Adenosine-5’-[γ-(propargyl)-imido]triphosphate sodium salt

产品名称：

γ-[(Propargyl)-imido]-ATP sodium salt
Adenosine-5’-[γ-(propargyl)-imido]triphosphate sodium salt

产品介绍：

产品说明

应用

Lee, et al,. reported a non-radioactive version of in vitro phosphorylation where γ-[(Propargyl)-imido]-ATP (compound 1) was successfully used instead of γ-³²P-modified ATP to phosphorylate GST-tagged recombinant p27kip1 with protein kinase cdk2. The phosphorylated, alkyne-modified protein substrate can be labeled with azides of biotin or fluorescent dyes using Cu(I)-catalyzed click chemistry.

包装

1 mg in glass bottle

法律信息

The purchase of this product for use in applications relating to copper catalyzed azide-alkyne cycloaddition chemistry ("Click Chemistry") includes a limited, nontransferable license to intellectual property owned by The Scripps Research Institute to use this product solely for internal non-commercial research activities and specifically excludes clinical, therapeutic, or diagnostic use in humans or animals and manufacturing purposes. Information regarding a license for commercial use in Click Chemistry may be obtained directly from The Scripps Research Institute, 10550 N. Torrey Pines Rd., La Jolla, CA 92037, or by contacting 858-784-8140 or click@scripps.edu.

基本信息

经验(实验)分子式	C₁₃H₁₉N₆O₁₂P₃ · xNa⁺
分子量	544.24 (free acid basis)
PubChem化学物质编号	329769104
NACRES	NA.22

产品性质

质量水平	200
测定	≥95% (HPLC)
形式	solid
reaction suitability	reaction type: click chemistry
溶解性	10 mM Tris-HCl, pH 7.5: soluble
运输	wet ice
储存温度	−20℃
SMILES string	NC1=NC=NC2=C1N=CN2[C@H]3O[C@H](COP(OP(O)(OP(O)(NCC#C)=O)=O)(O)=O)[C@@H](O)[C@H]3O
InChI	1S/C13H19N6O12P3/c1-2-3-18-32(22,23)30-34(26,27)31-33(24,25)28-4-7-9(20)10(21)13(29-7)19-6-17-8-11(14)15-5-16-12(8)19/h1,5-7,9-10,13,20-21H,3-4H2,(H,24,25)(H,26,27)(H2,14,15,16)(H2,18,22,23)/t7-,9-,10-,13?/m1/s1
InChI key	PIPOEUYSJJTELD-RJNFYWFKSA-N

安全信息

储存分类代码	13 - Non Combustible Solids
WGK	WGK 3
闪点(F)	Not applicable
闪点(C)	Not applicable