Pregled bibliografske jedinice broj: 1002604
Conformational Analysis and Biological Evaluation of Ferrocene Peptidomimetics
Conformational Analysis and Biological Evaluation of Ferrocene Peptidomimetics // 2nd International Conference on Biotechnology
Valencia, Španjolska, 2019. str. 2-2 (pozvano predavanje, recenziran, sažetak, znanstveni)
CROSBI ID: 1002604 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Conformational Analysis and Biological Evaluation of Ferrocene Peptidomimetics
Autori
Barišić, Lidija ; Kovačević, Monika ; Radošević, Kristina
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
2nd International Conference on Biotechnology
/ - , 2019, 2-2
Skup
2nd International Conference on Biotechnology
Mjesto i datum
Valencia, Španjolska, 15.04.2019. - 16.04.2019
Vrsta sudjelovanja
Pozvano predavanje
Vrsta recenzije
Recenziran
Ključne riječi
ferrocene, peptidomimetic, conformational analysis, biological activity
(ferrocene, peptidomimetic, conformational analysis, biological activit)
Sažetak
The low metabolic stability as well as poor absorption and undesired side effects caused by interaction of conformationally changeable peptides with diverse receptors represent the major obstacles to their pharmaceutical application. The development of peptidomimetics with rigidified conformation and improved biostability has proven as an efficient step towards overcoming these drawbacks. One of the strategic approaches to the peptidomimetic design is based on the utilization of small molecular scaffold capable of inducing the secondary structure upon incorporation into peptide backbone. In this respect, 1, 1′-disubstituted ferrocene (Fc) scaffolds, equipped with hydrogen bonding functionalities, have been employed to nucleate turns and -sheet-like structures.1 The previous results2 obtained on peptides I composed of ‒NH‒Fc‒CO‒ scaffold and Pro confirmed the presence of γ-turn, realized through intrachain hydrogen bonding. Their biological evaluation, performed with regard to antiproliferative effect on MCF7 and HeLa cell line, has been demonstrated no or rather modest cytotoxic effect. In order to improve the biological activity of the ferrocene conjugates with Pro I, we have synthesized their higher homologues II with inserted Ala unit between ferrocene unit and Pro. This structural modification was found to influence the conformational pattern of the peptides II, but the enhanced cytotoxicity was not observed.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Biotehnologija
POVEZANOST RADA
Projekti:
IHRZZ-IP-2014-09-7899
HRZZ-IP-2016-06-3848 - Primjena proteinskih hidrolizata iz pogača lana i konoplje u medijima za uzgoj životinjskih stanica (HYDRO PEP CELL) (Gaurina Srček, Višnja, HRZZ - 2016-06) ( CroRIS)
Ustanove:
Prehrambeno-biotehnološki fakultet, Zagreb