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Andrew J Grottick
Author PubWeight™ 14.36
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Top papers
Rank
Title
Journal
Year
PubWeight™
‹?›
1
Lorcaserin, a novel selective human 5-hydroxytryptamine2C agonist: in vitro and in vivo pharmacological characterization.
J Pharmacol Exp Ther
2008
2.17
2
Differential effects of the 5-HT(2A) receptor antagonist M100907 and the 5-HT(2C) receptor antagonist SB242084 on cocaine-induced locomotor activity, cocaine self-administration and cocaine-induced reinstatement of responding.
Neuropsychopharmacology
2002
1.49
3
Discovery and structure-activity relationship of (1R)-8-chloro-2,3,4,5-tetrahydro-1-methyl-1H-3-benzazepine (Lorcaserin), a selective serotonin 5-HT2C receptor agonist for the treatment of obesity.
J Med Chem
2007
1.27
4
Discovery of the first potent and orally efficacious agonist of the orphan G-protein coupled receptor 119.
J Med Chem
2008
1.16
5
Anxiolytic- and antidepressant-like profile of ATC0065 and ATC0175: nonpeptidic and orally active melanin-concentrating hormone receptor 1 antagonists.
J Pharmacol Exp Ther
2005
1.01
6
A new family of H3 receptor antagonists based on the natural product Conessine.
Bioorg Med Chem Lett
2007
0.96
7
Phencyclidine exacerbates attentional deficits in a neurodevelopmental rat model of schizophrenia.
Neuropsychopharmacology
2003
0.89
8
The potential use of selective 5-HT2C agonists in treating obesity.
Expert Opin Investig Drugs
2006
0.88
9
Discovery of fused bicyclic agonists of the orphan G-protein coupled receptor GPR119 with in vivo activity in rodent models of glucose control.
Bioorg Med Chem Lett
2011
0.84
10
Design and evaluation of novel biphenyl sulfonamide derivatives with potent histamine H(3) receptor inverse agonist activity.
J Med Chem
2009
0.81
11
Nelotanserin, a novel selective human 5-hydroxytryptamine2A inverse agonist for the treatment of insomnia.
J Pharmacol Exp Ther
2009
0.79
12
Discovery of a second generation agonist of the orphan G-protein coupled receptor GPR119 with an improved profile.
Bioorg Med Chem Lett
2011
0.78
13
Diet-induced models of obesity (DIO) in rodents.
Curr Protoc Neurosci
2012
0.77
14
Pyrimidine-based antagonists of h-MCH-R1 derived from ATC0175: in vitro profiling and in vivo evaluation.
Bioorg Med Chem Lett
2009
0.76
15
Identification of biaryl sulfone derivatives as antagonists of the histamine H₃ receptor: discovery of (R)-1-(2-(4'-(3-methoxypropylsulfonyl)biphenyl-4-yl)ethyl)-2-methylpyrrolidine (APD916).
Bioorg Med Chem Lett
2011
0.75
16
Novel H3 receptor antagonists with improved pharmacokinetic profiles.
Bioorg Med Chem Lett
2008
0.75
17
Identification of fused bicyclic heterocycles as potent and selective 5-HT(2A) receptor antagonists for the treatment of insomnia.
Bioorg Med Chem Lett
2012
0.75
18
Synthesis and in vivo evaluation of phenethylpiperazine amides: selective 5-hydroxytryptamine(2A) receptor antagonists for the treatment of insomnia.
J Med Chem
2010
0.75