PMID

Data

Article Title

Organization

Modulation by drugs of human hepatic sodium-dependent bile acid transporter (sodium taurocholate cotransporting polypeptide) activity.

Vanderbilt University School of Medicine

Bile acid conjugates of a nonsteroidal glucocorticoid receptor modulator.

Abbott Laboratories

Recent advances in steroid amino acid conjugates: Old scaffolds with new dimensions.

Panjab University

Discovery and Optimization of Biaryl Alkyl Ethers as a Novel Class of Highly Selective, CNS-Penetrable, and Orally Active Adaptor Protein-2-Associated Kinase 1 (AAK1) Inhibitors for the Potential Treatment of Neuropathic Pain.

Bristol-Myers Squibb

Inhibiting Sodium Taurocholate Cotransporting Polypeptide in HBV-Related Diseases: From Biological Function to Therapeutic Potential.

Southwest Jiaotong University

Synthesis and biological evaluation of novel steroidal pyrazoles as substrates for bile acid transporters.

Xenoport

Discovery of (

Bristol-Myers Squibb

Design of Dimeric Bile Acid Derivatives as Potent and Selective Human NTCP Inhibitors.

National Institute of Biological Sciences

Potent and Specific Inhibition of NTCP-Mediated HBV/HDV Infection and Substrate Transporting by a Novel, Oral-Available Cyclosporine A Analogue.

National Institute of Biological Sciences

Design, synthesis and biological evaluation of benzamide derivatives as novel NTCP inhibitors that induce apoptosis in HepG2 cells.

Southwest Jiaotong University

(Hetero)aryl cyclopropylamine compounds as LSD1 inhibitors

Oryzon Genomics

Pyrazolopyrimidines as metabotropic glutamate 5 receptor antagonists

Boehringer Ingelheim International