Abstract
Several potent, functionally active MCHr1 antagonists derived from quinolin-2(1H)-ones and quinazoline-2(1H)-ones have been synthesized and evaluated. Pyridylmethyl substitution at the quinolone 1-position results in derivatives with low-nM binding potency and good selectivity with respect to hERG binding.
MeSH terms
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Animals
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Mice
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Quinazolines / chemistry*
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Quinazolines / pharmacokinetics
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Quinazolines / pharmacology*
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Quinolones / chemistry*
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Quinolones / pharmacokinetics
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Quinolones / pharmacology*
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Receptors, Pituitary Hormone / antagonists & inhibitors*
Substances
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Quinazolines
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Quinolones
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Receptors, Pituitary Hormone
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melanin-concentrating hormone receptor