7625-59-4Relevant articles and documents
Gram-Scale Synthesis of a Hexapeptide by Fragment Coupling in a Ball Mill
Lamaty, Frédéric,Métro, Thomas-Xavier,Martinez, Jean,Rguioueg, Nadia,Subra, Gilles,Yeboue, Yves
supporting information, (2021/09/20)
Synthesis of long peptides is generally considered as a challenge to peptide chemists, in addition to producing significant amounts of toxic waste, such as DMF. Here we show that using solvent-less methods, such as ball milling, enabled the production of
Synthesis and Biological Evaluation of Analogues of Pro-Leu-Gly-NH2 Modified at the Leucyl Residue
Johnson, Rodney L.,Bontems, Roger J.,Yang, Kaipeen E.,Mishra, Ram K.
, p. 1828 - 1832 (2007/10/02)
A series of analogues of Pro-Leu-Gly-NH2 (PLG) in which the leucine residue has been replaced with the aliphatic amino acids L-isoleucine, L-2-aminohexanoic acid (Ahx), L-2-aminopentanoic acid, and L-2-aminobutanoic acid and the aromatic amino acids L-phenylalanine, L-phenylglycine, L- and D-2-amino-4-phenylbutanoic acid, L-O-methyltyrosine, and L-4-nitrophenylalanine have been synthesized.These analogues were tested for their ability to enhance the binding of the dopamine receptor agonist 2-amino-6,7-dihydroxy-1,2,3,4-tetrahydronaphthalene (ADTN) to striatal dopamine receptors.Two of the abov e analogues, Pro-Ahx-Gly-NH2 (3) and Pro-Phe-Gly-NH2 (6), showed significant activity in this assay system.Pro-Ahx-Gly-NH2 produced a 16percent enhancement of ADTN binding at 0.1 μM, while Pro-Phe-Gly-NH2 enhanced the binding of ADTN by 31percent at a concentration of 1 μM.
Oligopeptides of β-carboline-3-carboxylic acid - Synthesis and benzodiazepine receptor affinity
Lippke,Muller,Schunack
, p. 145 - 153 (2007/10/02)
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