Pregled bibliografske jedinice broj: 521385
Benzylidene-bis-(4-Hydroxycoumarin) and Benzopyranocoumarin Derivatives: Synthesis, 1H/13C NMR Conformational and X-ray Crystal Structure Studies and in vitro Antiviral Activity Evaluations
Benzylidene-bis-(4-Hydroxycoumarin) and Benzopyranocoumarin Derivatives: Synthesis, 1H/13C NMR Conformational and X-ray Crystal Structure Studies and in vitro Antiviral Activity Evaluations // Molecules, 16 (2011), 7; 6023-6040 doi:10.3390/molecules16076023 (međunarodna recenzija, članak, znanstveni)
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Naslov
Benzylidene-bis-(4-Hydroxycoumarin) and Benzopyranocoumarin Derivatives: Synthesis, 1H/13C NMR Conformational and X-ray Crystal Structure Studies and in vitro Antiviral Activity Evaluations
Autori
Završnik, Davorka ; Muratović, Samija ; Makuc, Damjan ; Plavec, Janez ; Cetina, Mario ; Nagl, Ante ; De Clercq, Erik ; Balzarini, Jan ; Mintas, Mladen
Izvornik
Molecules (1420-3049) 16
(2011), 7;
6023-6040
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
4-hydroxycoumarin; benzopyranocoumarin; antiviral activity; 1H/13C NMR conformational study; X-ray diffraction
Sažetak
We report on the synthesis of 4-hydroxycoumarin dimers bearing an aryl substituent on the central linker (1-15) and fused benzopyranocoumarin derivatives (16-20) and on their in vitro broad anti-DNA and RNA virus activity evaluations. The chemical identities and structure of compounds (1-20) were deduced from their homo- and heteronuclear NMR measurements whereas the conformational properties of 5, 14 and 20 were assessed by the use of 1D difference NOE enhancements. Unequivocal proof of the stereostructure of compounds 7, 9, 16 and 18 was obtained by single crystal X-ray diffraction method. The X-ray crystal structure analysis revealed that two 4-hydroxycoumarin moieties in 4-trifluoromethylphenyl (7) and 2-nitrophenyl (9) derivatives are intramolecularly hydrogen-bonded between hydroxyl and carbonyl oxygen atoms. Consequently, the compounds 7 and 9 adopt conformations in which two 4-hydroxycoumarin moieties are anti-disposed. Antiviral activity evaluation results indicated that the 4-bromobenzylidene derivative of bis-(4-hydroxycoumarin) (3) possesses inhibitory activity against HSV-1 (KOS), HSV-2 (G), vaccinia virus and HSV-1 TK- KOS (ACVr) at a concentration of 9-12 μM and at a minimum cytotoxic concentration (MCC) greater than 20 μM. Compounds 4-6, 8, and 20 were active against feline herpes virus (50% effective concentration, EC50 = 5-8.1 μM), that is at a 4-7-fold lower concentration than the MCC.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
119-1193079-3069 - Novi organski i koordinacijski spojevi - sinteza i suodnos struktura-svojstvo (Kaitner, Branko, MZOS ) ( CroRIS)
125-0982464-2922 - RAZVOJ NOVIH PROLIJEKOVA I LIJEKOVA PROTIV VIRUSA I RAKA (Mintas, Mladen, MZOS ) ( CroRIS)
Ustanove:
Tekstilno-tehnološki fakultet, Zagreb,
Prirodoslovno-matematički fakultet, Zagreb,
Fakultet kemijskog inženjerstva i tehnologije, Zagreb
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE