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Synthesis and pharmacological evaluation of 2,5-cycloamino-5H-[1]benzopyrano[4,3-d]pyrimidines endowed with in vitro antiplatelet activity.
- Source :
-
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2001 Jun 04; Vol. 11 (11), pp. 1397-400. - Publication Year :
- 2001
-
Abstract
- A series of new 2,5-cycloamino-5H-[1]benzopyrano[4,3-d]pyrimidines 3a-i have been synthesized and tested in vivo for the anti-inflammatory/analgesic/antipyretic effects and in vitro to evaluate the antiplatelet activity on guinea-pig platelet-rich plasma aggregated by collagen, adenosine-5'-diphosphate (ADP) and arachidonic acid (AA). Title compounds were ineffective in vivo; however, the pyrrolidino derivatives 3a and 3c exhibited an antiplatelet activity against all the aggregants differing from that of acetylsalicylic acid (ASA) while the 5-morpholino derivatives 3g-i showed the most potent ASA-like antiplatelet activity.
- Subjects :
- Adenosine Diphosphate metabolism
Analgesics chemical synthesis
Analgesics chemistry
Analgesics pharmacology
Analgesics therapeutic use
Animals
Anti-Inflammatory Agents chemical synthesis
Anti-Inflammatory Agents chemistry
Anti-Inflammatory Agents pharmacology
Anti-Inflammatory Agents therapeutic use
Arachidonic Acid metabolism
Benzopyrans chemistry
Benzopyrans pharmacology
Benzopyrans therapeutic use
Collagen metabolism
Disease Models, Animal
Edema drug therapy
Guinea Pigs
Pain drug therapy
Platelet Aggregation drug effects
Platelet Aggregation Inhibitors chemistry
Platelet Aggregation Inhibitors pharmacology
Platelet Aggregation Inhibitors therapeutic use
Pyrimidines chemistry
Pyrimidines pharmacology
Pyrimidines therapeutic use
Rats
Benzopyrans chemical synthesis
Platelet Aggregation Inhibitors chemical synthesis
Pyrimidines chemical synthesis
Subjects
Details
- Language :
- English
- ISSN :
- 0960-894X
- Volume :
- 11
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry letters
- Publication Type :
- Academic Journal
- Accession number :
- 11378363
- Full Text :
- https://doi.org/10.1016/s0960-894x(01)00221-9