Literature DB >> 21273064

Design and synthesis of highly solvatochromic fluorescent 2'-deoxyguanosine and 2'-deoxyadenosine analogs.

Katsuhiko Matsumoto1, Naoya Takahashi, Azusa Suzuki, Takashi Morii, Yoshio Saito, Isao Saito.   

Abstract

We synthesized various substituted 8-styryl-2'-deoxyguanosine and 8-styryl-2'-deoxyadenosine derivatives. Among them only acetyl substituted 8-styryl-2'-deoxyguanosine analog 5b showed a remarkable solvatochromicity (Δλ(max)(em)=91 nm),that is, strong fluorescence at 477 nm in 1,4-dioxane, but in methanol the fluorescence was red shifted to 558 nm with very low intensity. Such environmentally sensitive solvatochromic fluorescent guanosine analogs may be useful as a sensor for investigating interactions of DNA with DNA binding proteins.
Copyright © 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 21273064     DOI: 10.1016/j.bmcl.2010.11.129

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  3 in total

1.  Tracking the formation of supramolecular G-quadruplexes via self-assembly enhanced emission.

Authors:  Diana Silva-Brenes; Loruhama Delgado; José M Rivera
Journal:  Org Biomol Chem       Date:  2017-01-25       Impact factor: 3.876

2.  Heterocycle-modified 2'-Deoxyguanosine Nucleolipid Analogs Stabilize Guanosine Gels and Self-assemble to Form Green Fluorescent Gels.

Authors:  Manisha B Walunj; Seergazhi G Srivatsan
Journal:  Chem Asian J       Date:  2021-12-16

3.  New class of 8-aryl-7-deazaguanine cell permeable fluorescent probes.

Authors:  Ilirian Dhimitruka; Timothy D Eubank; Amy C Gross; Valery V Khramtsov
Journal:  Bioorg Med Chem Lett       Date:  2015-08-21       Impact factor: 2.823

  3 in total

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