The complete relative and absolute configurations of (+)-thiazinotrienomycin E, a potent new ansatrienin cancer cell growth inhibitory agent, have been determined via degradation and chemical correlation.
Furaquinocins A-G: relative and absolute stereochemistry
β Scribed by Peter G. Dormer; Amos B. Smith III; Shinji Funayama; Satoshi Omura
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- French
- Weight
- 292 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
The complete relative and absolute stereochemistry of furaquinocins A-G, a family of cytotoxic antibiotics, have been assigned via a combination of X-ray crystallography, NMR analysis of the derived Mosher esters, and chemical correlation. Komiyama et al. at the Kitasato Institute recently reported the isolation, physicochemical, and biological characteristics of furaquinocins A (1) and B {2). 1 These novel antibiotics, obtained from the fermentation broth of Streptomyces sp. KO-3988, exhibited strong
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