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描述 | RQ-00203078, a potent, orally active, and highly selective antagonist of TRPM8 channels, exhibits IC50s of 5.3 nM and 8.3 nM for rat and human TRPM8 channels, respectively, while showing minimal inhibitory effects on TRPV1, TRPA1, TRPV4, and TRPM2 channels[1].[2]. |
Animal study | Demonstrating impressive in vivo efficacy, RQ-00203078 showed a dose-dependent effect with an ED50 of 0.65 mg/kg in rats subjected to the Icilin-induced wet-dog shakes model following oral administration[1]. Additionally, pharmacokinetic studies in rats revealed significant oral exposure of RQ-00203078 (compound 36) at a dose of 3 mg/kg (p.o.), with a Cmax of 2300 ng/mL and a bioavailability of 86%[1]. |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
1.80mL 0.36mL 0.18mL |
9.01mL 1.80mL 0.90mL |
18.02mL 3.60mL 1.80mL |
CAS号 | 1254205-52-1 |
分子式 | C21H13ClF6N2O5S |
分子量 | 554.85 |
SMILES Code | O=C(O)C1=CC=C(S(=O)(N(C2=NC=C(C(F)(F)F)C=C2Cl)CC3=CC=C(OC(F)(F)F)C=C3)=O)C=C1 |
MDL No. | MFCD29049510 |
别名 | |
运输 | 蓝冰 |
InChI Key | IJGQFZYYEHCCIZ-UHFFFAOYSA-N |
Pubchem ID | 49783953 |
存储条件 |
In solvent -20°C:3-6个月-80°C:12个月 Pure form Inert atmosphere, 2-8°C |
溶解方案 |
请根据您的动物给药指南选择适当的溶解方案。 以下溶解方案都请先按照体外实验的方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议现用现配,当天使用; 以下溶剂前显示的百分比是指该溶剂在终溶液中的体积占比;如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶
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