化学性质
| Physical Appearance | Solution |
| Storage | Store at -20°C or below |
| M.Wt | 505.2 (free acid) |
| Formula | C11H18N5O12P3(free acid) |
| Synonyms | N6-Methyl-2'-deoxyadenosine-5'-Triphosphate |
| Chemical Name | lithium (3-hydroxy-5-(6-(methylamino)-9H-purin-9-yl)tetrahydrofuran-2-yl)methyl triphosphate |
| Canonical SMILES | OC1C(COP([O-])(OP([O-])(OP([O-])([O-])=O)=O)=O)OC(N2C=NC3=C2N=CN=C3NC)C1.[Li+].[Li+].[Li+].[Li+] |
| 运输条件 | 蓝冰运输或根据您的需求运输。 |
| 一般建议 | 为了使其更好的溶解，请用37℃加热试管并在超声波水浴中震动片刻。不同厂家不同批次产品溶解度各有差异，仅做参考。若实验所需浓度过大至产品溶解极限，请添加助溶剂助溶或自行调整浓度。溶液形式一般不宜长期储存，请尽快用完。 |
资料参考
Base modified ribonucleoside triphosphates, can be used in epigenetics research. N6-methyl ATP can substitute for ATP in some biological systems, and is a potent agonist for P2Y-purinoceptors in the guinea pig, taenia coli. In vitro studies showed that N6-methyl ATP substituted for ATP and supported cytoskeletal filament-driven translocation of motor proteins (dynein, kinesin and myosin). N6-methyl ATP is also a substrate for RNA polymerase and can be used for preparation of modified RNA.
m.cnreagent.com