Počet záznamů: 1
Nucleotide analogues containing a pyrrolidine, piperidine or piperazine ring: Synthesis and evaluation of inhibition of plasmodial and human 6-oxopurine phosphoribosyltransferases and in vitro antimalarial activity
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SYSNO ASEP 0542010 Druh ASEP J - Článek v odborném periodiku Zařazení RIV J - Článek v odborném periodiku Poddruh J Článek ve WOS Název Nucleotide analogues containing a pyrrolidine, piperidine or piperazine ring: Synthesis and evaluation of inhibition of plasmodial and human 6-oxopurine phosphoribosyltransferases and in vitro antimalarial activity Tvůrce(i) Frydrych, Jan (UOCHB-X)
Keough, D. T. (AU)
Chavchich, M. (AU)
Travis, J. (AU)
Dračínský, Martin (UOCHB-X) RID, ORCID
Edstein, M. D. (AU)
Guddat, L. W. (AU)
Hocková, Dana (UOCHB-X) RID, ORCID
Janeba, Zlatko (UOCHB-X) RID, ORCIDČíslo článku 113416 Zdroj.dok. European Journal of Medicinal Chemistry. - : Elsevier - ISSN 0223-5234
Roč. 219, Jul 5 (2021)Poč.str. 18 s. Jazyk dok. eng - angličtina Země vyd. FR - Francie Klíč. slova nucleoside phosphonates ; phosphoroamidate prodrug ; HG(X)PRT ; hypoxanthine-guanine-(xanthine) phosphoribosyltransferase ; Plasmodium falciparum ; Plasmodium vivax Obor OECD Organic chemistry CEP GA19-07707S GA ČR - Grantová agentura ČR Způsob publikování Omezený přístup Institucionální podpora UOCHB-X - RVO:61388963 UT WOS 000646945500006 EID SCOPUS 85104345750 DOI 10.1016/j.ejmech.2021.113416 Anotace Parasites of the Plasmodium genus are unable to produce purine nucleotides de novo and depend completely on the salvage pathway. This fact makes plasmodial hypoxanthine-guanine-(xanthine) phosphoribosyltransferase [HG(X)PRT] a valuable target for development of antimalarial agents. A series of nucleotide analogues was designed, synthesized and evaluated as potential inhibitors of Plasmodium falciparum HGXPRT, P. vivax HGPRT and human HGPRT. These novel nucleoside phosphonates have a pyrrolidine, piperidine or piperazine ring incorporated into the linker connecting the purine base to a phosphonate group(s) and exhibited a broad range of Ki values between 0.15 and 72 μM. The corresponding phosphoramidate prodrugs, able to cross cell membranes, have been synthesized and evaluated in a P. falciparum infected human erythrocyte assay. Of the eight prodrugs evaluated seven exhibited in vitro antimalarial activity with IC50 values within the range of 2.5–12.1 μM. The bis-phosphoramidate prodrug 13a with a mean (SD) IC50 of 2.5 ± 0.7 μM against the chloroquine-resistant P. falciparum W2 strain exhibited low cytotoxicity in the human hepatocellular liver carcinoma (HepG2) and normal human dermal fibroblasts (NHDF) cell lines at a concentration of 100 μM suggesting good selectivity for further structure-activity relationship investigations. Pracoviště Ústav organické chemie a biochemie Kontakt asep@uochb.cas.cz ; Kateřina Šperková, Tel.: 232 002 584 ; Jana Procházková, Tel.: 220 183 418 Rok sběru 2022 Elektronická adresa https://doi.org/10.1016/j.ejmech.2021.113416
Počet záznamů: 1