S Capasso, L Mazzarella
Index: Peptides 19(2) , 389-91, (1998)
Full Text: HTML
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.
| Structure | Name/CAS No. | Molecular Formula | Articles |
|---|---|---|---|
![]() |
H-Ala-Pro-OH
CAS:13485-59-1 |
C8H14N2O3 |
|
Differential mobility spectrometry of isomeric protonated di...
2011-05-01 [Anal. Chem. 83 , 3470-3476, (2011)] |
|
Infrared spectroscopy of the alanine dipeptide analog in liq...
2010-09-21 [Phys. Chem. Chem. Phys. 12 , 10198-10209, (2010)] |
|
Water-mediated conformations of the alanine dipeptide as rev...
2011-04-28 [J. Phys. Chem. B 115 , 4880-4886, (2011)] |
|
Selectivity of quadruplex DNA stationary phases toward amino...
2004-05-01 [Electrophoresis 25 , 1230-1236, (2004)] |
|
Manipulation of activity and orientation of membrane-reconst...
1999-01-01 [Mol. Membr. Biol. 16(4) , 297-304, (1999)] |
Home | MSDS/SDS Database Search | Journals | Product Classification | Biologically Active Compounds | Selling Leads | About Us | Disclaimer
Copyright © 2026 ChemSrc All Rights Reserved
