Guanosine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-N-(2-methyl-1-oxopropyl)-

• CAT Number: L038709
• CAS Number: 68892-41-1
• Molecular Formula: C35H37N5O7
• Molecular Weight: 639.70
• Purity: ≥95%
• Target: DNA/RNA Synthesis
• IUPAC Name: N-[9-[(2R,4S,5R)-5-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-4-hydroxyoxolan-2-yl]-6-oxo-1H-purin-2-yl]-2-methylpropanamide
• InChI: InChI=1S/C35H37N5O7/c1-21(2)32(42)38-34-37-31-30(33(43)39-34)36-20-40(31)29-18-27(41)28(47-29)19-46-35(22-8-6-5-7-9-22,23-10-14-25(44-3)15-11-23)24-12-16-26(45-4)17-13-24/h5-17,20-21,27-29,41H,18-19H2,1-4H3,(H2,37,38,39,42,43)/t27-,28+,29+/m0/s1
• InChIKey: RMQXDNUKLIDXOS-ZGIBFIJWSA-N
• SMILES: CC(C)C(=O)NC1=NC2=C(C(=O)N1)N=CN2[C@H]3C[C@@H]([C@H](O3)COC(C4=CC=CC=C4)(C5=CC=C(C=C5)OC)C6=CC=C(C=C6)OC)O

Guanosine, 5′-O-[bis(4-methoxyphenyl)phenylmethyl]-2′-deoxy-N-(2-methyl-1-oxopropyl)（Cat No.:L038709）is a modified guanosine derivative commonly used in nucleoside analog research. It features protective groups like bis(4-methoxyphenyl)phenylmethyl and 2-methyl-1-oxopropyl, which allow for selective deprotection during synthesis. This compound is valuable in studying nucleic acid chemistry and drug development, particularly in the design of antiviral and anticancer agents. Its modified structure enables it to participate in reactions that probe nucleoside function, DNA replication, and RNA transcription, making it a versatile tool in biochemical and pharmaceutical research.