16 articles for HJ Jung
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
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Article Title
Organization
Replacing the terminal piperidine in ceritinib with aliphatic amines confers activities against crizotinib-resistant mutants including G1202R.

Korea Research Institute of Chemical Technology
Development of a novel class of mitochondrial ubiquinol-cytochrome c reductase binding protein (UQCRB) modulators as promising antiangiogenic leads.

Yonsei University
Design, synthesis, and anti-melanogenic efficacy of 2-mercaptobenzoxazoles with nanomolar tyrosinase activity inhibition.

Pusan National University
In vitro and in vivo anti-pigmentation effects of 2-mercaptobenzimidazoles as nanomolar tyrosinase inhibitors on mammalian cells and zebrafish embryos: Preparation of pigment-free zebrafish embryos.

Pusan National University
Discovery of novel tetrahydroisoquinoline-containing pyrimidines as ALK inhibitors.

Korea Research Institute of Chemical Technology
Identification of BR102910 as a selective fibroblast activation protein (FAP) inhibitor.

Sungkyunkwan University
Identification of BR101549 as a lead candidate of non-TZD PPARγ agonist for the treatment of type 2 diabetes: Proof-of-concept evaluation and SAR.

Boryung Pharmaceuticals
Discovery of the bifunctional modulator of angiotensin II type 1 receptor (AT1R) and PPARγ derived from the AT1R antagonist, Fimasartan.

Boryung Pharmaceuticals
Ethynyl derivatives

Hoffmann-La Roche
Alkylphenyl compounds

Bristol-Myers Squibb
Identification of conformationally sensitive residues essential for inhibition of vesicular monoamine transport by the noncompetitive inhibitor tetrabenazine.

Hebrew University of Jerusalem
Multiheteroaryl compounds as inhibitors of H-PGDS and their use for treating prostaglandin D2 mediated diseases

Cayman Chemical
Bcl-2-selective apoptosis-inducing agents for the treatment of cancer and immune diseases

Abbvie
Bicyclic aryl and heteroaryl sodium channel inhibitors

Amgen
TRPV1 antagonists

TBA