生物活性 | |||
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描述 | SEN12333 is a potent, selective and orally active α7 nAChR agonist. SEN12333 has a high affinity for rat α7 nAChRs expressed in GH4C1 cells (Ki=260 nM) and acts as a full agonist in functional Ca2+ flux studies (EC50=1.6 μM). SEN 12333 was used in attention deficit disorder and schizophrenia studies. In whole-cell patch-clamp recordings, SEN12333 activated peak currents and maximum total charge similar to acetylcholine (EC50= 12 μM). SEN12333 has functional antagonistic effects on histamine H3 receptor (IC50=103 nM), and on the human ganglionic α3 nAChRs with weak agonistic activity (IC50= 8.5 μM)[1]. |
实验方案 | |||
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1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
2.95mL 0.59mL 0.29mL |
14.73mL 2.95mL 1.47mL |
29.46mL 5.89mL 2.95mL |
参考文献 |
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