Structure–activity relationships of trans-substituted-propenoic acid derivatives on the nicotinic acid receptor HCA2 (GPR109A)-Reference-Cited by-同舟云学术

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Structure–activity relationships of trans-substituted-propenoic acid derivatives on the nicotinic acid receptor HCA2 (GPR109A)

Published:2011-05 Issue:9 Volume:21 Page:2736-2739
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

van Veldhoven J.P.D.,Blad C.C.,Artsen C.M.,Klopman C.,Wolfram D.R.,Abdelkadir M.J.,Lane J.R.,Brussee J.,IJzerman A.P.

Publisher

Elsevier BV

Subject

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

Reference22 articles.

1. One-year reduction and longitudinal analysis of carotid intima-media thickness associated with colestipol/niacin therapy.

2. Molecular identification of nicotinic acid receptor

3. PUMA-G and HM74 are receptors for nicotinic acid and mediate its anti-lipolytic effect

4. Molecular Identification of High and Low Affinity Receptors for Nicotinic Acid

5. Offermanns, S.; Colleti, S. L.; Lovenberg, T. W.; Semple, G.; Wise, A.; IJzerman, A. P. Pharmacol. Rev., in press.

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