Heterocycle-peptide hybrid compounds. Aminotriazole-containing agonists ofthe thrombin receptor (PAR-1)

Citation
Df. Mccomsey et al., Heterocycle-peptide hybrid compounds. Aminotriazole-containing agonists ofthe thrombin receptor (PAR-1), BIOORG MED, 9(10), 1999, pp. 1423-1428
Citations number
25
Categorie Soggetti
Chemistry & Analysis
Journal title
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
ISSN journal
0960894X → ACNP
Volume
9
Issue
10
Year of publication
1999
Pages
1423 - 1428
Database
ISI
SICI code
0960-894X(19990517)9:10<1423:HHCAAO>2.0.ZU;2-Q
Abstract
The thrombin receptor PAR-1 is activated by cl-thrombin to stimulate cells, including platelets, through the tethered-ligand sequence SFLLRN. We have discovered a novel series of heterocycle-peptide hybrids comprised of a tri peptide segment, such as Cha-Arg-Phe, and an N-terminal heterocyclic group, many of which behave as full PAR-1 agonists. Certain compounds with an ami notriazole group, such as 4 and 16, are nearly as potent as SFLLRN-NH2, in inducing platelet aggregation. Also, some arylethenoyl "N-capped" compounds , such as 52 and 57, exhibit mixed PAR-1 agonist-antagonist activity. (C) 1 999 Elsevier Science Ltd. All rights reserved.