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tandospirone

Known as: 3a,4,7,7a-hexahydro-2-(4-(4-(2-pyrimidinyl)-1-piperazinyl)butyl)-4,7-methano-1H-isoindole-1,3(2H)-dione, (1R*,2S*,3R*,4S*)-N-(4-(4-(2-Pyrimidinyl)-1-Piperazinyl)Butyl)-2,3-Norbornanedicarboximide, 4,7-Methano-1H-Isoindole-1,3(2h)-Dione, Hexahydro-2-(4-(4-(2-Pyrimidinyl)-1-Piperazinyl)Butyl)-, (3a-Alpha,4Beta,7Beta,7a-Alpha)- 
 
National Institutes of Health

Papers overview

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2015
2015
PURPOSE To determine the safety and efficacy of AL-8309B (tandospirone) in the management of patients with geographic atrophy (GA… Expand
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Review
2013
Review
2013
The N-methyl-D-aspartate receptor (NMDAR) antagonists, phencyclidine (PCP), dizocilpine (MK-801), or ketamine, given… Expand
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2009
2009
We studied the effects of tandospirone, a 5-HT(1A) agonistic anxiolytic agent, on haloperidol-induced catalepsy and forebrain Fos… Expand
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Review
2008
Review
2008
Cognitive impairment is a key feature of schizophrenia and may be the most important determinant of outcome in schizophrenia… Expand
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Highly Cited
2005
Highly Cited
2005
This study examined the abilities of 5-hydroxytryptamine (5-HT) agonists with varying selectivity for different subtypes of 5-HT… Expand
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Highly Cited
2001
Highly Cited
2001
OBJECTIVE The goal of this study was to evaluate the effects of the addition of tandospirone, a serotonin-1A (5-HT(1A)) agonist… Expand
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Highly Cited
2001
Highly Cited
2001
BACKGROUND The purpose of this study was to test the hypothesis that the addition of tandospirone, a 5-HT(1A) partial agonist, to… Expand
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2001
2001
Abstract: Flumioxazin and sulfentrazone were compared for phytotoxicity on 15 soybean varieties in a greenhouse study and four… Expand
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1993
1993
The effects of acute and chronic treatment of rats with the tricyclic antidepressant imipramine, the 5-HT1A receptor partial… Expand
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Highly Cited
1993
Highly Cited
1993
A putative animal model of anxiety based on shock-induced ultrasonic vocalization was pharmacologically validated in young adult… Expand
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