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Q1004

Sigma-Aldrich

Quipazine maleate salt

Quipazine maleate salt

Synonym(s):

2-(1-Piperazinyl)quinoline maleate salt

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50 MG
$118.00
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$452.00

$118.00

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50 MG
$118.00
250 MG
$452.00

About This Item

Empirical Formula (Hill Notation):
C13H15N3 · C4H4O4
CAS Number:
5786-68-5
Molecular Weight:
329.35
EC Number:
227-314-2
MDL number:
MFCD00133796
UNSPSC Code:
12352200
PubChem Substance ID:
24278122
NACRES:
NA.77

$118.00

Available to ship onMay 01, 2025Details

Request a Bulk Order

solubility

H2O: soluble
alcohol: soluble
dilute aqueous acid: soluble

Quality Level

200

storage temp.

2-8°C

SMILES string

OC(=O)\C=C/C(O)=O.C1CN(CCN1)c2ccc3ccccc3n2

InChI

1S/C13H15N3.C4H4O4/c1-2-4-12-11(3-1)5-6-13(15-12)16-9-7-14-8-10-16;5-3(6)1-2-4(7)8/h1-6,14H,7-10H2;1-2H,(H,5,6)(H,7,8)/b;2-1-

InChI key

QYJJDHZHSCTBII-BTJKTKAUSA-N

Gene Information

human ... HTR1A(3350) , HTR1B(3351) , HTR1D(3352) , HTR1E(3354) , HTR1F(3355) , HTR2A(3356) , HTR2B(3357) , HTR2C(3358) , HTR3A(3359) , HTR3B(9177) , HTR3C(170572) , HTR3D(200909) , HTR3E(285242) , HTR4(3360) , HTR5A(3361) , HTR5B(645694) , HTR6(3362) , HTR7(3363)

Application

Quipazine maleate salt has been used as a serotonin receptor agonist to study its effects on mouse models with spinal cord injury.[1][2] It has also been used as a serotonin receptor agonist to study its effects on the locomotion of zebrafish.[3]

Biochem/physiol Actions

Quipazine belongs to the class of psychedelics[4] and acts as a serotonin/5-hydroxytryptamine-2A/C receptor agonist.[2] It also acts as an inhibitor of prolactin.[5]

pictograms

Skull and crossbones
GHS06

signalword

Danger

hcodes

H301

Hazard Classifications

Acute Tox. 3 Oral

Storage Class

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000299649
0000299650
0000262363
107M4132V
13131102

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Jonathan A Norton et al.
Annals of the New York Academy of Sciences, 1198, 10-20 (2010-06-12)
Afferent inputs are known to modulate the activity of locomotor central pattern generators, but their role in the generation of locomotor patterns remains uncertain. This study sought to investigate the importance of afferent input for producing bilateral, coordinated hindlimb stepping
Chadanat Noonin
Developmental and comparative immunology, 86, 189-195 (2018-05-21)
Serotonin (5-HT) is a conserved monoamine neurotransmitter that has several physiological functions both in vertebrates and invertebrates. In addition to its well-known function in the central nervous system, 5-HT also participates in peripheral system. However, in crustaceans, the knowledge about
J M Zgombick et al.
Naunyn-Schmiedeberg's archives of pharmacology, 354(3), 226-236 (1996-08-01)
Recombinant human 5-HT1D alpha and 5-HT1D beta receptor subtypes were stably expressed in NIH-3T3 fibroblasts (1D alpha cell line) and Y-1 adrenocortical tumor cells (1D beta cell line), respectively, for pharmacological evaluations of serotonergic compounds to inhibit forskolin-stimulated cAMP accumulation
Urszula Sławińska et al.
The Journal of physiology, 590(7), 1721-1736 (2012-02-22)
Recent studies on the restoration of locomotion after spinal cord injury have employed robotic means of positioning rats above a treadmill such that the animals are held in an upright posture and engage in bipedal locomotor activity. However, the impact
Dilip Kumar Pandey et al.
Pharmacology, biochemistry, and behavior, 94(3), 363-373 (2009-10-06)
Collective evidence suggests that inhibition of neuronal 5-hydroxytryptamine type 2A (5-HT(2A)) receptors contributes to the assuagement of depression-like behaviour in rodents. The present study evaluated the antidepressant-like effect of the 5-((4-benzo [alpha] isothiazol-3-yl) piperazin-1-yl) methyl)-6-chloroindolin-2-one (BIP-1), a compound having affinity
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