A Modular Synthesis of an Amphiphilic Oligoaryl-based ApoA1 Mimetic as a Potential Drug Carrier

Patrick Simon Dobrounig, Rolf Breinbauer

Publikation: KonferenzbeitragPosterBegutachtung


Apolipoprotein A1 (apoA1), the largest protein of the high density lipoprotein (HDL), has attracted interest for targeted drug delivery.1 Inspired by the structural elements of already existing peptide-based apoA1 mimetics and apoA1 itself, we have designed potential apoA1 mimetics based on an oligoaryl scaffold.2,3 To allow a flexible and modular synthesis of apoA1 mimetics, building blocks were synthesized with a benzene core unit featuring two leaving groups in 1,4-arrangement differing in their reactivity to allow chemoselective borylation and subsequent oligomerization via iterative Pd-catalyzed cross coupling.4 These building blocks are equipped with side chains mimicking on one side the corresponding polar amino acid (Lys, Glu) and on the other side the lipophillic phenylalanine. With this building blocks in hand amphiphillic oligoaryls with an overall low net charge can be synthesized, which will be subsequently tested towards their ability of selectively transporting HDL incorporated small interfering RNA (siRNA) to Scavenger Receptor B1 expressing cells.

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PublikationsstatusVeröffentlicht - 28 Juni 2016
VeranstaltungTetrahedron Symposium - Barcelona, Barcelona, Spanien
Dauer: 28 Juni 20161 Juli 2016


KonferenzTetrahedron Symposium

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