Publication:
Design andsynthesis of novelpeptidomimetics for cancer immunotherapy

dc.contributor.authorsCeyda KÖSE;Esra UYSAL;Büşra YAZICI;Zeynep TUĞAY;Sevgi GÜLYÜZ;Onur ALPTÜRK;Özgür YILMAZ;Serap İpek Dingiş BİRGÜL;Hamdullah YANIK;Ece TAVUKÇUOĞLU;Güneş ESENDAĞLI;Atilla AKDEMİR
dc.date.accessioned2022-03-15T16:58:13Z
dc.date.accessioned2026-01-10T20:41:29Z
dc.date.available2022-03-15T16:58:13Z
dc.date.issued2020-09-27
dc.description.abstractTumor cells benefit from some certainsignals, which are referred to as “immune checkpoints”,to escape immune-mediated destruction. With that in mind, it is believed that the blockade of thesepoints, such as programmed cell death Ligand-1 (PD-L1) and programmed cell death 1 (PD-1), can restorean adaptative immune response against tumoral cells.In this study, we have designed and synthesized some novel peptidomimetics with a 2-aminobenzathiazole scaffold, which targetsthe PD-1/PDL-1 pathway. In the viability assay, it was found that these compounds decreased the proliferation of peripheral blood mononuclear cells in the concentration of 10 uM.Overall,ourresults indicate that these novel compounds are potentialcheckpoint inhibitorsforcancer immunotherapy.
dc.identifier.doi10.25135/acg.oc.86.20.09.1802
dc.identifier.issnnull;1307-6175
dc.identifier.urihttps://hdl.handle.net/11424/253404
dc.language.isoeng
dc.relation.ispartofOrganic Communications
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleDesign andsynthesis of novelpeptidomimetics for cancer immunotherapy
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage102
oaire.citation.issue3
oaire.citation.startPage89
oaire.citation.titleOrganic Communications
oaire.citation.volume13

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