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001-es BibID:BIBFORM005283
Első szerző:Solov'eva, S. E.
Cím:New Derivatives of Eremomycin Containing 15N or F Atoms for NMR Study / S. E. Solov'eva, S. S. Printsevskaya, E. N. Olsuf'eva, G. Batta, M. N. Preobrazhenskaya
Dátum:2008
Megjegyzések:New semisynthetic derivatives of eremomycin containing N-15 or F atoms were obtained for studying the antibiotic-target interaction in intact cells of Gram-positive bacteria by REDOR NMR method. Interaction of the terminal carboxyl group of amino acid 7 (AA7) of eremomycin with amines in the presence of PyBOP and TBTU reagents resulted in the corresponding [N-15]-amide, p-fluorobenzylamide, p-fluorophenylpiperazide, and 6-N-(p-fluorobenzyl)aminohexylamide. A selective method of [N-15]-amidation of carboxyl group of amino acid 3 (AA3) of carboxyeremomycin was developed, and the amide of eremomycin containing [N-15] in AA3 amide group near the antibiotic binding pocket was obtained. Carboxyeremomycin bisamides substituted at AA3 and AA7 and containing two atoms of [N-15] or F were obtained from carboxyeremomycin and [N-15]NH4Cl or the corresponding p-fluorobenzylamine hydrochloride in the presence of PyBOP at pH similar to 8. The Edman degradation of eremomycin p-fluorobenzylamide gave de-(D-MeLeu)-eremomycin p-fluorobenzylamide, a hexapeptide derivative incapable of the antibiotic binding with -D-Ala-D-Ala fragment of growing cell wall peptidoglycan. Among the compounds studied, carboxyeremomycin bis-p-fluorobenzylamide showed the best activity against both the glycopeptides-sensitive and glycopeptides-resistant strains of staphylococci and enterococci.
Tárgyszavak:Természettudományok Kémiai tudományok idegen nyelvű folyóiratközlemény külföldi lapban
vancomycin antibiotics
Megjelenés:Russian Journal of Bioorganic Chemistry. - 34 : 6 (2008), p. 747-754. -
További szerzők:Printsevskaya, S. S. Olsuf'eva, E. N. Batta Gyula (1953-) (molekula-szerkezet kutató) Preobrazhenskaya, Maria N.
Internet cím:elektronikus változat
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