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Jose L Mendez-Andino

Explore the profile of Jose L Mendez-Andino including associated specialties, affiliations and a list of published articles. Areas
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Articles 6
Citations 25
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Recent Articles
1.
Mendez-Andino J, Wos J
Drug Discov Today . 2007 Nov; 12(21-22):972-9. PMID: 17993417
Despite the high number of drug-discovery programs dedicated to finding small-molecule MCH-R1 antagonists for the treatment of obesity and/or mood disorders, a very limited number of these have progressed into...
2.
Mendez-Andino J, Colson A, Meyers K, Mitchell M, Hodge K, Howard J, et al.
Bioorg Med Chem . 2007 Jan; 15(5):2092-105. PMID: 17236777
The design, synthesis, and biological studies of a novel class of MCH-R1 antagonists based on an aminotetrahydronaphthalene ketopiperazine scaffold is described. Compounds within this class promoted significant body weight reduction...
3.
Meyers K, Mendez-Andino J, Colson A, Warshakoon N, Wos J, Mitchell M, et al.
Bioorg Med Chem Lett . 2006 Nov; 17(3):819-22. PMID: 17107796
A direct correlation between hERG binding and QTc prolongation was established for a series of aminomethyl tetrahydronaphthalene ketopiperazine MCH-R1 antagonists. Compounds within this class with greater selectivity over hERG were...
4.
Meyers K, Kim N, Mendez-Andino J, Eric Hu X, Mumin R, Klopfenstein S, et al.
Bioorg Med Chem Lett . 2006 Nov; 17(3):814-8. PMID: 17107791
Aminomethyl tetrahydronaphthalene biphenyl carboxamide MCH-R1 antagonists with greater selectivity over hERG were identified. SAR studies addressing two distinct alternatives for structural modifications leading to improve hERG selectivity are described.
5.
Kim N, Meyers K, Mendez-Andino J, Warshakoon N, Ji W, Wos J, et al.
Bioorg Med Chem Lett . 2006 Aug; 16(20):5445-50. PMID: 16879961
A substituted 4-aminopiperidine was identified as showing activity in an MCH assay from an HTS effort. Subsequent structural modification of the scaffold led to the identification of a number of...
6.
Warshakoon N, Sheville J, Bhatt R, Ji W, Mendez-Andino J, Meyers K, et al.
Bioorg Med Chem Lett . 2006 Jul; 16(19):5207-11. PMID: 16870427
A novel series of substituted quinoline analogs were designed and synthesized as potent and selective melanin concentrating hormone (MCH) antagonists. These analogs show potent (nM) activity (12a-k) with a moderate...