Description

Isoguanosine Hydrate (CAS No. 359436-55-8) is a high-purity nucleoside analog with the molecular formula C₁₀H₁₅N₅O₆, widely utilized in biochemical and pharmaceutical research. This compound is a hydrated form of isoguanosine, featuring a unique purine base structure that distinguishes it from canonical nucleosides. It serves as a critical intermediate in nucleic acid chemistry, enzymology studies, and the development of novel therapeutics. With its well-defined stereochemistry at the ribose moiety, Isoguanosine Hydrate is ideal for investigating nucleotide metabolism, RNA modification, and enzyme-substrate interactions. Packaged under strict quality control, this product guarantees ≥95% purity (HPLC) and is supplied as a lyophilized powder for optimal stability and solubility in aqueous buffers.

Properties

• CAS Number: 359436-55-8
• Complexity: 544
• IUPAC Name: 6-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]-1H-purin-2-one;hydrate
• InChI: InChI=1S/C10H13N5O5.H2O/c11-7-4-8(14-10(19)13-7)15(2-12-4)9-6(18)5(17)3(1-16)20-9;/h2-3,5-6,9,16-18H,1H2,(H3,11,13,14,19);1H2/t3-,5-,6-,9-;/m1./s1
• InChI Key: XJFGKAOCZWFNPZ-GWTDSMLYSA-N
• Exact Mass: 301.10223322
• Molecular Formula: C10H15N5O6
• Molecular Weight: 301.26
• SMILES: C1=NC2=C(NC(=O)N=C2N1[C@H]3[C@@H]([C@@H]([C@H](O3)CO)O)O)N.O
• Topological: 154
• Monoisotopic Mass: 301.10223322
• Synonyms: Isoguanosine Hydrate, 359436-55-8, 832-805-5, Isoguanosinehydrate(1:x), Isoguanosine hydrate(1:x), 6-Amino-9-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-3,9-dihydro-2H-purin-2-one hydrate, 6-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3,9-dihydro-2H-purin-2-one hydrate, DB-230556, F12754

Isoguanosine Hydrate is primarily used in research applications involving nucleic acid biochemistry and drug discovery. It serves as a substrate or inhibitor in enzymatic studies of nucleoside kinases and phosphorylases. The compound is also employed in the synthesis of modified oligonucleotides for probing RNA structure-function relationships. Additionally, its unique base pairing properties make it valuable for studying non-canonical nucleic acid interactions.

Safety and Hazards

GHS Hazard Statements

• Not Classified
• Reported as not meeting GHS hazard criteria by 1 of 1 companies. For more detailed information, please visit ECHA C&L website.

Hazard Classes and Categories

• Not Classified

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