Concepedia

Notoamides F−K, Prenylated Indole Alkaloids Isolated from a Marine-Derived <i>Aspergillus</i> sp.

Sachiko Tsukamoto, Hikaru Kato, Masayuki Samizo, Yuka Nojiri, Hiroyuki Onuki, Hiroshi Hirota, Tomihisa Ohta

Journal of Natural Products · 2008 · 133 citations · 22 references

DOI

Concepts

Abstract

Six new prenylated indole alkaloids, named notoamides F-K (8-13), were isolated from a marine-derived Aspergillus sp. Their structures, including absolute configurations, were elucidated by spectroscopic methods. Notoamide I (11) showed weak cytotoxicity against HeLa cells with an IC(50) value of 21 microg/mL.

References

22

Notoamides A–D: Prenylated Indole Alkaloids Isolated from a Marine‐Derived Fungus, <i>Aspergillus</i> sp.

Hikaru Kato, Takushi Yoshida, Takanori Tokue et al. · Angewandte Chemie International Edition · 2007 · 271 citations · Full text

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Stephacidin A and B:  Two Structurally Novel, Selective Inhibitors of the Testosterone-Dependent Prostate LNCaP Cells

Jingfang Qian‐Cutrone, Stella Huang, Yue‐Zhong Shu et al. · Journal of the American Chemical Society · 2002 · 222 citations

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The structure of paraherquamide, a toxic metabolite from

Mikio Yamazaki, Emi Okuyama, Makoto Kobayashi et al. · Tetrahedron Letters · 1981 · 202 citations

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Studies in relation to biosynthesis—XLIV

Arthur J. Birch, Richard A. Russell · Tetrahedron · 1972 · 152 citations

, , +4