TY - JOUR
T1 - Effects of chalcone derivatives on lipoxygenase and cyclooxygenase activities of mouse epidermis
AU - Nakadate, Teruo
AU - Aizu, Eriko
AU - Yamamoto, Satoshi
AU - Kato, Ryuichi
N1 - Funding Information:
Part of this work was supported by Grants-in Aid for Cancer Research and for Encouragement of Young Scientists, from the Ministry of Education, Science Culture of Japan.
PY - 1985/9
Y1 - 1985/9
N2 - The effects of chalcone derivatives on 12-lipoxygenase and cyclooxygenase of mouse epidermis were investigated. The chalcone derivatives which have 3,4-dihydroxycinnamoyl structure in the molecule, such as 3,4-dihydroxychalcone, 3,4,2′-trihydroxychalcone, 3,4,4′-trihydroxychalcone and 3,4,2′4′-tetrahydroxychalcone, potently inhibited epidermal 12-lipoxygenase activity. Although some of them also inhibited cyclooxygenase activity at relatively high concentrations, the inhibitory effects of these chalcone derivatives on 12-lipoxygenase were 10 times or more potent than their effects on cyclooxygenase. The chalcone derivatives which have cinnamoyl or 4-hydroxycinnamoyl structure, instead of 3,4-dihydroxycinnamoyl structure, in the molecule, showed little or no inhibitory effects on either 12-lipoxygenase or cyclooxygenase activities. The inhibitory effects of chalcone derivatives on 12-lipoxygenase and cyclooxygenase of mouse epidermis are dependent on the particular structure, i.e. 3,4-dihydroxycinnamoyl structure, of the chalcone derivatives.
AB - The effects of chalcone derivatives on 12-lipoxygenase and cyclooxygenase of mouse epidermis were investigated. The chalcone derivatives which have 3,4-dihydroxycinnamoyl structure in the molecule, such as 3,4-dihydroxychalcone, 3,4,2′-trihydroxychalcone, 3,4,4′-trihydroxychalcone and 3,4,2′4′-tetrahydroxychalcone, potently inhibited epidermal 12-lipoxygenase activity. Although some of them also inhibited cyclooxygenase activity at relatively high concentrations, the inhibitory effects of these chalcone derivatives on 12-lipoxygenase were 10 times or more potent than their effects on cyclooxygenase. The chalcone derivatives which have cinnamoyl or 4-hydroxycinnamoyl structure, instead of 3,4-dihydroxycinnamoyl structure, in the molecule, showed little or no inhibitory effects on either 12-lipoxygenase or cyclooxygenase activities. The inhibitory effects of chalcone derivatives on 12-lipoxygenase and cyclooxygenase of mouse epidermis are dependent on the particular structure, i.e. 3,4-dihydroxycinnamoyl structure, of the chalcone derivatives.
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U2 - 10.1016/0090-6980(85)90112-1
DO - 10.1016/0090-6980(85)90112-1
M3 - Article
C2 - 3933054
AN - SCOPUS:0022381067
SN - 0090-6980
VL - 30
SP - 357
EP - 368
JO - Prostaglandins
JF - Prostaglandins
IS - 3
ER -