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13 articles for J Kong


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

PMID
Cmpds
Data
Article Title
Organization
10
Discovery of PF-5190457, a Potent, Selective, and Orally Bioavailable Ghrelin Receptor Inverse Agonist Clinical Candidate.EBI
Pfizer
27
Identification of potent, selective, CNS-targeted inverse agonists of the ghrelin receptor.EBI
Pfizer
4
Water mediated ligand functional group cooperativity: the contribution of a methyl group to binding affinity is enhanced by a COO(-) group through changes in the structure and thermodynamics of the hydration waters of ligand-thermolysin complexes.EBI
The State University of New York
12
Discovery of a vorapaxar analog with increased aqueous solubility.EBI
Merck Research Laboratories
7
Recent advances in the discovery of protein tyrosine phosphatase SHP2 inhibitors.EBI
Soochow University
20
The synthesis of highly potent, selective, and water-soluble agonists at the human adenosine A3 receptor.EBI
Pfizer
26
Design and optimisation of a small-molecule TLR2/4 antagonist for anti-tumour therapy.EBI
Tsinghua University
7
3'-Aminoadenosine-5'-uronamides: discovery of the first highly selective agonist at the human adenosine A3 receptor.EBI
Pfizer
3
Synthesis and Structure-Activity Relationships of Arylsulfonamides as AIMP2-DX2 Inhibitors for the Development of a Novel Anticancer Therapy.EBI
Dongguk University-Seoul
2
SUBSTITUTED PIPERIDINYL-METHYLPURINE PYRIDINES AND RELATED COMPOUNDS AND THEIR USE IN TREATING DISEASES AND CONDITIONSBDB
K36 Therapeutics
17
P-phenylenediamine derivative as potassium channel regulator and preparation method and medical application thereofBDB
Shanghai Zhimeng Biopharma
47
Heterocyclic derivatives and their use in the treatment of neurological disordersBDB
Novartis
25
Dual-site binding of bivalent 4-aminopyridine- and 4-aminoquinoline-based AChE inhibitors: contribution of the hydrophobic alkylene tether to monomer and dimer affinities.BDB
Hong Kong University of Science and Technology