Peptidomimicry with C2 -Symmetric Oligourea Derivatives of 1,2-Diaminocyclohexane and 1,2-Diphenyl-1,2-diaminoethane: Chirality and Chain Length-Dependent Conformation-Reference-Cited by-同舟云学术

Peptidomimicry with C2 -Symmetric Oligourea Derivatives of 1,2-Diaminocyclohexane and 1,2-Diphenyl-1,2-diaminoethane: Chirality and Chain Length-Dependent Conformation

Published:2018-10-24 Issue:39 Volume:3 Page:11035-11041
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Yue Pengyun¹,Peng Siqing¹,Parkin Sean²,Li Tonglei³,Yu Faquan¹,Long Sihui¹^ORCID

Affiliation:

1. Key Laboratory for Green Chemical Process of Ministry of Education, Hubei Key Laboratory of Novel Reactor and Green Chemical Technology; School of Chemical Engineering and Pharmacy, Wuhan Institute of Technology, 206 1 Rd Optics Valley, East Lake New Technology Development District, Wuhan, Hubei; 430205 China

2. Department of Chemistry; University of Kentucky, Lexington, Kentucky; 40506 USA

3. Department of Industrial and Physical Pharmacy; Purdue University, West Lafayette; Indiana 47907 U.S.A

Funder

National Science Foundation of Hubei Province

Crystallography at UK

Publisher

Wiley

Subject

General Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/slct.201801900/fullpdf

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3. Electrostatic versus Steric Effects in Peptidomimicry: Synthesis and Secondary Structure Analysis of Gramicidin S Analogues with (E)-Alkene Peptide Isosteres

4. Fluorine Containing Molecules for Peptidomimicry: A Chemical Act to Modulate Enzymatic Activity

5. Examination of a Structural Model of Peptidomimicry by Cyclic Acyldepsipeptide Antibiotics in Their Interaction with the ClpP Peptidase