Pregled bibliografske jedinice broj: 897323
Synthesis of multiantenNary mannose derived DESMURAMYL PEPTIDES
synthesis of multiantenNary mannose derived DESMURAMYL PEPTIDES // Book of Abstract, 10th Joint Meeting on Medicinal Chemistry, June 25-28, 2017, Dubrovnik, Croatia / Basarić, Nikola ; Namjesnik, Danijel ; Perković, Ivana ; Stepanić, Višnja (ur.).
Zagreb, 2017. str. 208-208 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 897323 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Synthesis of multiantenNary mannose derived DESMURAMYL PEPTIDES
Autori
Ribić, Rosana ; Paurević, Marija ; Tir, Nora ; Tomić, Srđanka
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Book of Abstract, 10th Joint Meeting on Medicinal Chemistry, June 25-28, 2017, Dubrovnik, Croatia
/ Basarić, Nikola ; Namjesnik, Danijel ; Perković, Ivana ; Stepanić, Višnja - Zagreb, 2017, 208-208
ISBN
978-953-55232-8-4
Skup
10th Joint Meeting on Medicinal Chemistry
Mjesto i datum
Dubrovnik, Hrvatska, 25.06.2017. - 28.06.2017
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
DESMURAMYL PEPTIDES ; ADAMANTYL ; MANNOSYL
Sažetak
Muropeptides are fragments of peptidoglycans, unique polymers that build up the cell wall of bacteria. They are used as immunostimulating compounds (adjuvants). Muramyl dipeptide (MDP), N-acetylmuramyl-L-alanyl-D-isoglutamine, is the smallest structural unit of peptidoglycans showing the immunostimulating activity. Numerous MDP analogues lacking the hydrophilic carbohydrate moiety (desmuramyl peptides) with different groups at C- and N-terminus of the L- Ala-D-isoGln moiety have been synthesized. [1] We have designed and synthesized desmuramyl peptides with incorporated lipophilic adamantyl group and also their mannosylated derivatives. [2, 3] Attached mannose allows the targeting of cell surface receptors recognizing glycans on immune cells while adamantane group facilitates the anchoring of the peptidoglycan ‘cargo’ to the membrane. Synthesized desmuramyl peptides have been encapsulated into liposomes, vehicles often used for the target delivery. In these liposomal formulations adamantane group penetrates into the lipid bilayer while mannose is exposed at the liposome surface and can serve in targeting mannose receptors. [4] In order to improve lectin-carbohydrate binding we are developing methodology for the stereoselective synthesis of di- and tri- antennary mannose derivatives of desmuramyl peptides because increasing of mannose subunits number will enhance strength of overall mannose – lectin interactions.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
HRZZ IP-2014-09-7899 PEPTGLYCOSAR
Ustanove:
Prirodoslovno-matematički fakultet, Zagreb,
Sveučilište J. J. Strossmayera u Osijeku
Profili:
Nora Tir
(autor)
Marija Paurević
(autor)
Rosana Ribić
(autor)
Srđanka Tomić-Pisarović
(autor)