Pregled bibliografske jedinice broj: 778490
Synthesis, QSAR, and molecular dynamics simulation of amidino-substituted benzimidazoles as dipeptidyl peptidase III inhibitors
Synthesis, QSAR, and molecular dynamics simulation of amidino-substituted benzimidazoles as dipeptidyl peptidase III inhibitors // Acta chimica Slovenica, 62 (2015), 4; 867-878 doi:10.17344/acsi.2015.1605 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 778490 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Synthesis, QSAR, and molecular dynamics simulation of amidino-substituted benzimidazoles as dipeptidyl peptidase III inhibitors
Autori
Rastija, Vesna ; Agić, Dejan ; Tomić, Sanja ; Nikolić, Sonja ; Hranjec, Marijana ; Karminski-Zamola, Grace ; Abramić, Marija
Izvornik
Acta chimica Slovenica (1318-0207) 62
(2015), 4;
867-878
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
molecular modeling ; dipeptidyl peptidase III ; benzimidazole derivatives
Sažetak
A molecular modeling study has been performed on a series of 16 benzimidazole-based inhibitors of human dipeptidyl peptidase III (DPP III). Eight of these were novel compounds synthesized in excellent yields using green chemistry approach. This study aims at elucidating the structural features of benzimidazole derivatives required for the antagonism of human DPP III activity using Quantitative Structure-Activity Relationship (QSAR) analysis, and at understanding the mechanism of one of the most potent inhibitor bindings into the active site of this enzyme, namely by molecular dynamics (MD) simulations. The best model obtained includes S3K and RDF045m descriptors, which have explained 89.4 % of inhibitory activity. The depicted moiety for the strong inhibition activity matches the structure of the most potent compound. MD simulation has revealed the importance of imidazolinyl and phenyl groups in the mechanism of binding into the active site of human DPP III.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Biologija, Farmacija
POVEZANOST RADA
Projekti:
MZOS-098-1191344-2860 - Proučavanje biomakromolekula računalnim metodama i razvoj novih algoritama (Tomić, Sanja, MZOS ) ( CroRIS)
MZOS-098-1191344-2938 - Molekularna enzimologija i proteinske interakcije hidrolaza (Abramić, Marija, MZOS ) ( CroRIS)
MZOS-125-0982464-1356 - Novi heterocikli kao antitumorski i antivirusni (pametni) lijekovi (Hranjec, Marijana, MZOS ) ( CroRIS)
Ustanove:
Fakultet agrobiotehničkih znanosti Osijek,
Institut "Ruđer Bošković", Zagreb,
Fakultet kemijskog inženjerstva i tehnologije, Zagreb
Profili:
Marijana Hranjec
(autor)
Sonja Nikolić
(autor)
Dejan Agić
(autor)
Marija Abramić
(autor)
Sanja Tomić
(autor)
Vesna Rastija
(autor)
Grace Karminski-Zamola
(autor)
Poveznice na cjeloviti tekst rada:
Pristup cjelovitom tekstu rada doi fulir.irb.hr fulir.irb.hr journals.matheo.si dx.doi.orgCitiraj 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)