TY - JOUR
T1 - The inhibitory components from Artocarpus incisus on melanin biosynthesis
AU - Shimizu, Kuniyoshi
AU - Kondo, Ryuichiro
AU - Sakai, Kokki
AU - Lee, Seon Ho
AU - Sato, Hiroaki
PY - 1998/7/13
Y1 - 1998/7/13
N2 - The inhibitory effects of methanol extracts of heartwood of 23 Papua New Guinean wood species on tyrosinase activity were examined. The extract of Artocarpus incisus showed the strongest tyrosinase inhibitory activity which was equivalent to kojic acid. The extract apparently inhibited melanin biosynthesis of both cultured B16 melanoma cells without any cytotoxicity and in the back of a brown guinea pig without skin irritation. Thus, the potentiality of the extracts of heartwood of R. incisus both as material of a useful skin whitening agent and as a remedy for disturbances in pigmentation is evident. Tyrosinase inhibitory activity-guided fractionation led to the isolation of seven active compounds including a new compound which has been characterized as 6-(3'-methyl-1'-butenyl)-5,7,2',4'-tetrahydroxyflavone, named isoartocarpesin. Other active compounds were (+)-dihydromorin, chlorophorin, (+)-norartocarpanone, 4-prenyloxyresveratrol, artocarbene, and artocarpesin. These compounds are probably responsible for the melanin biosynthesis inhibitory effects.
AB - The inhibitory effects of methanol extracts of heartwood of 23 Papua New Guinean wood species on tyrosinase activity were examined. The extract of Artocarpus incisus showed the strongest tyrosinase inhibitory activity which was equivalent to kojic acid. The extract apparently inhibited melanin biosynthesis of both cultured B16 melanoma cells without any cytotoxicity and in the back of a brown guinea pig without skin irritation. Thus, the potentiality of the extracts of heartwood of R. incisus both as material of a useful skin whitening agent and as a remedy for disturbances in pigmentation is evident. Tyrosinase inhibitory activity-guided fractionation led to the isolation of seven active compounds including a new compound which has been characterized as 6-(3'-methyl-1'-butenyl)-5,7,2',4'-tetrahydroxyflavone, named isoartocarpesin. Other active compounds were (+)-dihydromorin, chlorophorin, (+)-norartocarpanone, 4-prenyloxyresveratrol, artocarbene, and artocarpesin. These compounds are probably responsible for the melanin biosynthesis inhibitory effects.
UR - http://www.scopus.com/inward/record.url?scp=0031806944&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0031806944&partnerID=8YFLogxK
U2 - 10.1055/s-2006-957470
DO - 10.1055/s-2006-957470
M3 - Article
C2 - 9690341
AN - SCOPUS:0031806944
VL - 64
SP - 408
EP - 412
JO - Planta Medica
JF - Planta Medica
SN - 0032-0943
IS - 5
ER -