Abstract
A new series of 4-amino-6-methylthio-1H-pyrazolo[3,4-d]pyrimidines (2a-m) bearing the 2-chloro-2-phenylethyl chain at the N1 position, has been synthesized. The affinity of these compounds for A1 adenosine receptor (A1AR) was measured. The compounds showed poor affinity. A more interesting result was obtained by 2a, 2d, 2g, which demonstrated inhibitory activity on cell proliferation of the A-431 cell line stimulated by epithelial growth factor (EGF) and on EGF receptor tyrosine kinase (EGFR-TK) phosphorylation.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adenosine A1 Receptor Antagonists
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Cell Division / drug effects
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Cell Line, Tumor
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Drug Screening Assays, Antitumor / methods
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Epidermal Growth Factor / antagonists & inhibitors
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Epidermal Growth Factor / pharmacology
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ErbB Receptors / antagonists & inhibitors
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Humans
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Molecular Structure
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Phosphorylation
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Pyrimidines / chemical synthesis*
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Pyrimidines / pharmacology*
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Receptor, Adenosine A1 / metabolism
Substances
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Adenosine A1 Receptor Antagonists
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Pyrimidines
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Receptor, Adenosine A1
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Epidermal Growth Factor
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ErbB Receptors