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Submit ReviewAP C5 is a potent and selective protein kinase G type II (PKG2) inhibitor (pIC50 = 7.2). Displays >20-fold selectivity for PKG2 over PKG1 and PKA (pIC50 values are 4.6 and 4.8 for PKG1 and PKA, respectively). Blocks 8-pCPT-cGMP-dependent VASP phosphorylation in intestinal organoids. Also attenuates toxin-stimulated anion secretory responses in mouse intestinal tissue.
AP C5 is also offered as part of the Tocriscreen 2.0 Max and Tocriscreen Kinase Inhibitor Library. 了解 Tocris 化合物库的更多信息。
分子量 | 275.31 |
公式 | C16H13N5 |
储存 | Store at -20°C |
纯度 | ≥98% (HPLC) |
CAS Number | 2234272-10-5 |
PubChem ID | 137919866 |
InChI Key | QKHQFSQJQKGFAA-UHFFFAOYSA-N |
Smiles | C#CCNC1=NC(C2=CC=C(N3C=CN=C3)C=C2)=CC=N1 |
上方提供的技术数据仅供参考。批次相关数据请参见分析证书。
Tocris products are intended for laboratory research use only, unless stated otherwise.
溶剂 | 最高浓度 mg/mL | 最高浓度 mM | |
---|---|---|---|
溶解性 | |||
DMSO | 27.53 | 100 | |
1eq. HCl | 27.53 | 100 |
以下数据基于产品分子量 275.31。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
浓度/溶剂体积/质量 | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 3.63 mL | 18.16 mL | 36.32 mL |
5 mM | 0.73 mL | 3.63 mL | 7.26 mL |
10 mM | 0.36 mL | 1.82 mL | 3.63 mL |
50 mM | 0.07 mL | 0.36 mL | 0.73 mL |
参考文献是支持产品生物活性的出版物。
Bijvelds et al (2018) Selective inhibition of intestinal guanosine 3',5'-cyclic monophosphate signaling by small-molecule protein kinase inhibitors. J.Biol.Chem. 293 8173 PMID: 29653944
If you know of a relevant reference for AP C5, please let us know.
关键词: AP C5, AP C5 supplier, APC5, protein, kinase, g, type, 2, II, inhibitors, inhibits, guanosine, 3,5-cyclic, monophosphate, dependent, Protein, Kinase, G, 6626, Tocris Bioscience
平均评分: 5 (Based on 1 Review.)
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