Synthesis and Properties of Gramicidin S Analogs Containing D-Phe–L-Pro–D-Val or L-Phe–L-Pro–D-Val Sequences in Place of D-Phe–L-Pro–L-Val Sequence in the β-Turn Part of the Antibiotic
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/58/2/58_2_531/_pdf
Reference6 articles.
1. Natural homologs of gramicidin S.
2. Appendix 2—Possible molecular models for gramicidin S and their relationship to present ideas of protein structure
3. Studies on Peptide Antibiotic “Gratisin”
4. Comparison of conformation and antimicrobial activity of synthetic analogs of gramicidin S: Stereochemical consideration of the role ofD-phenylalanine in the antibiotic
5. Studies on the β-Turn of Peptides. VII. Syntheses and Antibiotic Activities of Gramicidin S Analogs with L-Pro-L-Asn or L-Pro-D-Ala Sequence at the β-Turn Part
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1. An Ornithine-Free Gramicidin S Analogue Using Norleucine, Cyclo(Val–Nle–Leu–D-Phe–Pro)2, Forms Helically Aligned β-Sheets;Chemical and Pharmaceutical Bulletin;2021-11-01
2. [Leu2]Gramicidin S preserves the structural properties of its parent peptide and forms helically aligned β-sheets;Acta Crystallographica Section C Structural Chemistry;2019-09-06
3. An Overview of the Synthesis of Highly Versatile N-Hydroxysuccinimide Esters;Synthesis;2016-09-23
4. Sequence Inversion and Phenylalanine Surrogates at the β-Turn Enhance the Antibiotic Activity of Gramicidin S;Journal of Medicinal Chemistry;2010-05-27
5. Properties of synthetic analogs of gramicidin S containing L-serine or L-glutamic acid residue in place of L-ornithine residue;International Journal of Peptide and Protein Research;2009-01-12
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