CAS NO: | 142439-94-9 |
生物活性 | Rp-cAMPS sodium salt, a cAMP analog, is a potent, competitive cAMP-induced activation of cAMP-dependentPKAI and II(Kis of 12.5 μM and 4.5 μM, respectively) antagonist. Rp-cAMPS sodium salt is resistant to hydrolysis by phosphodiesterases[1][2][3][4][5][6]. | ||||||||||||||||
IC50& Target | Ki: 6.05 μM (PKA I) and 9.75 μM (PKA II)[1] | ||||||||||||||||
体外研究 (In Vitro) | A membrane-permeable competitive cAMP antagonist (Rp-cAMPS) that blocks PKA activation by binding to the regulatory subunits without dissociating the kinase holoenzyme also inhibits synaptic plasticity but has no effect on normal synaptic transmission[2]. | ||||||||||||||||
体内研究 (In Vivo) | Rp-cAMPS (10 μM, 15 min) decreases the monosynaptic EPSCs evoked at the PB-CeLC and BLA-CeLC synapses in slices from arthritic rats 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[2]. | ||||||||||||||||
分子量 | 367.25 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C10H11N5NaO5PS | ||||||||||||||||
CAS 号 | 142439-94-9 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 | -20°C, sealed storage, away from moisture and light *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light) | ||||||||||||||||
溶解性数据 | In Vitro: H2O : 250 mg/mL(680.74 mM;Need ultrasonic) 配制储备液
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