Published January 1, 2013
| Version v1
Journal article
Open
Pyrazole derivatives as inhibitors of arachidonic acid-induced platelet aggregation
Creators
- 1. Gazi Univ, Fac Pharm, Dept Pharmaceut Chem, TR-06330 Ankara, Turkey
- 2. Gazi Univ, Fac Pharm, Dept Biochem, TR-06330 Ankara, Turkey
- 3. Ankara Univ, Fac Sci, Dept Phys, TR-06100 Ankara, Turkey
Description
Antiplatelet drugs are promising therapeutics to intervene with platelet aggregation in arterial thrombosis, most prominently in myocardial infarction and ischemic stroke. Here, we describe the synthesis and structure activity relationships of potent inhibitors of platelet aggregation based on the 1,5-diarylpyrazol-3-carboxamide scaffold. Analogs from this series demonstrated potent anti-aggregatmy activities against arachidonic acid-induced platelet aggregation, as measured by turbidimetric method of Born. 1,5-Diarylpyrazole-3-carboxamides obtained with small-basic amines (7, 8, 50, 51, 61, 62) displayed the strongest activity with IC50 values in low nanomolar range (5.7-83 nM). On the basis of their high potency in cellular environment, these straightforward pyrazole derivatives may possess potential in the design of more potent compounds for intervention with cardiovascular diseases. (C) 2013 Elsevier Masson SAS. All rights reserved.
Files
bib-5a7ffad1-c0df-45ac-b310-009164d35387.txt
Files
(237 Bytes)
| Name | Size | Download all |
|---|---|---|
|
md5:d8df1cd8dbb8aa6d103b7c52542655d6
|
237 Bytes | Preview Download |