Abstract
The synthesis and SAR of a series of 2,4-diamino-quinazoline derivatives as beta-catenin/Tcf-4 inhibitors are described. This series was developed by modifying the initial lead 1, which was identified by screening of our compound library and found to inhibit the beta-catenin/Tcf-4 pathway. Replacement of the biphenyl moiety in compound 1 with the N-phenylpiperidine-4-carboxamide chain as in 2, resulted in a number of new analogues, which are potent inhibitors of the beta-catenin/Tcf-4 pathway. Compound such as 16k exhibited good cellular potency, solubility, metabolic stability and oral bioavailability.
MeSH terms
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Anilides / chemical synthesis
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Anilides / chemistry*
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Anilides / pharmacokinetics
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Animals
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Antineoplastic Agents / chemical synthesis
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Antineoplastic Agents / chemistry*
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Antineoplastic Agents / pharmacokinetics
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Cell Line, Tumor
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Colorectal Neoplasms / drug therapy*
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Female
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Humans
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Mice
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Mice, Nude
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Quinazolines / chemical synthesis
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Quinazolines / chemistry*
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Quinazolines / pharmacokinetics
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Structure-Activity Relationship
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TCF Transcription Factors / antagonists & inhibitors*
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TCF Transcription Factors / metabolism
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Wnt Proteins / antagonists & inhibitors
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Wnt Proteins / metabolism
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Xenograft Model Antitumor Assays
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beta Catenin / antagonists & inhibitors*
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beta Catenin / metabolism
Substances
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Anilides
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Antineoplastic Agents
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Quinazolines
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TCF Transcription Factors
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Wnt Proteins
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beta Catenin