<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13(24)</volume><submitter>Sawyer JM</submitter><pubmed_abstract>Fluorescent nucleosides are useful chemical tools for biochemical research and are frequently incorporated into nucleic acids for a variety of applications. The most widely utilized fluorescent nucleoside is 2-aminopurine-2'-deoxyribonucleoside (2APN). However, 2APN is limited by a moderate Stokes shift, molar extinction coefficient, and quantum yield. We recently reported 4-cyanoindole-2'-deoxyribonucleoside (4CIN), which offers superior photophysical characteristics in comparison to 2APN. To further improve upon 4CIN, a focused library of additional analogues combining the structural features of 2APN and 4CIN were synthesized and their photophysical properties were quantified. Nucleosides 2-6 were found to possess diverse photophysical properties with some features superior to 4CIN. In addition, the structure-function relationship data gained from 1-6 can inform the design of next-generation fluorescent indole nucleosides.</pubmed_abstract><journal>RSC advances</journal><pagination>16369-16376</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10230516</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Synthesis and photophysical characterization of fluorescent indole nucleoside analogues.</pubmed_title><pmcid>PMC10230516</pmcid><pubmed_authors>Passow KT</pubmed_authors><pubmed_authors>Sawyer JM</pubmed_authors><pubmed_authors>Harki DA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis and photophysical characterization of fluorescent indole nucleoside analogues.</name><description>Fluorescent nucleosides are useful chemical tools for biochemical research and are frequently incorporated into nucleic acids for a variety of applications. The most widely utilized fluorescent nucleoside is 2-aminopurine-2'-deoxyribonucleoside (2APN). However, 2APN is limited by a moderate Stokes shift, molar extinction coefficient, and quantum yield. We recently reported 4-cyanoindole-2'-deoxyribonucleoside (4CIN), which offers superior photophysical characteristics in comparison to 2APN. To further improve upon 4CIN, a focused library of additional analogues combining the structural features of 2APN and 4CIN were synthesized and their photophysical properties were quantified. Nucleosides 2-6 were found to possess diverse photophysical properties with some features superior to 4CIN. In addition, the structure-function relationship data gained from 1-6 can inform the design of next-generation fluorescent indole nucleosides.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 May</publication><modification>2025-04-18T17:46:23.481Z</modification><creation>2025-04-07T05:21:12.028Z</creation></dates><accession>S-EPMC10230516</accession><cross_references><pubmed>37266506</pubmed><doi>10.1039/d3ra03457g</doi></cross_references></HashMap>