Rp-8-CPT-Cyclic AMP (sodium salt)
中文名稱 | Rp-8-CPT-Cyclic AMP (sodium salt) |
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中文同義詞 | RP-8-CPT-CAMPS SODIUM |CAS 221905-35-7 |
英文名稱 | Rp-8-CPT-Cyclic AMP (sodium salt) |
英文同義詞 | Rp-8-CPT-Cyclic AMP (sodium salt);VXMLCXRTUQHZAI-ALHPSJIMSA-N;Rp-8-CPT-cAMPS sodium;Rp-8-CPT-Cyclic AMP sodium salt (Rp-8-CPT-cAMP) |
CAS號(hào) | 221905-35-7 |
分子式 | C16H16ClN5NaO5PS2 |
分子量 | 511.87 |
EINECS號(hào) | |
相關(guān)類別 | |
Mol文件 | 221905-35-7.mol |
結(jié)構(gòu)式 | ![]() |
Rp-8-CPT-Cyclic AMP (sodium salt) 性質(zhì)
儲(chǔ)存條件 | Store at -20°C |
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溶解度 | DMF:30mg/mL; DMSO:25mg/mL;乙醇:0.5mg/mL; PBS(pH 7.2):10 mg/mL |
形態(tài) | 結(jié)晶固體 |
顏色 | 白色至米白色 |
PKA
Rp-8-CPT-cAMPS (100 μM; 15 min) blocks phosphorylation of VASP by 6-Bnz-cAMP and largely reduces VASP phosphorylation by forskolin and fenoterol.
Rp-8-CPT-cAMPS (100 μM; 30 min) reduces GTP-loading of Rap1 by both 8-pCPT-2'-O-Me-cAMP and 6-Bnz-cAMP.
Rp-8-CPT-cAMPS (100 μM; 30 min) largely diminishes the augmentation of bradykinin-induced IL-8 release by the PKA activator 6-Bnz-cAMP and the Epac activator 8-pCPT-2'-O-Me-cAMP.
Rp-8-CPT-cAMPS (10 μM) inhibits the endothelium-dependent and -independent relaxation which induced by Venom in pre-contracted rat mesenteric artery rings.