BindingDB

The first public molecular recognition database, BindingDB supports research, education and practice in drug discovery, pharmacology and related fields.

BindingDB contains 3.2M data for 1.4M Compounds and 11.4K Targets. Of those, 1.6M data for 756K Compounds and 4.8K Targets were curated by BindingDB curators. BindingDB is a FAIRsharing resource.

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29 articles for H Rhim

The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Data
Article Title
Organization
5-HT7 receptor modulators: Amino groups attached to biphenyl scaffold determine functional activity.EBI
Yonsei University
Novel N-acyl-carbazole derivatives as 5-HT7R antagonists.EBI
Yonsei University
3-Benzamides and 3,4,5-trimethoxyphenyl amines as calcium channel blockers.EBI
Ewha Womans University
Synthesis and biological evaluation of isoxazoline derivatives as potent M1 muscarinic acetylcholine receptor agonists.EBI
Korea Institute of Science and Technology
Synthesis and biological evaluation of 4-nitroindole derivatives as 5-HT2A receptor antagonists.EBI
Ewha Womans University
Novel N-biphenyl-2-ylmethyl 2-methoxyphenylpiperazinylalkanamides as 5-HT7R antagonists for the treatment of depression.EBI
Yonsei University
Discovery of aryl-biphenyl-2-ylmethylpiperazines as novel scaffolds for 5-HT(7) ligands and role of the aromatic substituents in binding to the target receptor.EBI
Institute of Science and Technology
Synthesis and biological evaluation of benzoisothiazole derivatives possessing N,N-dimethylformimidamide group as 5-HT6 receptor antagonists.EBI
Ewha Womans University
Synthesis and biological evaluation of oxazole derivatives as T-type calcium channel blockers.EBI
Institute of Science and Technology
Quinazolindione derivatives as potent 5-HT3A receptor antagonists.EBI
Konkuk University
Design, synthesis, and biological evaluation of 1,3-dioxoisoindoline-5-carboxamide derivatives as T-type calcium channel blockers.EBI
Institute of Science and Technology
Synthesis and biological activity of 3,4-dihydroquinazolines for selective T-type Ca2+ channel blockers.EBI
Korea Institute of Science & Technology
Synthesis and T-type calcium channel blocking activity of novel diphenylpiperazine compounds, and evaluation of in vivo analgesic activity.EBI
Ewha Womans University
Synthesis and biological evaluation of 1,4-diazepane derivatives as T-type calcium channel blockers.EBI
Institute of Science and Technology
Synthesis and biological evaluation of (phenylpiperazinyl-propyl)arylsulfonamides as selective 5-HT(2A) receptor antagonists.EBI
Ewha Womans University
Synthesis and evaluation of alpha,alpha'-disubstituted phenylacetate derivatives for T-type calcium channel blockers.EBI
Institute of Science and Technology
T-type Ca2+ channel blockers suppress the growth of human cancer cells.EBI
Kyung Hee University
Preparation of piperazine derivatives as 5-HT7 receptor antagonists.EBI
Ewha Womans University
Discovery of potent T-type calcium channel blocker.EBI
Kyung Hee University
Lead discovery and optimization of T-type calcium channel blockers.EBI
Institute of Science and Technology
3D pharmacophore based virtual screening of T-type calcium channel blockers.EBI
Institute of Science and Technology
Synthesis and biological evaluation of novel T-type calcium channel blockers.EBI
Kyung Hee University
Novel T-type calcium channel blockers: dioxoquinazoline carboxamide derivatives.EBI
Institute of Science and Technology
Morpholin-2-one derivatives as novel selective T-type Ca2+ channel blockers.EBI
Institute of Science and Technology
3,4-Dihydroquinazoline derivatives as novel selective T-type Ca2+ channel blockers.EBI
Institute of Science & Technology
In vitro cytotoxicity on human ovarian cancer cells by T-type calcium channel blockers.EBI
Kyung Hee University
Design and synthesis of novel series of 5-HT6 receptor ligands having indole, a central aromatic core and 1-amino-4 methyl piperazine as a positive ionizable group.EBI
Ewha Womans University
Synthesis and the 5-HT6 receptor antagonistic effect of 3-arylsulfonylamino-5,6-dihydro-6-substituted pyrazolo[3,4]pyridinones for neuropathic pain treatment.EBI
Korea Institute of Science & Technology (Kist)
Discovery of β-Arrestin Biased Ligands of 5-HTEBI
Korea Institute of Science and Technology