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Structure–activity relationships of the ultrapotent vanilloid resiniferatoxin (RTX): The homovanillyl moiety

G Appendino, A Ech-Chahad, A Minassi…

文献索引:Appendino, Giovanni; Ech-Chahad, Abdellah; Minassi, Alberto; Bacchiega, Sara; Petrocellis, Luciano De; Marzo, Vincenzo Di Bioorganic and Medicinal Chemistry Letters, 2007 , vol. 17, # 1 p. 132 - 135

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被引用次数: 15

摘要

Starting from ROPA (2), analogues of RTX (1a) modified on the acyl side chain were prepared and evaluated for vanilloid activity in HEK-293 cells over-expressing the human recombinant TRPV1. The ROPA motif provided an enhancement of potency sufficient to expand the range of vanillyl surrogates to structural elements (eg, an unsubstituted phenyl ring) that afford inactive analogues in compounds from the capsaicin series.