Design, Synthesis, and Evaluation of New Hybrid Derivatives of 5,6-Dihydro-4
5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-2-one
anticoagulant activity
blood coagulation
dual activity
factor XIa
factor Xa
inhibitor
molecular docking
thiazole
thrombin
Journal
Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009
Informations de publication
Date de publication:
11 Jan 2024
11 Jan 2024
Historique:
received:
30
10
2023
revised:
29
12
2023
accepted:
08
01
2024
medline:
23
1
2024
pubmed:
23
1
2024
entrez:
23
1
2024
Statut:
epublish
Résumé
Cardiovascular diseases caused by blood coagulation system disorders are one of the leading causes of morbidity and mortality in the world. Research shows that blood clotting factors are involved in these thrombotic processes. Among them, factor Xa occupies a key position in the blood coagulation cascade. Another coagulation factor, XIa, is also a promising target because its inhibition can suppress thrombosis with a limited contribution to normal hemostasis. In this regard, the development of dual inhibitors as new generation anticoagulants is an urgent problem. Here we report the synthesis and evaluation of novel potential dual inhibitors of coagulation factors Xa and XIa. Based on the principles of molecular design, we selected a series of compounds that combine in their structure fragments of pyrrolo[3,2,1-
Identifiants
pubmed: 38257286
pii: molecules29020373
doi: 10.3390/molecules29020373
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Federal Service for Supervision of Consumer Protection
ID : GZ 43/21