inosine (Chem Impex International)
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95
Structured Review
Chem Impex International
inosine
Inosine, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/00103/2'-Deoxyinosine/pm40193230-64-0-6
Average 95 stars, based on 2 article reviews
Inosine, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/00103/2'-Deoxyinosine/pm40193230-64-0-6
Average 95 stars, based on 2 article reviews
inosine - by Bioz Stars,
2026-09
95/100 stars
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other:Article Title: Structural and Energetic Effects of the 2-Amino and 2'- and 3'-Hydroxy Substituents of Protonated Guanosine Nucleosides: IRMPD, ER-CID, and Theoretical Studies of Protonated Guanosine and Inosine Nucleosides. Article Snippet: Inosine is a naturally occurring modified RNA nucleoside.. Guanosine differs from inosine only by the 2-amino substituent of its nucleobase.. The effects of the 2-amino and 2′and 3′-hydroxy substituents on structure and glycosidic bond stability are examined via comparative studies of protonated guanosine vs inosine nucleoside analogues. DNA Synthesis:Article Title: The Efficiency of Light-Directed Synthesis of DNA Arrays on Glass Substrates Article Snippet: New methods based on photolithography and surface fluorescence were used to determine photodeprotection rates and stepwise yields for light-directed oligonucleotide synthesis using photolabile 5′-(((R-methyl-2-nitropiperonyl)oxy)carbonyl)(MeNPOC)-2′-deoxynucleoside phosphoramidites on planar glass substrates.. Under near-UV illumination (primarily 365 nm) from a mercury light source, the rate of photoremoval of the MeNPOC protecting group was found to be independent of both the nucleotide and length of the growing oligomer (t1/2 ) 12 s at 27.5 mW/cm2).. A moderate dependence on solvent polarity was observed, with photolysis proceeding most rapidly in the presence of nonpolar solvents or in the absence of solvent (e.g., t1/2 ) 10-13 s at 27.5 mW/cm2). Pore Size:Article Title: The Efficiency of Light-Directed Synthesis of DNA Arrays on Glass Substrates Article Snippet: New methods based on photolithography and surface fluorescence were used to determine photodeprotection rates and stepwise yields for light-directed oligonucleotide synthesis using photolabile 5′-(((R-methyl-2-nitropiperonyl)oxy)carbonyl)(MeNPOC)-2′-deoxynucleoside phosphoramidites on planar glass substrates.. Under near-UV illumination (primarily 365 nm) from a mercury light source, the rate of photoremoval of the MeNPOC protecting group was found to be independent of both the nucleotide and length of the growing oligomer (t1/2 ) 12 s at 27.5 mW/cm2).. A moderate dependence on solvent polarity was observed, with photolysis proceeding most rapidly in the presence of nonpolar solvents or in the absence of solvent (e.g., t1/2 ) 10-13 s at 27.5 mW/cm2). Chromatography:Article Title: The Efficiency of Light-Directed Synthesis of DNA Arrays on Glass Substrates Article Snippet: New methods based on photolithography and surface fluorescence were used to determine photodeprotection rates and stepwise yields for light-directed oligonucleotide synthesis using photolabile 5′-(((R-methyl-2-nitropiperonyl)oxy)carbonyl)(MeNPOC)-2′-deoxynucleoside phosphoramidites on planar glass substrates.. Under near-UV illumination (primarily 365 nm) from a mercury light source, the rate of photoremoval of the MeNPOC protecting group was found to be independent of both the nucleotide and length of the growing oligomer (t1/2 ) 12 s at 27.5 mW/cm2).. A moderate dependence on solvent polarity was observed, with photolysis proceeding most rapidly in the presence of nonpolar solvents or in the absence of solvent (e.g., t1/2 ) 10-13 s at 27.5 mW/cm2). |