20 articles for J Kang
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Cmpds
Data
Article Title
Organization
40
Discovery of a First-in-Class Receptor Interacting Protein 1 (RIP1) Kinase Specific Clinical Candidate (GSK2982772) for the Treatment of Inflammatory Diseases.

Queen Mary University of London
15
DNA-Encoded Library Screening Identifies Benzo[b][1,4]oxazepin-4-ones as Highly Potent and Monoselective Receptor Interacting Protein 1 Kinase Inhibitors.

Glaxosmithkline
4
Crystal structures of human RIP2 kinase catalytic domain complexed with ATP-competitive inhibitors: Foundations for understanding inhibitor selectivity.

Glaxosmithkline
17
Synthesis and biological evaluation of 1-(2-hydroxy-3-phenyloxypropyl)piperazine derivatives as T-type calcium channel blockers.

Korea Institute of Science and Technology
51
Novel C-aryl glucoside SGLT2 inhibitors as potential antidiabetic agents: 1,3,4-Thiadiazolylmethylphenyl glucoside congeners.

Green Cross
32
Characterization of HERG potassium channel inhibition using CoMSiA 3D QSAR and homology modeling approaches.

Aventis Pharmaceuticals
2
Aß-tryptase inhibitor with a tropanylamide scaffold to improve in vitro stability and to lower hERG channel binding affinity.

Sanofi Pharmaceuticals
37
Synthesis and SAR of sulfoxide substituted carboxyquinolines as NK3 receptor antagonists.

AstraZeneca
42
4-aryl piperazine and piperidine amides as novel mGluR5 positive allosteric modulators.

AstraZeneca
31
Synthesis and biological evaluation of 3-aminopyrrolidine derivatives as CC chemokine receptor 2 antagonists.

Yang Ji Chemical Co.
59
Substituted pyrimidines as cannabinoid CB1 receptor ligands.

Green Cross
8
Identification of Thieno[3,2-d]pyrimidine derivatives as potent and selective Janus Kinase 1 inhibitors.

Korea University
20
Structurally Minimalized and Druglike TGase2 Inhibitors Based on 7-Aminoquinoline-5,8-dione Scaffolds for the Treatment of Diabetic Retinopathy.

Daegu-Gyeongbuk Medical Innovation Foundation
25
Targeting Solvent-Front Mutations for Kinase Drug Discovery: From Structural Basis to Design Strategies.

Jinan University
29
Lead discovery and optimization of T-type calcium channel blockers.

Institute of Science and Technology
5
Design of bivalent ligands using hydrogen bond linkers: synthesis and evaluation of inhibitors for human beta-tryptase.

Aventis Pharmaceuticals
8
Identification of a RIP1 Kinase Inhibitor Clinical Candidate (GSK3145095) for the Treatment of Pancreatic Cancer.

Glaxosmithkline
2
Discovery of thienothiazolocarboxamide analogues as novel anti-tubercular agent.

Institut Pasteur Korea
11
FXR (NR1H4) modulating compounds

Gilead Sciences
39
Substituted aminopyrimidine compounds and methods of use

Calitor Sciences