Naphthol derivatives as TRPV1 inhibitors for the treatment of urinary incontinence-Reference-Cited by-同舟云学术

Naphthol derivatives as TRPV1 inhibitors for the treatment of urinary incontinence

Published:2011-06 Issue:11 Volume:21 Page:3354-3357
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Urbahns Klaus,Yura Takeshi,Mogi Muneto,Tajimi Masaomi,Fujishima Hiroshi,Masuda Tsutomu,Yoshida Nagahiro,Moriwaki Toshiya,Lowinger Timothy B.,Meier Heinrich,Chan Fiona,Madge David,Gupta Jang B.

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference15 articles.

1. The vanilloid receptor TRPV1: 10 years from channel cloning to antagonist proof-of-concept

2. Analgesic potential of TRPV1 antagonists

3. Clinical development of TRPV1 antagonists: targeting a pivotal point in the pain pathway

4. Setbacks in the Clinical Development of TRPV1 Antagonists: What Next?

5. The paradoxical role of the transient receptor potential vanilloid 1 receptor in inflammation

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4. Electroacupuncture protects against bladder dysfunction induced by acute urinary retention via TRPV1/ATP signaling pathway: An animal and human research study;Biochemical and Biophysical Research Communications;2022-10

5. 2-Naphthol-pyrazole conjugates as substrates in the Mannich reaction;Zeitschrift für Naturforschung B;2018-03-20