236401-43-7Relevant articles and documents
Synthesis of ring II/III fragment of Kanamycin: A new minimum structural motif for aminoglycoside recognition
Zárate, Sandra G.,Bastida, Agatha,Santana, Andrés G.,Revuelta, Julia
, (2019/08/20)
A novel protocol has been established to prepare the kanamycin ring II/III fragment, which has been validated as a minimum structural motif for the development of new aminoglycosides on the basis of its bactericidal activity even against resistant strains. Furthermore, its ability to act as a AAC-(6′) and APH-(3′) binder, and as a poor substrate for the ravenous ANT-(4′), makes it an excellent candidate for the design of inhibitors of these aminoglycoside modifying enzymes.
Synthesis of kanamycin A analogs containing 6-amino-3-oxa-2,3,4,6-tetradeoxy-D- and -L-glycero-hexopyranose
Kuwahara, Ryuji,Tsuchiya, Tsutomu
, p. 107 - 122 (2007/10/03)
6-Azido-3-oxa-2,3,4,6-tetradeoxy-D- and -L-glycero-hexopyranoses were synthesized in five steps from (2S)- and (2R)-1,2-O-isopropylideneglycerols, respectively. After conversion into the corresponding ethyl 1-thioglycosides, each was condensed with a protected derivative of 6-O-(3-amino-3-deoxy-α-D-glucopyranosyl)-2-deoxystreptamine (16). Deprotection and reduction of the azido group of the condensation products gave the title compounds.
Structure studies on kanamycin.
MAEDA,MURASE,MAWATARI,UMEZAWA
, p. 163 - 165 (2007/10/04)
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