15 articles for Y Cho
The following articles (labelled with PubMed ID or TBD) are for your review
PMID
Data
Article Title
Organization
Inhibition of veratridine-induced delayed inactivation of the voltage-sensitive sodium channel by synthetic analogs of crambescin B.

Tohoku University
Novel thienopyrimidinones as mGluR1 antagonists.

Yonsei University
The SAR analysis of TRPV1 agonists with thea-methylated B-region.

Seoul National University
N-4-t-Butylbenzyl 2-(4-methylsulfonylaminophenyl) propanamide TRPV1 antagonists: Structure-activity relationships in the A-region.

Seoul National University
2-(4-Methylsulfonylaminophenyl) propanamide TRPV1 antagonists: Structure-activity relationships in the B and C-regions.

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

Ajou University
Norterpene Cyclic Peroxides from the Marine Sponge

Korea Institute of Ocean Science and Technology
Entry inhibition of hepatitis B virus using cyclosporin O derivatives with peptoid side chain incorporation.

Gwangju Insitute of Science and Technology (Gist)
Discovery of G Protein-Biased Ligands against 5-HT

Korea Institute of Science and Technology
Discovery of G Protein-Biased Antagonists against 5-HT

Korea Institute of Science and Technology
Discovery of Novel Pyrimidine-Based Capsid Assembly Modulators as Potent Anti-HBV Agents.

Gwangju Institute of Science and Technology (Gist)
Discovery of (R)-7-cyano-2,3,4, 5-tetrahydro-1-(1H-imidazol-4-ylmethyl)-3- (phenylmethyl)-4-(2-thienylsulfonyl)-1H-1,4-benzodiazepine (BMS-214662), a farnesyltransferase inhibitor with potent preclinical antitumor activity.

Bristol-Myers Squibb Pharmaceutical Research Institute
Discovery and structure-activity relationships of imidazole-containing tetrahydrobenzodiazepine inhibitors of farnesyltransferase.

Bristol-Myers Squibb Pharmaceutical Research Institute
Substituted quinazoline compounds and uses thereof for modulating glucocerebrosidase activity

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

Organon International