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(1aR,5aR)1a,3,5,5a-Tetrahydro-1H-2,3-diaza-cyclopropa[a]pentalene-4-carboxylic Acid (MK-1903): A Potent GPR109aAgonist that Lowers Free Fatty Acids in Humans.

Authors :
Boatman, P. Douglas
Lauring, Brett
Schrader, Thomas O.
Kasem, Michelle
Johnson, Benjamin R.
Skinner, Philip
Jung, Jae-Kyu
Xu, Jerry
Cherrier, Martin C.
Webb, Peter J.
Semple, Graeme
Sage, Carleton R.
Knudsen, Jens
Chen, Ruoping
Luo, Wen-Lin
Caro, Luzelena
Cote, Josee
Lai, Eseng
Wagner, John
Taggart, Andrew K.
Source :
Journal of Medicinal Chemistry. Apr2012, Vol. 55 Issue 8, p3644-3666. 23p.
Publication Year :
2012

Abstract

G-protein coupled receptor (GPCR) GPR109a is a moleculartarget for nicotinic acid and is expressed in adipocytes, spleen,and immune cells. Nicotinic acid has long been used for the treatmentof dyslipidemia due to its capacity to positively affect serum lipidsto a greater extent than other currently marketed drugs. We reporta series of tricyclic pyrazole carboxylic acids that are potent andselective agonists of GPR109a. Compound R,R-19a(MK-1903) was advanced through preclinicalstudies, was well tolerated, and presented no apparent safety concerns.Compound R,R-19awasadvanced into a phase 1 clinical trial and produced a robust decreasein plasma free fatty acids. On the basis of these results, R,R-19awas evaluated in aphase 2 study in humans. Because R,R-19aproduced only a weak effect on serum lipids ascompared with niacin, we conclude that the beneficial effects of niacinare most likely the result of an undefined GPR109a independent pathway. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00222623
Volume :
55
Issue :
8
Database :
Academic Search Index
Journal :
Journal of Medicinal Chemistry
Publication Type :
Academic Journal
Accession number :
74758352
Full Text :
https://doi.org/10.1021/jm2010964