| Identification | Back Directory | [Name]
acetylphenylalanyl-prolyl-boroarginine | [CAS]
130982-43-3 | [Synonyms]
Dup714
Dup-714
Dup 714
acetylphenylalanyl-prolyl-boroarginine
L-Prolinamide, N-acetyl-D-phenylalanyl-N-[(1R)-4-[(aminoiminomethyl)amino]-1-boronobutyl]- | [Molecular Formula]
C21H33BN6O5 | [MOL File]
130982-43-3.mol | [Molecular Weight]
460.33 |
| Hazard Information | Back Directory | [Description]
Dup-714 is a thrombin inhibitor that shows potential for oral treatment of thromboembolic disorders. | [Uses]
DuP 714 is an oral active thrombin inhibitor with the IC50 values of 150 nM aganist thrombin-induced aggregation in washed human platelets. DuP 714 can be used for study of arterial thrombosi[1][2]. | [Definition]
ChEBI: Ac-(D)Phe-Pro-boroArg-OH is a C-terminal boronic acid petide that is N-acetyl-D-phenylalanyl-L-prolyl-L-arginine in which the C-termnal carboxy group has been replaced by a borono (-B(OH)2) group. A thrombin (Factor IIa) inhibitor, thereby acting as an anticoagulant. It has a role as an EC 3.4.21.5 (thrombin) inhibitor and an anticoagulant. It is a C-terminal boronic acid peptide, a member of acetamides and a member of guanidines. It is a conjugate base of an Ac-(D)Phe-Pro-boroArg-OH(1+). | [References]
[1] Reilly TM, et al. Effect of thrombin inhibitors on platelet functions: comparative analysis of DuP 714 and hirudin. Blood Coagul Fibrinolysis. 1992;3(5):513-517. DOI:10.1097/00001721-199210000-00001
[2] Mitchell TJ, et al. Analysis of the thrombin inhibitor DuP 714 by an enzyme-linked immunosorbent assay. Blood Coagul Fibrinolysis. 1994;5(4):517-521. PMID:7841307 |
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