Abstract
A series of substituted [1]benzothieno [2,3-b]pyrazines, structurally related to caroverine, was synthesized. Some of these compounds showed an appreciable inhibition towards KCl induced contractions on isolated rat aortic rings, and a lower potency towards negative inotropic activity tested on isolated guinea pig atrium.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Aorta / drug effects
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Aorta / physiology
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Calcium Channel Blockers / chemical synthesis*
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Calcium Channel Blockers / pharmacology
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In Vitro Techniques
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Potassium Chloride / pharmacology
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Pyrazines / chemical synthesis*
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Pyrazines / pharmacology
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Quinoxalines / chemical synthesis*
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Quinoxalines / pharmacology
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Rats
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Rats, Wistar
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Structure-Activity Relationship
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Vasoconstriction / drug effects*
Substances
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Calcium Channel Blockers
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Pyrazines
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Quinoxalines
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Potassium Chloride
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caroverine