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- W2045593417 abstract "A series of new pyridine hydrazide derivatives with high and selective antagonist activity at the human neuropeptide Y Y 5 receptor were developed. Introduction of electron-withdrawing groups into the arylsulfonamide rest, together with the 3-pyridyl analogue in the hydrazide moiety, led to a significant improvement of potency and solubility, affording trans-N-{4-[N'-(pyridine-3-carbonyl)hydrazino-carbonyl]cyclohexylmethyl}-2,4-dichloro-benzenesulfonamide (14), which binds to the hY 5 receptor with an IC 50 value of 7.44 nmol/L." @default.
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- W2045593417 date "2005-06-14" @default.
- W2045593417 modified "2023-09-25" @default.
- W2045593417 title "Novel Human Neuropeptide Y Y5 Receptor Antagonists for the Treatment of Obesity. Synthesis and Biological Evaluation of Pyridine Hydrazide Derivatives." @default.
- W2045593417 doi "https://doi.org/10.1002/chin.200524215" @default.
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