| 产品描述: | TRPV1 antagonist 3 (Compound 7q) is a potent TRPV1 antagonist with an IC50 of 2.66 nM against capsaicin. TRPV1 antagonist 3 is mode-selective, oral bioavailable (F = 60%) and CNS-penetrant. |
| 靶点: |
hTRPV1:2.66 nM (IC50); TRPM8:7.45 μM (IC50) |
| 体外研究: |
TRPV1 antagonist 3 (Compound 7q) (0-30 mg/kg; i.p.; 30 min) shows anti-nociceptive effect mainly mediated by blocking CAP-activated channel. TRPV1 antagonist 3 (0-100 mg/kg; i.g.) had no obvious thermal effect in rats. TRPV1 antagonist 3 (10 mg/kg; i.v.) shows a good concentration in the brain at 0.5 h, with value of 2311 ng/g, and has good CNS penetration, with a brain/plasma ratio of 1.66. |
| 体内研究: |
TRPV1 antagonist 3 (Compound 7q) is highly selective for the TRPV1 receptor relative to other TRP channels. TRPV1 antagonist 3 shows acceptable aqueous solubility (solubility at pH 7.4 = 26 μg/mL) . |
| 保存条件: |
-80°C 6个月;-20°C 1个月 |
| 配置溶液浓度参考: |
|
1mg |
5mg |
10mg |
| 1 mM |
2.554 ml |
12.77 ml |
25.541 ml |
| 5 mM |
0.511 ml |
2.554 ml |
5.108 ml |
| 10 mM |
0.255 ml |
1.277 ml |
2.554 ml |
| 50 mM |
0.051 ml |
0.255 ml |
0.511 ml |
|
| 注意: |
部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。 |