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MCE 国际站:8-CPT-Cyclic AMP (sodium)
CAS:93882-12-3
品牌:MedChemExpress (MCE)
存储条件:Please store the product under the recommended conditions in the Certificate of Analysis.
生物活性:8-CPT-Cyclic AMP (8-CPT-cAMP) sodium 是 cyclic AMP-dependent protein kinase (PKA) 的选择性激活剂。 8-CPT-Cyclic AMP sodium 也是环 GMP 特异性磷酸二酯酶 (PDE VA) 的有效抑制剂,IC50 为 0.9微米。 8-CPT-Cyclic AMP sodium 还抑制 PDE III 和 PDE IV,IC50Epac 具有很高的亲和力,是一种有效的 Epac 激活剂[1][2] 。
体外:a-Fas 和 TNF-α/CHX 可迅速(在 2 小时内)诱导中性粒细胞死亡至少 90%。常用的 cAMP 类似物 8-pCPT-cAMP (0.7 mM) 可延迟 TNF-/CHX 诱导和 a-Fas 诱导的细胞凋亡。它对 TNF-/CHX 诱导的细胞凋亡比对 a-Fas[2] 更有效。
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研究领域:TGF-beta/Smad | Stem Cell/Wnt | Metabolic Enzyme/Protease
作用靶点:PKA | Phosphodiesterase (PDE)
Trending products:Recombinant Proteins | Bioactive Screening Libraries | Natural Products | Fluorescent Dye | PROTAC | Isotope-Labeled Compounds | Oligonucleotides
参考文献:[1]. Connolly BJ, et al. 8-(4-Chlorophenyl)thio-cyclic AMP is a potent inhibitor of the cyclic GMP-specific phosphodiesterase (PDE VA). Biochem Pharmacol. 1992;44(12):2303-2306.
[2]. Krakstad C, et al. cAMP protects neutrophils against TNF-alpha-induced apoptosis by activation of cAMP-dependent protein kinase, independently of exchange protein directly activated by cAMP (Epac). J Leukoc Biol. 2004;76(3):641-647.
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