Pharmacological properties of TQS and 4BP-TQS on nAChR subtypes.
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*Fold potentiation of response to ACh (100 µM) by TQS (100 µM).**Percentage inhibition of response to ACh (100 µM) by TQS (100 µM).†Agonist response of 4BP-TQS (100 µM) expressed as a fold response normalised to maximal concentration of ACh (3 mM).††Percentage inhibition of response to ACh (100 µM) by 4BP-TQS (100 µM). Data are means ± SEM.
创建时间：
2015-12-02
