19 articles for J Hawkins
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Synthesis and muscarinic activities of quinuclidin-3-yltriazole and -tetrazole derivatives.

Smithkline Beecham Pharmaceuticals
Substituent variation in azabicyclic triazole- and tetrazole-based muscarinic receptor ligands.

Smithkline Beecham Pharmaceuticals
Discovery of imidazo[1,5-a]pyridines and -pyrimidines as potent and selective RORc inverse agonists.

Genentech
A reversed sulfonamide series of selective RORc inverse agonists.

Argenta Discovery
Identification of tertiary sulfonamides as RORc inverse agonists.

Genentech
Diverse heterocyclic scaffolds as allosteric inhibitors of AKT.

Astrazeneca
BACE-1 hydroxyethylamine inhibitors using novel edge-to-face interaction with Arg-296.

Glaxosmithkline
BACE-1 inhibitors part 1: identification of novel hydroxy ethylamines (HEAs).

Glaxosmithkline
BACE-1 inhibitors part 2: identification of hydroxy ethylamines (HEAs) with reduced peptidic character.

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

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

Astrazeneca
Design of [R-(Z)]-(+)-alpha-(methoxyimino)-1-azabicyclo[2.2.2]octane-3-acetonitri le (SB 202026), a functionally selective azabicyclic muscarinic M1 agonist incorporating the N-methoxy imidoyl nitrile group as a novel ester bioisostere.

Smithkline Beecham Pharmaceuticals
Pyridine-derived γ-secretase modulators.

Glaxosmithkline Pharmaceuticals
Treatment of infectious diseases with glucose uptake inhibitors

Kadmon
Inhibiting agents for Bruton's tyrosine kinase

Biogen Ma
Factor IXa inhibitors

Merck Sharp & Dohme
N-substituted pyrazolo [3,4-D] pyrimidine ketone compound, and preparation process and use thereof

Sun Yat-Sen University
Rho kinase inhibitors and methods of use

H. Lee Moffitt Cancer Center and Research Institute
Discovery and preclinical profile of Saxagliptin (BMS-477118): a highly potent, long-acting, orally active dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes.

Bristol-Myers Squibb Pharmaceutical Research Institute