Disrupting the PCSK9/LDLR protein–protein interaction by an imidazole-based minimalist peptidomimetic
Author:
Affiliation:
1. Dipartimento di Chimica
2. Università degli Studi di Milano
3. 20133 Milano
4. Italy
5. Dipartimento di Scienze della Vita
6. Dipartimento di Scienze Farmaceutiche
Abstract
We report on a tetraimidazole-based β-strand minimalist peptidomimetic as a novel inhibitor of LDLR–PCSK9 protein–protein interaction, a promising target for hypercholesterolemia.
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2016/OB/C6OB01642A
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