3′-Amino modifications enhance the antifungal properties of N4-alkyl-5-methylcytidines for potential biocides

Author:

Alexandrova Liudmila A.1ORCID,Shevchenko Oleg V.1ORCID,Jasko Maxim V.1ORCID,Solyev Pavel N.1ORCID,Karpenko Inna L.1ORCID,Negrya Sergey D.1ORCID,Efremenkova Olga V.2ORCID,Vasilieva Byazilya F.2ORCID,Efimenko Tatiana A.2ORCID,Avdanina Darya A.3ORCID,Nuraeva Gulgina K.3ORCID,Potapov Mark P.3ORCID,Kukushkina Vera I.3ORCID,Kochetkov Sergey N.1ORCID,Zhgun Alexander A.3ORCID

Affiliation:

1. Engelhardt Institute of Molecular Biology RAS, 32 Vavilova St., 119991 Moscow, Russia

2. Gause Institute of New Antibiotics, 11 Bol'shaya Pirogovskaya St., 119021 Moscow, Russia

3. Research Center of Biotechnology RAS, 33 Leninsky Ave, 119071 Moscow, Russia

Abstract

A set of 3′-modified N4-alkyl-5-methyl-2′-deoxycytidines has been synthesized and evaluated for biological activity. The replacement of the 3′-hydroxyl group with amino, aminoethyl and dialkylamino groups significantly enhances antifungal activity.

Funder

Ministry of Education and Science of the Russian Federation

Russian Foundation for Basic Research

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

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