1957
DOI: 10.1002/lipi.19570590503
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Potentiometrische Oxydationsstudien über die funktionelle Inhibitor‐Wirkung des Gossypols

Abstract: Fur die autoxydationshemmende Wirkung des Gossypols sind die 4 OH‐Gruppen in 6,6′‐ und 7,7′‐Stellung verantwortlich, während die 1,1′‐ständigen OH‐Gruppen keine inhibierende Wirkung besitzen. Die in 8,8′‐Stellung befindlichen Aldehyd‐Gruppen üben einen die antioxygene Aktivität steigernden Einfluß aus, was durch ihre Oxydation sowie durch das Vorliegen tautomerer Formen erklärt werden kann.

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Cited by 6 publications
(1 citation statement)
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“…Certain aromatic amines, for example N:N-diisopropyl-p-phenylene diamine and its nitro-derivatives exhibit an anti-oxidative action although these products do not possess an active hydroxylgroup. Here the mechanism still cannot be satisfactorily explained (Kaufmann & Korthage, 1953;Bakes, 1954;Wachs, 1957). Another group of anti-oxidants are the reductants, which offer a more reactive substrate to oxygen than do the lipids themselves.…”
Section: Rh-^rmentioning
confidence: 99%
“…Certain aromatic amines, for example N:N-diisopropyl-p-phenylene diamine and its nitro-derivatives exhibit an anti-oxidative action although these products do not possess an active hydroxylgroup. Here the mechanism still cannot be satisfactorily explained (Kaufmann & Korthage, 1953;Bakes, 1954;Wachs, 1957). Another group of anti-oxidants are the reductants, which offer a more reactive substrate to oxygen than do the lipids themselves.…”
Section: Rh-^rmentioning
confidence: 99%