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Rp-cAMPS triethylammonium salt is an analog of cAMP.It acts as a potent, competitive and cell-permeable antagonist of cAMP-induced activation of cAMP-dependent PKA I and II with Kis of 6.05 μM and 9.75 μM, respectively.
Rp-cAMPS triethylammonium salt is an analog of cAMP.It acts as a potent, competitive and cell-permeable antagonist of cAMP-induced activation of cAMP-dependent PKA I and II with Kis of 6.05 μM and 9.75 μM, respectively.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
500 μg | ¥ 2,500 | 35日内发货 | |
1 mg | ¥ 3,980 | 35日内发货 | |
5 mg | ¥ 11,186 | 35日内发货 |
产品描述 | Rp-cAMPS triethylammonium salt is an analog of cAMP.It acts as a potent, competitive and cell-permeable antagonist of cAMP-induced activation of cAMP-dependent PKA I and II with Kis of 6.05 μM and 9.75 μM, respectively. |
靶点活性 | PKA II:9.75 µM (ki), PKA I:ki: 6.05 µM |
体外活性 | A membrane-permeable competitive antagonist of cAMP that blocks PKA activation by binding to the regulatory subunits without dissociating the kinase holoenzyme inhibits synaptic plasticity[1]. |
体内活性 | The monosynaptic EPSCs evoked at the PB-CeLC and BLA-CeLC synapses in slices from arthritic rats decreased by Rp-cAMPS (10 μM, 15 min) but not in control neurons from normal animals. The inhibitory effect of Rp-cAMPS is significant compared to predrug (ACSF) control values obtained in the same neurons[1]. |
分子量 | 446.46 |
分子式 | C16H27N6O5PS |
CAS No. | 151837-09-1 |
密度 | no data available |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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