Synthesis of (S)-(+)-decursin and its analogues as potent inhibitors of melanin formation in B16 murine melanoma cells

We report the synthesis of a novel series of highly potent melanin inhibitors which were obtained through structural modification of an anticancer compound S-(+)-decursinol. The in vitro inhibitory potencies of the newly synthesized compounds were evaluated against α-MSH induced melanin production i...

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Veröffentlicht in:European journal of medicinal chemistry 2010-12, Vol.45 (12), p.5567-5575
Hauptverfasser: Lee, Kyeong, Lee, Jee-Hyun, Boovanahalli, Shanthaveerappa K., Choi, Yongseok, Choo, Soo-Jin, Yoo, Ick-dong, Kim, Dong Hee, Yun, Mi Young, Lee, Gye Won, Song, Gyu-Yong
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Sprache:eng
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