Two New Analogues of the Cytotoxic Substance BE-52211 from Streptomyces sp.
- 13 December 2003
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Natural Products
- Vol. 67 (1) , 85-87
- https://doi.org/10.1021/np030324b
Abstract
Two new β-hydroxy acetamides, BE-52211 B and BE-52211 C, which were structural analogues of BE-52211, were obtained as an inseparable mixture from an actinomycete, Streptomyces sp. Their structures were elucidated on the basis of spectroscopic data. They inhibited cell division of starfish embryos at a concentration of 2.5 μg/mL or greater.Keywords
This publication has 8 references indexed in Scilit:
- A New α,β,γ,δ-Unsaturated carboxylic acid and three new cyclic peroxides from the marine sponge, Monotria japonica, which selectively lyse starfish oocytes without affecting nuclear morphologyBioorganic & Medicinal Chemistry, 2003
- Novel norsesterterpenes, which inhibit gastrulation of the starfish embryo, from the marine sponge Rhopaloeides sp.Tetrahedron, 1998
- Ancorinoside A: A Novel Tetramic Acid Glycoside from the Marine Sponge, Ancorina sp. Which Specifically Inhibits Blastulation of Starfish EmbryosThe Journal of Organic Chemistry, 1997
- Selective inhibition of exoplasmic membrane fusion in echinoderm gametes with jaspisin, a novel antihatching substance isolated from a marine sponge.Journal of Biological Chemistry, 1994
- Isojaspisin: A novel styryl sulfate from a marine sponge, Jaspis sp., that inhibits hatching of sea urchin embryosTetrahedron Letters, 1994
- Jaspisin, a Novel Styryl Sulfate from the Marine Sponge,JaspisSpeciesBioscience, Biotechnology, and Biochemistry, 1994
- High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoidsJournal of the American Chemical Society, 1991
- Isolation and Identification of Meiosis Inducing Substance in Starfish Asterias amurensisNature, 1969