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

European Journal of Medicinal Chemistry

Volumn 45, Issue 12, 2010, Pages 5567-5575

  Lee, Kyeong ^a   Lee, Jee Hyun ^b   Boovanahalli, Shanthaveerappa K ^a   Choi, Yongseok ^c   Choo, Soo Jin ^d   Yoo, Ick Dong ^d   Kim, Dong Hee ^e   Yun, Mi Young ^f   Lee, Gye Won ^g   Song, Gyu Yong ^b  

^a Dongguk University   (South Korea)

^b Chungnam National University   (South Korea)

^c Korea University   (South Korea)

^d Korea Research Institute of Bioscience and Biotechnology (KRIBB)   (South Korea)

^e Daejeon University   (South Korea)

^f Byuksung College   (South Korea)

^g Konyang University   (South Korea)

Author keywords

(+) Decursin; (+) Decursinol; (+) Decursinol angelate; Melanin inhibitors

Indexed keywords

2 METHOXY PHENYLPROPIONIC ACID ACID 8,8 DIMETHYL 2 OXO 6,7 DIHYDRO 2H,8H PYRANO[3,2 G]CHROMEN 7 YL ESTER; 3 (2 METHOXY PHENYL)ACRYLIC ACID ACID 8,8 DIMETHYL 2 OXO 6,7 DIHYDRO 2H,8H PYRANO[3,2 G]CHROMEN 7 YL ESTER; 3 (2 THIENYL)ACRYLIC ACID ACID 8,8 DIMETHYL 2 OXO 6,7 DIHYDRO 2H,8H PYRANO[3,2 G]CHROMEN 7 YL ESTER; 3 PHENYL ACRYLIC ACID ACID 8,8 DIMETHYL 2 OXO 6,7 DIHYDRO 2H,8H PYRANO[3,2 G]CHROMEN 7 YL ESTER; ALPHA INTERMEDIN; ANTINEOPLASTIC AGENT; DECURSIN; DECURSINOL; DECURSINOL ANGELATE; MELANIN; PHENYLPROPIONIC ACID 8,8 DIMETHYL 2 OXO 6,7 DIHYDRO 2H,8H PYRANO[3,2 G]CHROMEN 7 YL ESTER; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CYTOTOXICITY; DRUG SYNTHESIS; MELANOMA CELL; NONHUMAN;

ANIMALS; BENZOPYRANS; BUTYRIC ACIDS; CELL LINE, TUMOR; CELL PROLIFERATION; MELANINS; MELANOMA, EXPERIMENTAL; MICE; MOLECULAR STRUCTURE; STEREOISOMERISM; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 78649269475     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2010.09.006     Document Type: Article

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