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Merck
CN

SML1087

Sigma-Aldrich

马来酸舒马尼罗

≥98% (HPLC)

别名:

CID 9818479马来酸酯, PNU-95,666马来酸酯, (5R)-5,6-二氢-5-(甲基氨基)-4H-咪唑并[4,5,1-ij]喹啉-2(1H)-马来酸酯, (R)-5,6-二氢-5-(甲氨基)-4H-咪唑并[4,5,1-ij]喹啉-2(1H)-马来酸酯

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About This Item

经验公式(希尔记法):
C11H13N3O · C4H4O4
分子量:
319.31
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77

质量水平

方案

≥98% (HPLC)

表单

powder

旋光性

[α]/D -22 to -32°, c = 1 in H2O

储存条件

desiccated

颜色

white to beige

溶解性

H2O: 10 mg/mL, clear

储存温度

−20°C

SMILES字符串

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

InChI key

VOJRMYBBPKNLLI-ORHWHDKWSA-N

应用

苏马尼罗马来酸酯已被用作多巴胺2型受体(D2R)激动剂,用于研究其对大鼠空间学习和记忆的影响。

生化/生理作用

Sumanirole是一种高度选择性的强效多巴胺D2受体激动剂,可降低黑质致密部中的血浆催乳素水平和降低的多巴胺神经元放电速率。Sumanirole在帕金森病动物模型中可有效刺激运动活动。

特点和优势

该化合物是神经科学研究推荐产品。点击此处 ,查看更多神经科学精选产品。想要了解有关生物活性小分子在其他研究领域应用的更多信息,请访问 sigma.com/discover-bsm

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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访问文档库

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)
L Lencesova et al.
Life sciences, 191, 186-194 (2017-10-22)
Haloperidol is an antipsychotic agent and acts as dopamine D2 receptor (D2R) antagonist, as a prototypical ligand of sigma1 receptors (Sig1R) and it increases expression of type 1 IP We used differentiated NG-108 cells and H9c2 cells. Gene expression, Western
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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