Pregled bibliografske jedinice broj: 146386
Spirobipyridopyrans, spirobinaphthopyrans, indolinospiropyridopyrans, indolinospironaphthopyrans and indolinospironaphtho-1,4-oxazines: synthesis, study of X-ray crystal structure, antitumoral and antiviral evaluation
Spirobipyridopyrans, spirobinaphthopyrans, indolinospiropyridopyrans, indolinospironaphthopyrans and indolinospironaphtho-1,4-oxazines: synthesis, study of X-ray crystal structure, antitumoral and antiviral evaluation // Bioorganic & medicinal chemistry, 12 (2004), 5; 1037-1045 doi:10.1016/j.bmc.2003.12.010 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 146386 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Spirobipyridopyrans, spirobinaphthopyrans, indolinospiropyridopyrans, indolinospironaphthopyrans and indolinospironaphtho-1,4-oxazines: synthesis, study of X-ray crystal structure, antitumoral and antiviral evaluation
Autori
Raić-Malić, Silvana ; Tomašković, Linda ; Mrvoš-Sermek, Draginja ; Prugovečki, Biserka ; Cetina, Mario ; Grdiša, Mira ; Pavelić, Krešimir ; Mannschreck, Albrecht ; Balzarini, Jan ; De Clercq, Erik ; Mintas, Mladen
Izvornik
Bioorganic & medicinal chemistry (0968-0896) 12
(2004), 5;
1037-1045
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
spiropyrans ; 1H and 13C NMR spectra ; single crystal X-ray analysis ; cytostatic activities ; antiviral activities
Sažetak
The novel racemic indolinospirobenzopyrans (5- 7), indolinospironaphthopyrans (11-14) and indolinospironaphtho-1, 4-oxazine (17) were synthesized by an aldol type of condensation of 1', 3', 3'-trimethyl-2'-methyleneindoline and its 5-substituted derivatives with an appropriately substituted hydroxybenzaldehyde, hydroxynaphthaldehyde or nitrosonaphthol. An unequivocal proof of the stereostructures of 9 and 17 was obtained by the single-crystal X-ray diffraction method. A substituted indoline ring and the benzopyran ring in 9 and the naphtho-1, 4-oxazine moiety in 17 are interconnected via the common chiral atom and positioned almost perpendicularly to each other. The five- membered 2, 3-dihydropyrrolo moiety of the indoline ring adopts an envelope conformation in both structures. Of all the compounds of this series, indolinospirobenzopyran (9), containing a methoxy group at the position 6 of the benzopyran ring, exhibited the most pronounced inhibitory effects on the growth of human CEM (IC50: 0.68 mg/ml) and Molt4/C8 (IC50: 0.71 mg/ml) cells. Spirobipyridopyran (1) inhibited specifically the growth of human melanoma (HBL) (IC50: 0.9 mM) cells but not the growth of normal fibroblasts (WI38). The best cytostatic activity was achieved with the compounds 8, 9 and 10, from the class of indolinospirobenzopyrans. The indolinospirobenzopyrans 4, 6-8, 10 and the indolinospironaphtho-1, 4-oxazine 16 showed, albeit modest, selectivity as antiviral agents against varicella-zoster virus (VZV) and/or cytomegalovirus (CMV) (EC50 within the concentration range of 0.4-4 µ ; ; ; g/ml).
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Ustanove:
Institut "Ruđer Bošković", Zagreb,
Tekstilno-tehnološki fakultet, Zagreb,
Prirodoslovno-matematički fakultet, Zagreb,
Fakultet kemijskog inženjerstva i tehnologije, Zagreb
Profili:
Linda Tomašković
(autor)
Mladen Mintas
(autor)
Mirica Grdiša
(autor)
Biserka Prugovečki
(autor)
Krešimir Pavelić
(autor)
Silvana Raić-Malić
(autor)
Draginja Mrvoš-Sermek
(autor)
Mario Cetina
(autor)
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
Uključenost u ostale bibliografske baze podataka::
- CA Search (Chemical Abstracts)