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S003

Sigma-Aldrich

1-(1-Naphthyl)piperazine hydrochloride

needles

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About This Item

Fórmula empírica (Notação de Hill):
C14H16N2 · HCl
Peso molecular:
248.75
Número MDL:
MFCD00055161
Código UNSPSC:
12352200
ID de substância PubChem:
24278118

forma

needles

cor

white

solubilidade

H2O: soluble
ethanol: slightly soluble

cadeia de caracteres SMILES

Cl.C1CN(CCN1)c2cccc3ccccc23

InChI

1S/C14H16N2.ClH/c1-2-6-13-12(4-1)5-3-7-14(13)16-10-8-15-9-11-16;/h1-7,15H,8-11H2;1H

chave InChI

ZYVYPNZFOCZLEM-UHFFFAOYSA-N

Informações sobre genes

human ... HTR1A(3350) , HTR1B(3351) , HTR1D(3352) , HTR1E(3354) , HTR1F(3355) , HTR2A(3356) , HTR2B(3357) , HTR2C(3358)

Ações bioquímicas/fisiológicas

5-HT1 serotonin receptor agonist; 5-HT2 serotonin receptor antagonist.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

Certificados de análise (COA)

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M S Herness et al.
The Journal of membrane biology, 173(2), 127-138 (2000-01-12)
Recently we reported that rat taste receptor cells respond to the neurotransmitter serotonin with an inhibition of a calcium-activated potassium current [17]. In the present study, this observation is confirmed and extended by studying the effects of an array of
P J Pauwels et al.
British journal of pharmacology, 123(1), 51-62 (1998-03-04)
1. The guinea-pig recombinant 5-hydroxytryptamine1B (gp 5-HT1B) receptor stably transfected in rat C6-glial cells was characterized by monitoring G-protein activation in a membrane preparation with agonist-stimulated [35S]-GTPgammaS binding. The intrinsic activity of 5-HT receptor ligands was compared with that determined
R W Fuller et al.
Research communications in chemical pathology and pharmacology, 51(1), 37-45 (1986-01-01)
1-(1-Naphthyl)piperazine (1-NP) had high affinity for tritiated serotonin, tritiated LSD (lysergic acid diethylamide) and tritiated spiperone binding sites in rat brain cortex in vitro. 1-NP at doses of 3-30 mg/kg i.p. decreased 5-hydroxyindoleacetic acid (5-HIAA) concentration in whole brain of
E Béjar et al.
The Journal of pharmacy and pharmacology, 47(8), 637-642 (1995-08-01)
Biphasic cumulative concentration-response curves to 5-hydroxytryptamine (5-HT) and alpha-methyl-5-hydroxytryptamine (alpha-Me-5-HT) using rat stomach fundus in the presence of 50 microM pargyline suggested two sites of interaction (high and low affinity). The order of agonist potencies of 5-HT agonists for the

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