16 articles for I Hwang
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
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Article Title
Organization
Optimization of the central heterocycle of alpha-ketoheterocycle inhibitors of fatty acid amide hydrolase.

Institute For Chemical Biology
Optimization of alpha-ketooxazole inhibitors of fatty acid amide hydrolase.

The Scripps Research Institute
Potent and selective alpha-ketoheterocycle-based inhibitors of the anandamide and oleamide catabolizing enzyme, fatty acid amide hydrolase.

The Scripps Research Institute
Discovery of a potent, nonpolyglutamatable inhibitor of glycinamide ribonucleotide transformylase.

The Scripps Research Institute
Discovery of N-benzylbenzamide-based allosteric inhibitors of Aurora kinase A.

Korea Institute of Science and Technology (KIST)
Identification of a novel potent CDK inhibitor degrading cyclinK with a superb activity to reverse trastuzumab-resistance in HER2-positive breast cancer in vivo.

Hanyang University
Discovery of AICAR Tfase inhibitors that disrupt requisite enzyme dimerization.

The Scripps Research Institute
Discovery of a potent, selective, and efficacious class of reversible alpha-ketoheterocycle inhibitors of fatty acid amide hydrolase effective as analgesics.

The Scripps Research Institute
Discovery of an exceptionally potent and selective class of fatty acid amide hydrolase inhibitors enlisting proteome-wide selectivity screening: concurrent optimization of enzyme inhibitor potency and selectivity.

The Scripps Research Institute
Heterocyclic sulfoxide and sulfone inhibitors of fatty acid amide hydrolase.

The Scripps Research Institute
Computational Design of Potent D-Peptide Inhibitors of SARS-CoV-2.

University of Toronto
Design, Synthesis, and Biological Evaluation of New Peripheral 5HT

Gwangju Institute of Science and Technology
Synthesis and anti-renal fibrosis activity of conformationally locked truncated 2-hexynyl-N(6)-substituted-(N)-methanocarba-nucleosides as A3 adenosine receptor antagonists and partial agonists.

Seoul National University
P2X7 modulators

Janssen Pharmaceutica
Substituted bicyclic dihydropyrimidinones and their use as inhibitors of neutrophil elastase activity

Boehringer Ingelheim International
Development and evaluation of a pharmacophore model for inhibitors of aldosterone synthase (CYP11B2).

Saarland University