15 articles for M Kang
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Oxaspirol B with p97 Inhibitory Activity and Other Oxaspirols from Lecythophora sp. FL1375 and FL1031, Endolichenic Fungi Inhabiting Parmotrema tinctorum and Cladonia evansii.

University of Arizona
Efficacious and orally bioavailable thrombin inhibitors based on a 2,5-thienylamidine at the P1 position: discovery of N-carboxymethyl-d-diphenylalanyl-l-prolyl[(5-amidino-2-thienyl)methyl]amide.

Lg Life Sciences
Novel thiophenyl C-aryl glucoside SGLT2 inhibitors as potential antidiabetic agents.

Green Cross
Forward chemical genetic approach identifies new role for GAPDH in insulin signaling.

New York University
Discovery of novel amidobenzimidazole derivatives as orally available small molecule modulators of stimulator of interferon genes for cancer immunotherapy.

Korea Research Institute of Chemical Technology
Discovery of thiophen-2-ylmethylene bis-dimedone derivatives as novel WRN inhibitors for treating cancers with microsatellite instability.

Korea University
Discovery of Orally Bioavailable Phthalazinone Analogues as an ENPP1 Inhibitor for STING-Mediated Cancer Immunotherapy.

Ajou University
Development of Potent Immune Modulators Targeting Stimulator of Interferon Genes Receptor.

Korea Research Institute of Chemical Technology
Discovery of GCC5694A: A potent and selective sodium glucose co-transporter 2 inhibitor for the treatment of type 2 diabetes.

Gc Pharma
Discovery of N-amido-phenylsulfonamide derivatives as novel microsomal prostaglandin E

Kyung Hee University
N-(3-acyloxy-2-benzylpropyl)-N'-[4-(methylsulfonylamino)benzyl]thiourea analogues: novel potent and high affinity antagonists and partial antagonists of the vanilloid receptor.

Seoul National University
Noncovalent thrombin inhibitors incorporating an imidazolylethynyl P1.

Lg Chemical
Spirohexenolide A targets human macrophage migration inhibitory factor (hMIF).

University of California-San Diego
Inactivation of a novel neuropeptide Y/peptide YY receptor gene in primate species.

Yamanouchi Pharmaceutical
Neurochemical and autonomic pharmacological profiles of the 6-aza-analogue of mianserin, Org 3770 and its enantiomers.

Organon International