Peptides 1998-01-01

Activation of diketopiperazine formation by alkylammonium carboxylate salts and aprotic dipolar protophobic solvents.

S Capasso, L Mazzarella

Index: Peptides 19(2) , 389-91, (1998)

Full Text: HTML

Abstract

Diketopiperazine formation from the N-terminal residues of a peptide chain is accelerated by aprotic dipolar protophobic solvents and catalyzed in organic solvents by alkylammonium carboxylate salts. The t1/2 for the first-order reaction of H-Ala-Pro-NH2 x TFA falls from 20 d in methanol to 3.6 min in acetonitrile containing 0.02 mol dm(-3) triethylammonium acetate; for H-Ala-Ala-NH2 x TFA in the same reaction media t1/2 falls from an unmeasurably long time to 1.3 d.


Related Compounds

Related Articles:

Differential mobility spectrometry of isomeric protonated dipeptides: modifier and field effects on ion mobility and stability.

2011-05-01

[Anal. Chem. 83 , 3470-3476, (2011)]

Infrared spectroscopy of the alanine dipeptide analog in liquid water with DFT-MD. Direct evidence for P(II)/beta conformations.

2010-09-21

[Phys. Chem. Chem. Phys. 12 , 10198-10209, (2010)]

Water-mediated conformations of the alanine dipeptide as revealed by distributed umbrella sampling simulations, quantum mechanics based calculations, and experimental data.

2011-04-28

[J. Phys. Chem. B 115 , 4880-4886, (2011)]

Selectivity of quadruplex DNA stationary phases toward amino acids in homodipeptides and alanyl dipeptides.

2004-05-01

[Electrophoresis 25 , 1230-1236, (2004)]

Manipulation of activity and orientation of membrane-reconstituted di-tripeptide transport protein DtpT of Lactococcus lactis.

1999-01-01

[Mol. Membr. Biol. 16(4) , 297-304, (1999)]

More Articles...