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About This Item
Empirical Formula (Hill Notation):
C11H13N3O · C4H4O4
CAS Number:
Molecular Weight:
319.31
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
MDL number:
Product Name
Sumanirole maleate, ≥98% (HPLC)
InChI key
VOJRMYBBPKNLLI-ORHWHDKWSA-N
SMILES string
O=C1N(C[C@H](NC)C2)C3=C2C=CC=C3N1.O=C(O)/C=C\C(O)=O
InChI
1S/C11H13N3O.C4H4O4/c1-12-8-5-7-3-2-4-9-10(7)14(6-8)11(15)13-9;5-3(6)1-2-4(7)8/h2-4,8,12H,5-6H2,1H3,(H,13,15);1-2H,(H,5,6)(H,7,8)/b;2-1-/t8-;/m1./s1
assay
≥98% (HPLC)
form
powder
optical activity
[α]/D -22 to -32°, c = 1 in H2O
storage condition
desiccated
color
white to beige
solubility
H2O: 10 mg/mL, clear
storage temp.
−20°C
Quality Level
Related Categories
Application
Sumanirole maleate has been used as a dopamine type 2 receptor (D2R) agonist to study its effects on spatial learning and memory in rats.
Biochem/physiol Actions
Sumanirole is a highly selective and potent dopamine D2 receptor agonist that decreased plasma prolactin levels and depressed dopamine neuron firing rates in the substantia nigra pars compacta. Sumanirole potently stimulates locomotor activity in in animal models of Parkinson′s disease.
Sumanirole is a highly selective and potent dopamine D2 receptor agonist.
Features and Benefits
This compound is a featured product for Neuroscience research. Click here to discover more featured Neuroscience products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Matthew F Lazenka et al.
The Journal of pharmacology and experimental therapeutics, 362(1), 14-23 (2017-04-16)
Clinically significant pain often includes a decrease in both behavior and mesolimbic dopamine signaling. Indirect and/or direct dopamine receptor agonists may alleviate pain-related behavioral depression. To test this hypothesis, the present study compared effects of indirect and direct dopamine agonists
Dopamine type 1-and 2-like signaling in the modulation of spatial reference learning and memory
Feyissa D D, et al.
Behavioural Brain Research, 362, 173-180 (2019)
Spatial working memory in male rats: pre-experience and task dependent roles of dopamine D1-and D2-like receptors
Bezu M, et al.
Frontiers in Behavioral Neuroscience, 11, 196-196 (2017)
Anna Niewiarowska-Sendo et al.
Biochimica et biophysica acta, 1864(10), 1855-1866 (2017-08-02)
In recent years a wide range of studies have shown that G protein-coupled receptors modulate a variety of cell functions through the formation of dimers. For instance, there is growing evidence for the dimerization of bradykinin or dopamine receptors, both
Yasunori Haranishi et al.
Pharmacology, biochemistry, and behavior, 195, 172964-172964 (2020-06-07)
The descending serotonergic pathway, from the brainstem to spinal cord, modulates various aspects of pain processing. The spinal 5-hydroxytryptamine (5-HT)1A and 5-HT2A receptors play pivotal roles in pain modulation. Perospirone is a novel atypical antipsychotic that serves as a 5-hydroxytryptamine
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