Detailed Information on Publication Record
2023
Efficient synthesis of novel 2-deoxy-C-nucleosides containing oxa and thiadiazole derivatives and their biological activity
PENJARLA, Srishylam, Paidi Yella REDDY, Santhosh PENTA, Yogesh S. SANGHVI, Ludek EYER et. al.Basic information
Original name
Efficient synthesis of novel 2-deoxy-C-nucleosides containing oxa and thiadiazole derivatives and their biological activity
Authors
PENJARLA, Srishylam, Paidi Yella REDDY, Santhosh PENTA, Yogesh S. SANGHVI, Ludek EYER, Michal STEFANIK, Daniel RŮŽEK (203 Czech Republic, belonging to the institution) and Shyamapada BANERJEE (guarantor)
Edition
Journal of Molecular Structure, Amsterdam, Elsevier, 2023, 0022-2860
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10606 Microbiology
Country of publisher
Netherlands
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 3.800 in 2022
RIV identification code
RIV/00216224:14310/23:00132638
Organization unit
Faculty of Science
UT WoS
001032754800001
Keywords in English
C -nucleoside; Oxadiazoles; Thiadiazoles; Antiviral; Antitumor; Heterocycles
Tags
Tags
International impact, Reviewed
Změněno: 22/12/2023 09:16, Mgr. Marie Šípková, DiS.
Abstract
V originále
Five membered oxa- and thiadiazole derivatives have shown significant biological activity due to their unique bioisosteric properties. Herein, we describe an efficient synthetic approach leading to several novel C-nucleosides containing an oxadiazole or thiadiazole ring system. This work provides for the first-time ability to assemble & beta;-Cnucleosides in a facile manner offering an ideal framework for the possible development of new antiviral and antitumor drugs. All new C-nucleosides were tested for their activity against TBEV and SARS-CoV-2. Two of the synthesized compounds exerted mild anti-SARS-CoV-2 activity, as evidenced by the decrease in viral titers by <1 log10 PFU/ml compared with controls. Mechanism for the formation of 5-substituted 1,3,4-thiadiazole ring is proposed and a structure-activity relationship established with these C-nucleosides.