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- W2014976143 abstract "The cyclic tetrapeptide tentoxin and the conformationally related analog [Pro 1 ] tentoxin have been synthesized by a new solution methodology. D, L‐3‐phenyl‐serine was employed as a synthetic precursor to the Z‐dehydrophenylalanine substituent. Increased yields of both compounds were obtained when a modified cyclization procedure was employed through ring closure from the N‐terminal substituents of N‐methylalanine and proline to a C‐terminal glycine. Biological activities were determined in a seedling assay used to measure chlorosis induction. Both tentoxin and [Pro 1 ] tentoxin exhibited similar chlorosis inducing activity. Whole leaf extracts of chlorotic, [Pro 1 ] tentoxin‐treated seedling leaves lacked active polyphenoloxidase when subjected to electrophoretic analysis. Coupling factor 1 (CF 1 ) ATPase isozymes were assayed for ATPase activity in 10μuM‐100 μuM solutions of tentoxin and [Pro 1 ] tentoxin. CF 1 ATPase inhibition was observed for both tentoxin and [Pro 1 ] tentoxin. Inhibition of a single ATPase isozyme by tentoxin was alleviated at or above 50μuM while [Pro 1 ] tentoxin inhibited two CF 1 ATPases at concentrations up to 110μuM. No alleviation of ATPase inhibition was noted for higher concentrations of [Pro 1 ] tentoxin." @default.
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- W2014976143 date "1986-12-01" @default.
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- W2014976143 title "New synthesis and biological activity of the cyclic tetrapeptides tentoxin and [Pro 1] tentoxin" @default.
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- W2014976143 doi "https://doi.org/10.1111/j.1399-3011.1986.tb03298.x" @default.
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