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Updated: May 23, 2026

Yeast Luminometric and Xenopus Oocyte Electrophysiological Examinations of the Molecular Mechanosensitivity of TRPV4
Published on: December 31, 2013
Tetrahydro-naphthols as orally available TRPV1 inhibitors
Klaus Urbahns1, Takeshi Yura, Jang B Gupta
1Research Center Kyoto, Bayer Yakuhin, Ltd, Kizu, Soraku, Kyoto, Japan. Klaus.Urbahns@merckgroup.com
Abstract:
Starting from a naphthol-based lead series with low oral bioavailability, we have identified potent TRPV1 antagonists with oral bioavailability in rats. These compounds emerged from SAR studies aimed at replacing the lead's phenol structure whilst maintaining potency. Compound rac-6a is an orally available TRPV1 antagonist with single-digit nanomolar activity. The enantiomers show a low eudismic ratio at the receptor level.
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