Pregled bibliografske jedinice broj: 1159658
Synthesis of ferrocene ester derivatives of desmuramyl peptide
Synthesis of ferrocene ester derivatives of desmuramyl peptide // Book of Abstract, XXVI EFMC International Symposium on Medicinal Chemistry, Virtual Event
online, 2021. str. 425-425 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 1159658 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Synthesis of ferrocene ester derivatives of
desmuramyl peptide
Autori
Petrović Peroković, Vesna ; Car, Željka ; Ribić, Rosana ; Kovačević, Monika ; Barišić, Lidija
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Book of Abstract, XXVI EFMC International Symposium on Medicinal Chemistry, Virtual Event
/ - , 2021, 425-425
Skup
XXVI EFMC International Symposium on Medicinal Chemistry
Mjesto i datum
Online, 29.08.2021. - 02.09.2021
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
adjuvant activity, desmuramyl peptide, ester bond, ferrocene alcohols
Sažetak
Derivatives of muramyl dipeptide (MDP), a well- known peptidoglycan fragment, have been extensively studied as possible adjuvants for human and animal vaccines. [1] MDP analogues without the N- acetylmuramyl moiety are called desmuramyl peptides (DMP). Structure-activity studies of the MDP derivatives and their analogues suggest that L-Ala- D-isoGln pharmacophore is essential for the immunostimulatory properties and that the introduction of lipophilic substituent can increase its adjuvant activity. In our previous research we reported the synthesis and immunostimulatory activity of DMP with an adamantane group on L-Ala-D-iGln fragment. [2] Furthermore, we prepared and biologically evaluated mannosylated adamantane derivatives of DMP which showed enhanced immunostimulatory activity compared to compounds without the mannose subunit. The acitivity of such compounds was additionally positively influenced by the glycolyl spacer between mannose unit and desmuramyl peptide. [3] The two bioorganometallic analogues of MDP bearing lipophilic ferrocene subunit were also previously synthesized by our group. [4] In this work we described the synthesis of novel class of DMP derivatives in which lipophilic ferrocene unit was introduced at C-terminus of L- Ala-D-iGln via ester bond, followed by mannosylation of N-terminus through glycolyl spacer. Furthermore, alkyl spacers of different length will also be introduced between desmuramyl peptide and ferrocene unit to further increase lipophilicity of the synthesized compounds. This work has been fully supported by Croatian Science Foundation under the project IP-2020-02- 9162. 1. R. Ribić, M. Paurević, S. Tomić, Croat. Chem. Acta 92 (2019) 153-161. 2. (a) R. Ribić, L. Habjanec, B. Vranešić, R. Frkanec, S. Tomić, Chem. Biodivers. 9 (2012) 777- 788., (b) R. Ribić, L. Habjanec, R. Frkanec, B. Vranešić, S. Tomić, Chem. Biodivers. 9 (2012) 1373- 1381. 3. R. Ribić, R. Stojković, L. Milković, M. Antica, M. Cigler, S. Tomić, Beilstein J. Org. Chem. 15 (2019) 1805- 1814. 4. L. Barišić, M. Roščić, M. Kovačević, M. Čakić Semenčić, Š. Horvat, V. Rapić, Carbohydr. Res. 346 (2011) 678-684.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
--IP-2020-02-9162 - Ferocenski analozi biomolekula: strukturna karakterizacija i biološka evaluacija (FER-AN-BIOMOL) (Barišić, Lidija) ( CroRIS)
Ustanove:
Prehrambeno-biotehnološki fakultet, Zagreb,
Prirodoslovno-matematički fakultet, Zagreb,
Sveučilište Sjever, Koprivnica
Profili:
Rosana Ribić
(autor)
Vesna Petrović-Peroković
(autor)
Lidija Barišić
(autor)
Monika Kovačević
(autor)
Željka Car
(autor)