After correlation of the majority of signals by COSY and one-bond heteronuclear correlation, the complete assignment of the 'H and I3C NMR spectra of the macrolide antibiotic venturicidin A required the application of long-range CH coupling information. This was accessible by the COLOC-S and selecti
The complete 1H NMR assignments of aminoglycoside antibiotics and conformational studies of butirosin A through the use of 2D NMR spectroscopy
โ Scribed by James R. Cox; Engin H. Serpersu
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 409 KB
- Volume
- 271
- Category
- Article
- ISSN
- 0008-6215
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โฆ Synopsis
The complete proton assignments of the aminoglycoside antibiotics, butirosin A, kanamycin A and kanamycin B, at pH 6.5 have been made through the use of various homonuclear and heteronuclear 2D NMR methods. Butirosin A NOESY experiments suggest a stacking arrangement between the xylose and 2,6-diamino-2,6-dideoxyglucose rings, while the 2-deoxystreptamine ring and its substituent, the (S)-4-amino-2-hydroxybutyryl group, extend away from the stacked rings. Informative long-range NOEs were observed for butirosin A but not with kanamycin A or kanamycin B. Many intra-ring NOEs were observed with all three aminoglycosides that confirm the proton assignments made in this study.
๐ SIMILAR VOLUMES
The complete assignments of 1H and 13C data for Sch 27899 are described. The compound is an oligosaccharide antibiotic belonging to the class everninomicin. It has a molecular mass of 1629. The assignments are based on 2D HMQC, HMQC-TOCSY and HMBC experiments.
Colominic acid (1) is homologous to the weakly immunogenic group B capsular polysaccharide produced by Neisserria meningitidis that causes meningitis in humans [1].
## Abstract ^1^H and ^13^C NMR spectra of the 32โmembered pentaene macrolide flavofunginโI (identical with mycoticin A) in DMSOโ__d__~6~ solution were fully assigned employing a combination of various 1D and 2D homoโ and heteroโnuclear experiments. Secondary deuterium isotope shifts measured in the