Pregled bibliografske jedinice broj: 953240
Insights into biological activity of SAHAquines, hybrids based on SAHA and aminoquinoline motifs
Insights into biological activity of SAHAquines, hybrids based on SAHA and aminoquinoline motifs // EFMC International Symposium on Medicinal Chemistry : Book of Abstracts
Ljubljana, Slovenija, 2018. str. 335-335 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 953240 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Insights into biological activity of SAHAquines, hybrids based on SAHA and aminoquinoline motifs
Autori
Beus, Maja ; Rajić, Zrinka ; Mlinarić, Zvonimir ; Antunović, Maja ; Marijanović, Inga ; Fontinha, Diana ; Prudencio, Miguel ; Held, Jana ; Vlainić, Josipa ; Kosalec, Ivan ; Schols, Dominique ; Zorc, Branka
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
EFMC International Symposium on Medicinal Chemistry : Book of Abstracts
/ - , 2018, 335-335
Skup
EFMC International Symposium on Medicinal Chemistry 2018
Mjesto i datum
Ljubljana, Slovenija, 02.09.2018. - 06.09.2018
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
primaquine ; aminoquinoline ; SAHA ; biological activity
Sažetak
SAHAquines represent hybrid drugs, developed as a combination of SAHA, an anticancer drug with weak antiplasmodial activity, and an antiplasmodial agent bearing 8-aminoquinoline or 4-aminoquinoline motifs with low anticancer activity, i.e. primaquine (PQ), chloroquine (CQ) or mefloquine (MQ). Two generations of SAHAquines were designed, prepared and biologically evaluated. In the 1st generation SAHA motif was combined with PQ. The designed hybrid drugs differ in linker length/type and/or functional groups: compounds 1 are esters, 2 are carboxylic acids, 4 are unsubstituted and 3 and 5 are O-benzyl and O- methyl substituted hydroxamic acids. 2nd generation of SAHAquines, fumaric acid diamides 6−8 were designed as Michael acceptors. One of the amide bonds was achieved with a terminal amino group of PQ, CQ or MQ, while the other amide bond was realized with halogen anilines. To fully explore the biological potential of SAHAquines, an extensive screening was performed: antiproliferative (a panel of cancer cell lines), antiplasmodial (both erythrocytic and hepatic stages), antibacterial (G(+) and G(−) bacteria and several Mycobacterium species) and antiviral (a series of DNA and RNA viruses) activity was evaluated. So far, results have shown that SAHAquines of the 1st generation exert antiproliferative and antiplasmodial activity on both erythrocytic and hepatic stages, while the 2nd generation SAHAquines exhibit significant biofilm eradication capacity. Further testing is in progress.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Biologija, Farmacija
POVEZANOST RADA
Projekti:
IP-2014-09-1501 - Dizajniranje, sinteza i evaluacija derivata primakina, vorinostata i sorafeniba kao potencijalnih citostatika (PVSderivatives) (HRZZ - 2014-09) ( CroRIS)
Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb,
Institut "Ruđer Bošković", Zagreb,
Prirodoslovno-matematički fakultet, Zagreb
Profili:
Josipa Vlainić
(autor)
Branka Zorc
(autor)
Maja Antunović
(autor)
Maja Beus
(autor)
Ivan Kosalec
(autor)
Zrinka Rajić
(autor)
Inga Urlić
(autor)
Zvonimir Mlinarić
(autor)