CHEMISTRY OF RENIERAMYCINS. 16. STRUCTURE OF 7-DEMETHYLRENIERAMYCIN O (=14α-HYDROXYRENIERAMYCIN S) FROM BLUE SPONGE, XESTOSPONGIA sp.

被引:8
作者
Saito, Naoki [1 ]
Hiramatsu, Ai [1 ]
Hirade, Hiromi [1 ]
Kubota, Mitsue [1 ]
Toyoshima, Ryoko [1 ]
Fujino, Akiya [1 ]
Sirimangkalakitti, Natchanun [2 ]
Suwanborirux, Khanit [2 ]
Concepcion, Gisela P. [3 ]
机构
[1] Meiji Pharmaceut Univ, Grad Sch Pharmaceut Sci, 2-522-1 Noshio, Tokyo 2048588, Japan
[2] Chulalongkorn Univ, Fac Pharmaceut Sci, Dept Pharmacognosy & Pharmaceut Bot, Ctr Bioact Nat Prod Marine Organisms & Endophyt F, Bangkok 10330, Thailand
[3] Univ Philippines, Marine Sci Inst, Quezon City 1101, Philippines
关键词
Isoquinoline; Anticancer Activity; Structure Determination; Renieramycin; Structure Transformation; NUDIBRANCH JORUNNA-FUNEBRIS; ISOQUINOLINEQUINONE ALKALOIDS; POTASSIUM CYANIDE; ECTEINASCIDIN; 770; DERIVATIVES; CYTOTOXICITY;
D O I
10.3987/COM-16-S(S)77
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A new renieramycin-type marine natural product was isolated from the blue sponge Xestospongia sp. found in the Philippines and Thailand, and its structure was elucidated to be 7-demethylrenieramycin 0 (= 14 alpha-hydroxyrenieramycin S, 1) by comparing its spectral data with those of renieramycins 0 and S. Exposure of a dichloromethane solution of renieramycin 0 to sunlight gave compound 1 along with renieramycin U. Compound 1 showed weak cytotoxicity to several human cancer cell lines.
引用
收藏
页码:748 / 752
页数:5
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