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Pregled bibliografske jedinice broj: 662467

Synthesis and Anti-inflammatory Activity of Novel Furochromenes


Jivkov Elenkov, Ivaylo; Hrvačić, Boška; Marković, Stribor; Mesić, Milan; Čempuh Klonkay, Andreja; Lerman, Lidija; Filipović Sučić, Anita; Vujasinović, Ines; Bošnjak, Berislav; Brajša, Karmen et al.
Synthesis and Anti-inflammatory Activity of Novel Furochromenes // Croatica chemica acta, 86 (2013), 3; 253-264 doi:10.5562/cca2240 (međunarodna recenzija, članak, znanstveni)


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Naslov
Synthesis and Anti-inflammatory Activity of Novel Furochromenes

Autori
Jivkov Elenkov, Ivaylo ; Hrvačić, Boška ; Marković, Stribor ; Mesić, Milan ; Čempuh Klonkay, Andreja ; Lerman, Lidija ; Filipović Sučić, Anita ; Vujasinović, Ines ; Bošnjak, Berislav ; Brajša, Karmen ; Žiher, Dinko ; Košutić Hulita, Nada ; Malnar, Ivica

Izvornik
Croatica chemica acta (0011-1643) 86 (2013), 3; 253-264

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
furochromenes; 4-hydroxycoumarins; mast cell degranulation; leukotriene B4; antiinflammatory activity; ear edema

Sažetak
A series of variously substituted furochromenes, hemiacetals 2, acetals 3, and rearranged compounds4, were synthesized from variously substituted 4-hydroxycoumarins and evaluated in several in vitro assays, inhibition of mast cell degranulation induced by the activation of Fcε receptor type I or calcium ionophore and leukotriene B4 (LTB4) inhibition. The most active derivatives, 3p and 4p (8-iso-propyl substitution in coumarin ring) and 3r (5-methyl-8-chloro substitution), showed significant inhibition of mast cell degranulation (Fctriggered) and LTB4, and exhibited significant local anti-inflammatory activity in PMA induced ear edema in CD1 mice, with potency equal (compounds 3p and 4p) or better (compound 3r) in comparison with zileuton, a reference drug used. It might be a promising direction for developing novel drugs as potential agents for the treatment of allergies and other inflammatory diseases

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Ustanove:
Imunološki zavod d.d.,
PLIVA HRVATSKA d.o.o.,
Fidelta d.o.o.

Poveznice na cjeloviti tekst rada:

doi Hrčak

Citiraj ovu publikaciju:

Jivkov Elenkov, Ivaylo; Hrvačić, Boška; Marković, Stribor; Mesić, Milan; Čempuh Klonkay, Andreja; Lerman, Lidija; Filipović Sučić, Anita; Vujasinović, Ines; Bošnjak, Berislav; Brajša, Karmen et al.
Synthesis and Anti-inflammatory Activity of Novel Furochromenes // Croatica chemica acta, 86 (2013), 3; 253-264 doi:10.5562/cca2240 (međunarodna recenzija, članak, znanstveni)
Jivkov Elenkov, I., Hrvačić, B., Marković, S., Mesić, M., Čempuh Klonkay, A., Lerman, L., Filipović Sučić, A., Vujasinović, I., Bošnjak, B. & Brajša, K. (2013) Synthesis and Anti-inflammatory Activity of Novel Furochromenes. Croatica chemica acta, 86 (3), 253-264 doi:10.5562/cca2240.
@article{article, year = {2013}, pages = {253-264}, DOI = {10.5562/cca2240}, keywords = {furochromenes, 4-hydroxycoumarins, mast cell degranulation, leukotriene B4, antiinflammatory activity, ear edema}, journal = {Croatica chemica acta}, doi = {10.5562/cca2240}, volume = {86}, number = {3}, issn = {0011-1643}, title = {Synthesis and Anti-inflammatory Activity of Novel Furochromenes}, keyword = {furochromenes, 4-hydroxycoumarins, mast cell degranulation, leukotriene B4, antiinflammatory activity, ear edema} }
@article{article, year = {2013}, pages = {253-264}, DOI = {10.5562/cca2240}, keywords = {furochromenes, 4-hydroxycoumarins, mast cell degranulation, leukotriene B4, antiinflammatory activity, ear edema}, journal = {Croatica chemica acta}, doi = {10.5562/cca2240}, volume = {86}, number = {3}, issn = {0011-1643}, title = {Synthesis and Anti-inflammatory Activity of Novel Furochromenes}, keyword = {furochromenes, 4-hydroxycoumarins, mast cell degranulation, leukotriene B4, antiinflammatory activity, ear edema} }

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


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