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CAS No. : 2469274-58-4
MCE 国际站:Palosuran hydrochloride
产品活性:Palosuran hydrochloride (ACT-058362 hydrochloride) 是一种有效,选择性和具有口服活性的 urotensin II receptor 受体拮抗剂,对于表达人重组受体的 CHO 细胞膜的 IC50 值为 3.6 nM。Palosuran hydrochloride 可改善糖尿病大鼠的胰腺和肾脏功能。
研究领域:GPCR/G Protein
作用靶点:Urotensin Receptor
In Vitro: Palosuran (8 h) inhibits 125I-U-II binding to human UT receptor, with IC50s of 46.2 nM on TE 671 cells and 86 nM on recombinant CHO cells.
Palosuran inhibits Ca2+ mobilization in response to human U-II in CHO cells expressing human and rat UT receptor with IC50s of 17 and >10000 nM, respectively.
Palosuran (0.12-10000 nM; 20 min) inhibits human U-II induced MAPK phosphorylation in a dose-dependent manner in recombinant CHO cells, with an IC50 of 150 nM.
In Vivo: ACT-058362 (10 mg/kg/h; i.v.) fully prevents the decrease in renal blood flow after ischemia in rats without decreasing blood pressure.
Palosuran (300 mg/kg/d; p.o. for 16 weeks) improves the survival, increases insulin, and slows the increase in glycemia, glycosylated hemoglobin, and serum lipids in streptozotocin-induced diabetic rats.
相关产品:Bioactive Compound Library Plus | GPCR/G Protein Compound Library | Anti-diabetic Compound Library | Anti-Cardiovascular Disease Compound Library | Orally Active Compound Library | Targeted Diversity Library | Human Metabolite Library | Heterocyclic Compound Library | Membrane Protein-targeted Compound Library | Membrane Receptor-targeted Compound Library | Highly Selective Inhibitors Library | PRL 2915 | Palosuran | UFP-803 TFA | SB-657510 | Urotensin II, mouse | Urotensin II (114-124), human TFA | PRL 3195 | SB-611812 | [Orn5]-URP
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