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Benzylidene-bis-(4-Hydroxycoumarin) and Benzopyranocoumarin Derivatives: Synthesis, 1H/13C NMR Conformational and X-ray Crystal Structure Studies and in vitro Antiviral Activity Evaluations


Završnik, Davorka; Muratović, Samija; Makuc, Damjan; Plavec, Janez; Cetina, Mario; Nagl, Ante; De Clercq, Erik; Balzarini, Jan; Mintas, Mladen
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)


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


Projekt / tema
119-1193079-3069 - Novi organski i koordinacijski spojevi - sinteza i suodnos struktura-svojstvo (Branko Kaitner, )
125-0982464-2922 - RAZVOJ NOVIH PROLIJEKOVA I LIJEKOVA PROTIV VIRUSA I RAKA (Mladen Mintas, )

Ustanove
Tekstilno-tehnološki fakultet, Zagreb,
Prirodoslovno-matematički fakultet, Zagreb,
Fakultet kemijskog inženjerstva i tehnologije, Zagreb

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


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