Urotensin II, mouse acetate 是孤儿 G 蛋白偶联受体 GPR14 或 SENR 的一种内源性配体。Urotensin II, mouse acetate 是一种有效的血管收缩剂。在中枢神经系统中起着重要作用。
Urotensin II, mouse acetate Chemical Structure
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数量
1 mg
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5 mg
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50 mg
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Urotensin II, mouse acetate 相关产品
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Bioactive Compound Library Plus
GPCR/G Protein Compound Library
Anti-Cardiovascular Disease Compound Library
Peptide Library
生物活性
Urotensin II, mouse acetate is an endogenous ligand for the orphan G-protein-coupled receptor GPR14 or SENR. Urotensin II, mouse acetate is a potent vasoconstrictor. Urotensin II, mouse acetate plays a physiological role in the central nervous system[1].
IC50 Target
GPR14[1]
体内研究 (In Vivo)
Urotensin II is a somatostatin-like cyclic peptide which functions as an arterial vasocontrictor, vasodilator, and bronchoconstriction mediator[1]. Urotensin II (0.1 nmol, 0.3 nmol, and 3 nmol; intracerebroventricular administration) induces anxiogenic-like behaviors in the elevated plus maze test and the hole-board test in mice in a dose-dependent manner[1].
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Animal Model:
Male C57BL/6N mice (8 weeks old)[1]
Dosage:
0.1 nmol, 0.3 nmol, and 3 nmol
Administration:
Intracerebroventricular (i.c.v.) administration
Result:
Decreased the amount of head dipping without significant alteration of the motor activity.
分子量
1693.91
Formula
C2H4O2
运输条件
Room temperature in continental US; may vary elsewhere.
[1]. Matsumoto Y, et al. Intracerebroventricular administration of urotensin II promotes anxiogenic-like behaviors in rodents. Neurosci Lett. 2004 Mar 25;358(2):99-102.