Some attempts to obtain a more simple crystalline derivative containing o heavy atom and suitable for the analysis were unsuccessful. Reduction with lithium aluminum deuteride afforded bisdeoxo N-methylcycloshowdomycin acetonide-d4. The details was read by one of us, Tsukudo at the 20th Annual Meeti
The structure of a new nucleoside antibiotic, capuramycin
β Scribed by Haruo Seto; Noboru Otake; Shingo Sato; Hiroshi Yamaguchi; Kinji Takada; Masayoshi Itoh; Helen S.M. Lu; Jon Clardy
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- French
- Weight
- 260 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
The structure of capuramycin has been determined to be an uracll nucleoside with a caprolactam substltuent as shown in Fig. 5 by NMR spectral analysis, chemical degradation and X-ray analysis.
During the course of our screening program for new antibiotics, it was found that Streptomyces nrlseus 446-S3 produced a new nucleoslde antibiotic which we have named capuramycln (I).
This antibiotic was isolated from the fermentation broth by adsorption on HP-20 followed by silica gel (CHC13:MeOH =
π SIMILAR VOLUMES
In a recent report ', the structure originally advanced for the nucleoside antibiotic, gougerotin, (I) 3 was revised to structure II on the basis of chemical and physical evidence. The establishment of the carbohydrate moiety as a 4-aminohexose derivative and the positional assignment of the peptid
The structure of a new antibiotic, hygrolidin has been determined as shown in Fig. 3.
The structure of a new antibiotic, roseophilin, was elucidated to be as shown iu Fig. 1 by NMR spectral analysis including a variety of two-dimensional techniques. Roseophilin was found to possess a novel skeleton containing pyrrole and furan moieties.