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产品名称
cAMP依赖性蛋白激酶抑制剂PKI-tide,
方案
≥95% (HPLC)
表单
lyophilized
组成
Peptide Content, ≥67%
储存条件
protect from light
储存温度
−20°C
Amino Acid Sequence
Ile-Ala-Ala-Gly-Arg-Thr-Gly-Arg-Arg-Gln-Ala-Ile-His-Asp-Ile-Leu-Val-Ala-Ala
应用
IAAGRTGRRQAIHDILVAA用作cAMP依赖性蛋白激酶抑制肽。
生化/生理作用
cAMP依赖性蛋白激酶抑制剂通常被设计为靶向第二信使cAMP(环磷酸腺苷)的合成和降解。
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Signaling through cAMP and cAMP-dependent protein kinase: diverse strategies for drug design
Biochimica et Biophysica Acta (BBA)-Proteins and Proteomics, 1784(1), 16-26 (2008)
ChemMedChem, 16(1), 292-300 (2020-10-09)
In lead optimization, protein crystallography is an indispensable tool to analyze drug binding. Binding modes and non-covalent interaction inventories are essential to design follow-up synthesis candidates. Two protocols are commonly applied to produce protein-ligand complexes: cocrystallization and soaking. Because of
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