473278-54-5
Chemical Structure
2′-O-(2-Methoxyethyl)guanosine
Synonym(s): 2'-O-MOE-rG
- CAS No.: 473278-54-5
- Formula:C13H19N5O6
- Molecular Weight:341.32
IUPAC Name: 2-amino-9-((2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-(2-methoxyethoxy)tetrahydrofuran-2-yl)-1,9-dihydro-6H-purin-6-one
InChIKey: DLLBJSLIKOKFHE-WOUKDFQISA-N
SMILES: O[C@H]1[C@@H](OCCOC)[C@H](N2C(N=C(N)NC3=O)=C3N=C2)O[C@@H]1CO
Biological Activity: 2′-O-(2-Methoxyethyl)guanosine (2'-O-MOE-rG) is a 2'-O-methoxyethyl-modified nucleoside analogue and an important intermediate in the synthesis of nucleic acid drugs. 2′-O-(2-Methoxyethyl)guanosine neither effectively phosphorylated by cytosolic nucleoside kinases, nor are they incorporated into cellular DNA or RNA[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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2′-O-(2-Methoxyethyl)guanosine | 99.81% | 2′-O-(2-Methoxyethyl)guanosine (2'-O-MOE-rG) is a 2'-O-methoxyethyl-modified nucleoside analogue and an important intermediate in the synthesis of nucleic acid drugs. 2′-O-(2-Methoxyethyl)guanosine neither effectively phosphorylated by cytosolic nucleoside kinases, nor are they incorporated into cellular DNA or RNA. | ||||||||||||||||||||
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- [1]. McPherson AK, et, al. An Improved Process for the Manufacture of 5′-O-(4,4′-Dimethoxytrityl)-N2-isobutyryl-2′-O-(2-methoxyethyl)guanosine. Org. Process Res. Dev. 2020, 24, 11, 2583-2590.
- [2]. Saleh AF, et, al. 2'-O-(2-Methoxyethyl) Nucleosides Are Not Phosphorylated or Incorporated Into the Genome of Human Lymphoblastoid TK6 Cells. Toxicol Sci. 2018 May 1;163(1):70-78. [Content Brief]
Keywords
