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S 14506

Known as: S-14506 
 
National Institutes of Health

Papers overview

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2013
2013
Poisoning by organophosphate nerve agents can induce seizures which rapidly become refractory to treatment and result in brain… Expand
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2005
2005
SummaryThe tritiated derivative of the potent 5-HT1A receptor agonist S-14506 {1[2-(4-fluorobenzoylamino)ethyl]-4-(7… Expand
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2005
2005
Apomorphine and mCPP induced yawning associated with penile erections in rats, whereas physostigmine induced only yawns… Expand
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2001
2001
S 14506 is chemically related to the inverse agonist at 5-HT(1A) receptors, spiperone, but S 14506 behaves as one of the most… Expand
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2000
2000
Abstract Rationale: Maximal responses are often used as a measure of intrinsic activity or efficacy, but cannot be directly… Expand
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1999
1999
G protein-coupled receptors exist in G protein-coupled and -uncoupled forms that exhibit high and low affinity for agonists… Expand
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1998
1998
The interoceptive stimulus induced by clozapine (5 mg/kg, i.p.) has been characterized in an operant drug discrimination… Expand
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1994
1994
S 14506 (1-[-(4-fluorobenzoylamino)ethyl]-4-(7-methoxynaphthyl)piper azine hydrochloride), 8-OH-DPAT ((+/-)-8… Expand
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1994
1994
The high efficacy methoxynaphtylpiperazine 5-HT1A receptor agonists, S 14506 (1-[2-(4-fluorobenzoylamino)ethyl]-4-(7… Expand
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1994
1994
This study assessed the dependence potential of S-14506 [ 1- [ 2-(4-fluorobenzoylamino)ethyl]-4-(7-methoxy napthyl) piperazine… Expand
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