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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


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
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


Projekti:
0098093
0125003
0119632

Ustanove:
Institut "Ruđer Bošković", Zagreb,
Tekstilno-tehnološki fakultet, Zagreb,
Prirodoslovno-matematički fakultet, Zagreb,
Fakultet kemijskog inženjerstva i tehnologije, Zagreb

Poveznice na cjeloviti tekst rada:

doi dx.doi.org www.sciencedirect.com

Citiraj ovu publikaciju:

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
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)
Raić-Malić, S., Tomašković, L., Mrvoš-Sermek, D., Prugovečki, B., Cetina, M., Grdiša, M., Pavelić, K., Mannschreck, A., Balzarini, J., De Clercq, E. & Mintas, M. (2004) Spirobipyridopyrans, spirobinaphthopyrans, indolinospiropyridopyrans, indolinospironaphthopyrans and indolinospironaphtho-1,4-oxazines: synthesis, study of X-ray crystal structure, antitumoral and antiviral evaluation. Bioorganic & medicinal chemistry, 12 (5), 1037-1045 doi:10.1016/j.bmc.2003.12.010.
@article{article, author = {Rai\'{c}-Mali\'{c}, Silvana and Toma\v{s}kovi\'{c}, Linda and Mrvo\v{s}-Sermek, Draginja and Prugove\v{c}ki, Biserka and Cetina, Mario and Grdi\v{s}a, Mira and Paveli\'{c}, Kre\v{s}imir and Mannschreck, Albrecht and Balzarini, Jan and De Clercq, Erik and Mintas, Mladen}, year = {2004}, pages = {1037-1045}, DOI = {10.1016/j.bmc.2003.12.010}, keywords = {spiropyrans, 1H and 13C NMR spectra, single crystal X-ray analysis, cytostatic activities, antiviral activities}, journal = {Bioorganic and medicinal chemistry}, doi = {10.1016/j.bmc.2003.12.010}, volume = {12}, number = {5}, issn = {0968-0896}, title = {Spirobipyridopyrans, spirobinaphthopyrans, indolinospiropyridopyrans, indolinospironaphthopyrans and indolinospironaphtho-1,4-oxazines: synthesis, study of X-ray crystal structure, antitumoral and antiviral evaluation}, keyword = {spiropyrans, 1H and 13C NMR spectra, single crystal X-ray analysis, cytostatic activities, antiviral activities} }
@article{article, author = {Rai\'{c}-Mali\'{c}, Silvana and Toma\v{s}kovi\'{c}, Linda and Mrvo\v{s}-Sermek, Draginja and Prugove\v{c}ki, Biserka and Cetina, Mario and Grdi\v{s}a, Mira and Paveli\'{c}, Kre\v{s}imir and Mannschreck, Albrecht and Balzarini, Jan and De Clercq, Erik and Mintas, Mladen}, year = {2004}, pages = {1037-1045}, DOI = {10.1016/j.bmc.2003.12.010}, keywords = {spiropyrans, 1H and 13C NMR spectra, single crystal X-ray analysis, cytostatic activities, antiviral activities}, journal = {Bioorganic and medicinal chemistry}, doi = {10.1016/j.bmc.2003.12.010}, volume = {12}, number = {5}, issn = {0968-0896}, title = {Spirobipyridopyrans, spirobinaphthopyrans, indolinospiropyridopyrans, indolinospironaphthopyrans and indolinospironaphtho-1,4-oxazines: synthesis, study of X-ray crystal structure, antitumoral and antiviral evaluation}, keyword = {spiropyrans, 1H and 13C NMR spectra, single crystal X-ray analysis, cytostatic activities, antiviral activities} }

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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  • CA Search (Chemical Abstracts)


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