Arachidonic acid amide inhibitors of gap junction cell-cell communication

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Parallel synthesis and evaluation of 132 (+)-1,2,9,9a-tetrahydrocyclopropa[c]benz[e]indol-4-one (CBI) analogues of CC-1065 and the duocarmycins defining the contribution of the DNA-binding domain.

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Caffeic acid phenethyl ester derivatives inhibit glyoxalase I activity and induce cell death in cultured cancer cell lines.

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Arachidonic acid amide inhibitors of gap junction cell-cell communication

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Arachidonic acid amide inhibitors of gap junction cell-cell communication

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