PMID

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Article Title

Organization

Development of substituted N-[3-(3-methoxylphenyl)propyl] amides as MT(2)-selective melatonin agonists: improving metabolic stability.

Hong Kong University of Science and Technology

Potent, easily synthesized huperzine A-tacrine hybrid acetylcholinesterase inhibitors.

Hong Kong University of Science and Technology

Synthesis of a potent wide-spectrum serotonin-, norepinephrine-, dopamine-reuptake inhibitor (SNDRI) and a species-selective dopamine-reuptake inhibitor based on the gamma-amino alcohol functional group.

Hong Kong University of Science and Technology

Synthesis of substituted N-[3-(3-methoxyphenyl)propyl] amides as highly potent MT(2)-selective melatonin ligands.

Hong Kong University of Science and Technology

Compounds for use in methods for treating diseases or conditions mediated by protein disulfide isomerase

Beth Israel Deaconess Medical Center

3-substituted 2-amino-indole derivatives

Takeda Pharmaceutical

Structure-based design, synthesis, and biological evaluation of conformationally restricted novel 2-alkylthio-6-[1-(2,6-difluorophenyl)alkyl]-3,4-dihydro-5-alkylpyrimidin-4(3H)-ones as non-nucleoside inhibitors of HIV-1 reverse transcriptase.

Sapienza University of Rome