arylamino-1,3-pyrimidines as insulin-like growth factor-1 receptor (IGF-1R) inhibitors.

Amgen
Structural modifications of N-arylamide oxadiazoles: Identification of N-arylpiperidine oxadiazoles as potent and selective agonists of CB2.

Amgen
Discovery of 4-amino-5,6-biaryl-furo[2,3-d]pyrimidines as inhibitors of Lck: development of an expedient and divergent synthetic route and preliminary SAR.

Amgen
Discovery of aminoquinazolines as potent, orally bioavailable inhibitors of Lck: synthesis, SAR, and in vivo anti-inflammatory activity.

Amgen
Structure-activity relationships of a novel class of Src SH2 inhibitors.

Ariad Pharmaceuticals
Aminochromane, aminothiochromane and amino-1,2,3,4-tetrahydroquinoline derivatives, pharmaceutical compositions containing them, and their use in therapy

Abbvie Deutschland
Aminotetraline and aminoindane derivatives, pharmaceutical compositions containing them, and their use in therapy

Abbvie Deutschland
Morpholine derivative

Shanghai Pharmaceuticals Holding
6-1H-imidazo-quinazoline and quinolines derivatives, new MAO inhibitors and imidazoline receptor ligands

Rottapharm