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Literature DB >> 5433911

[Racemization in peptide syntheses].

W König, R Geiger.

Abstract

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Year: 1970 PMID： 5433911 DOI： 10.1002/cber.19701030704

Source DB: PubMed Journal: Chem Ber ISSN： 0009-2940

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8 in total

1. A method for S- and O-palmitoylation of peptides: synthesis of pulmonary surfactant protein-C models.

Authors: E Yousefi-Salakdeh; J Johansson; R Strömberg
Journal: Biochem J Date: 1999-11-01 Impact factor: 3.857

2. The synthesis, kinetic characterization and application of a novel biotinylated affinity label for cathepsin B.

Authors: B Walker; B M Cullen; G Kay; I M Halliday; A McGinty; J Nelson
Journal: Biochem J Date: 1992-04-15 Impact factor: 3.857

3. Nucleophilic carbene and HOAt relay catalysis in an amide bond coupling: an orthogonal peptide bond forming reaction.

Authors: Harit U Vora; Tomislav Rovis
Journal: J Am Chem Soc Date: 2007-10-11 Impact factor: 15.419

4. Accelerated chemical synthesis of peptides and small proteins.

Authors: L P Miranda; P F Alewood
Journal: Proc Natl Acad Sci U S A Date: 1999-02-16 Impact factor: 11.205

5. Effects of L- and D-REKR amino acid-containing peptides on HIV and SIV envelope glycoprotein precursor maturation and HIV and SIV replication.

Authors: Bouchaib Bahbouhi; Nathalie Chazal; Nabil Georges Seidah; Cristina Chiva; Marcelo Kogan; Fernando Albericio; Ernest Giralt; Elmostafa Bahraoui
Journal: Biochem J Date: 2002-09-15 Impact factor: 3.857

[Racemization in peptide syntheses].

1. A method for S- and O-palmitoylation of peptides: synthesis of pulmonary surfactant protein-C models.

2. The synthesis, kinetic characterization and application of a novel biotinylated affinity label for cathepsin B.

3. Nucleophilic carbene and HOAt relay catalysis in an amide bond coupling: an orthogonal peptide bond forming reaction.

4. Accelerated chemical synthesis of peptides and small proteins.

5. Effects of L- and D-REKR amino acid-containing peptides on HIV and SIV envelope glycoprotein precursor maturation and HIV and SIV replication.

6. Specificity studies on enteropeptidase substrates related to the N-terminus of trypsinogen.

7. Inhibition of pepsin by analogues of pepsinogen-(1-12)-peptide with substitutions in the 4-7 sequence region.

8. Unwanted hydrolysis or α/β-peptide bond formation: how long should the rate-limiting coupling step take?