2005
DOI: 10.1016/j.bcp.2005.04.016
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Inhibition of the mitochondrial ATP synthesis by polygodial, a naturally occurring dialdehyde unsaturated sesquiterpene

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Cited by 39 publications
(35 citation statements)
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“…Dill oil inhibited an isolated mitochondrial ATPase in a dose-dependent manner at different concentrations, which manifests the idea of mitochondrial ATPase being a physiologically relevant target of dill oil in A. flavus . Similar types of results were also reported by Lunde et al [44] and Castelli et al [42].…”
Section: Discussionsupporting
confidence: 90%
“…Dill oil inhibited an isolated mitochondrial ATPase in a dose-dependent manner at different concentrations, which manifests the idea of mitochondrial ATPase being a physiologically relevant target of dill oil in A. flavus . Similar types of results were also reported by Lunde et al [44] and Castelli et al [42].…”
Section: Discussionsupporting
confidence: 90%
“…The surface potential (Gouy-Chapman, s ) contributestogether with the membrane dipole potential ( d ) and the transmembrane potentials ( ) -to the potential difference between the membrane surfaces ( ϕ) and determines the electrical potential profile in the membrane [48]. Therefore, the change of the surface potential by MDpep5 would affect the potential profile in the membrane and the interfacial membrane potential difference ( ϕ).…”
Section: Effect Of Mdpep5 On the Bacterial Electrostatic Surface Potementioning
confidence: 98%
“…Polygodial was identified by comparison of its retention time (17.62 min) and the MS spectrum with an authentic sample obtained from our previous works (Castelli et al, 2005;Malheiros et al, 2005;Derita et al, 2008). The linearity of the detector response was verified using a series of two-fold diluted DCM solutions of polygodial.…”
Section: Quantification Of Polygodial In Extracts From L S and F Colmentioning
confidence: 99%
“…Repeated column chromatographies of fractions 5-8 led to the isolation of the sesquiterpenes polygodial (1) (1925 mg), isopolygodial (2) (70 mg), drimenol (3) (30 mg) and confertifolin (4) (35 mg). Pure compounds were identified by micromelting point, optical rotation and spectroscopic data including 1 H and 13 CNMR (Ying et al, 1995;Barnes and Loder, 1962;Guillerm et al, 1984) and were compared with authentic samples obtained previously in our laboratory (Castelli et al, 2005;Malheiros et al, 2005;Derita et al, 2008 for polygodial and isopolygodial) or with literature data (Rodríguez et al, 2005;Urban and Capon, 1996, for drimenol;Hueso-Rodríguez and Rodríguez, 1989;Appel et al, 1963, for confertifolin).…”
Section: Bioassay-guided Fractionation Of Adcmmentioning
confidence: 99%