16295-99-1

Basic information

• Product Name: L-piperidine-2-carbonyl-L-leucylglycinamide hydrochloride
• CAS NO: 16295-99-1
• Molecular Weight: 334.846
• Mol File: 16295-99-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: L-piperidine-2-carbonyl-L-leucylglycinamide hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: L-piperidine-2-carbonyl-L-leucylglycinamide hydrochloride(16295-99-1)
• EPA Substance Registry System: L-piperidine-2-carbonyl-L-leucylglycinamide hydrochloride(16295-99-1)

Safety Data

• Hazardous Substances Data: 16295-99-1(Hazardous Substances Data)

Upstream product

• 26250-84-0 (S)-(-)-1-(tert-butoxycarbonyl)-2-piperidinecarboxylic acid 
• 3105-95-1 pipecolinic acid 
• 38173-66-9 HCl_.H-Leu-Gly-NH₂ 
• 103225-09-8 Boc-Pip-Leu-Gly-NH2 

Relevant articles and documents

Synthesis of Pro-Leu-Gly-NH2 Analogues Modified at the Prolyl Residue and Evaluation of Their Effects on the Receptor Binding Activity of the Central Dopamine Receptor Agonist, ADTN

Several analogues of L-prolyl-L-leucylglycinamide (PLG) were synthesized wherein the prolyl residue was replaced with other heterocyclic amino acid residues.Among the analogues synthesized were D-Pro-Leu-Gly-NH2 (2), 3,4-Pro-Leu-Gly-NH2 (7), and D-Δ3,4-Pro-Leu-Gly-NH2 (8).These analogues were tested for their ability to enhance the binding of the agonist 2-amino-6,7-dihydroxy-1,2,3,4-tetrahydronaphthalene to central dopamine receptors.Analogues 2,3, and 5-7 showed activity comparable to that of PLG, while the tripeptides 4 and 8 were found to be inactive.The results show that the N-terminal prolyl residue of PLG is not essential requirement for this tripeptide's ability to modulate dopamine receptors.