Cas No.: | 10527-47-6 |
Chemical Name: | Guanosine 5'-triphosphate-5'-adenosine |
SMILES: | O[C@H]1[C@](O[C@@H]([C@H]1O)COP(OP(OP(OC[C@H]2O[C@](N3C4=NC=NC(N)=C4N=C3)([H])[C@@H]([C@@H]2O)O)(O)=O)(O)=O)(O)=O)([H])N5C6=C(C(N=C(N6)N)=O)N=C5 |
Formula: | C20H27N10O17P3 |
M.Wt: | 772.41 |
Purity: | >98% |
Sotrage: | 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO |
Description: | Guanosine 5'-triphosphate-5'-adenosine, the 5′ cap analog, is a fluorescent substrate analog[1]. |
In Vitro: | Guanosine 5'-triphosphate-5'-adenosine (GpppA) labeled with pyrene at the 3′‐O position of adenosine acted as an artificial substrate[1]. Fluorescently labeled Guanosine 5'-triphosphate-5'-adenosine (GpppA) and GpppG analogs as potential substrates that represent a reasonable compromise between the structural complexity and requirements of the enzyme[1]. |
References: | [1]. Renata Kasprzyk, et al. Direct High-Throughput Screening Assay for mRNA Cap Guanine-N7 Methyltransferase Activity. Chemistry. 2020 Sep 1;26(49):11266-11275. [2]. Dennis Reichert, et al. Light-control of cap methylation and mRNA translation via genetic code expansion of Ecm1. Chem Sci. 2021 Feb 8;12(12):4383-4388. |