Antineoplastic agents.: 380.: Isolation and X-ray crystal structure determination of isoaaptamine from the Republic of Singapore Hymeniacidon sp and conversion to the phosphate prodrug hystatin 1

被引:37
作者
Pettit, GR [1 ]
Hoffmann, H
McNulty, J
Higgs, KC
Murphy, A
Molloy, DJ
Herald, DL
Williams, MD
Pettit, RK
Doubek, DL
Hooper, JNA
Albright, L
Schmidt, JM
Chapuis, JC
Tackettt, LP
机构
[1] Arizona State Univ, Canc Res Inst, Tempe, AZ 85287 USA
[2] Arizona State Univ, Dept Chem & Biochem, Tempe, AZ 85287 USA
[3] Queensland Museum, Sessile Marine Invertebrates, Brisbane, Qld 4101, Australia
[4] Western Oregon State Univ, Dept Biol, Monmouth, OR 97361 USA
来源
JOURNAL OF NATURAL PRODUCTS | 2004年 / 67卷 / 03期
关键词
D O I
10.1021/np0204592
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
By use of bioassay (murine P388 lymphocytic leukemia cell line) guided isolation procedures, extracts of the Republic of Singapore marine sponge Hymeniacidon sp. were found to contain demethyl-oxyaaptamine (1) and aaptamine (3) as prominent cancer cell growth inhibitory constituents accompanied by the trace, albeit more active, component isoaaptamine (4). The isolation, X-ray structure elucidation, and antineoplastic and antimicrobial activities of isoaaptamine (4) have been summarized. Because of instability, isoaaptamine (4) was converted to a stable sodium phosphate prodrug designated hystatin 1 (7).
引用
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页码:506 / 509
页数:4
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