Kanamycin Kanamycin

Kanamycin Kanamycin, 0-3-amino-3-deoxy-a-D-glncopyranosyl-(l—>6)-0-[6-deoxy-6-amino-a-D-glucopyranosyl-(l—>4)]-2-deoxy-D-streptamine (3.4.6), is isolated from a cultnre liquid of the actinomycete S. kanamyceticus, which produces three antibiotics— kanamycines A, B, and C [259-262]. [Pg.479]

Kanamycin Kanamycin A AU except Fi MlOO, FlOO, L600, K2500, —... [Pg.87]

Kanamycines kanamycines Karaya Gum karaya Kenaf kenaf... [Pg.347]

Kakaobutter beurre de cacao Kampfer camphre Kanamycine kanamycines Karaya Gummi karaya Karnaubapalme palmier carnauba Karnaubawachs cire de carnauba Karoffelprotein proteine de pommes de terre... [Pg.359]

Kakao Cocoa Kakaobutter Cocoa Butter Kampfer Camphor Kanamycine Kanamycines Karaya Gummi Karaya Gum Karnaubapalme Carnauba Karnaubawachs Carnauba Wax Karoffelprotein Potato Protein Kartoffel Potato Kartoffelpiilpe Potato Pulp Feed Kartoffelstarkegewinnung Potato Starch Production... [Pg.371]

Among the older aminoglycoside derivatives, kanamycin A and sisomicin were, at one time, a significant part of medical practice, but have now been largely replaced by the compounds Hsted in Table 1. Streptomycin is stiH used in a few restricted situations. [Pg.480]

N-ethyl kanamycin A (153) has some resistance to APH(3 ), ANT(2 ), and AAC(3). Butakacin [59733-86-7] C22H N 0 2 t i l-A/-(3)-2-hydroxy-4-aminobutyl derivative of kanamycin A (154), has antimicrobial properties similar to amikacin. A similar effect was seen with the l-A/-(l,3-dihydroxy-2-propyl) derivative of kanamycin B, propikacin [66887-96-5] C22H42N 022 (155). Methylation of the 6 -amine reduces susceptibility to AAC(6 ) (156). [Pg.484]

The 1-epi analogue of tobramycia (4) was slightly less active than the parent, but the 3-epi was almost iaactive (166). Epimerization at the 1-position had a more detrimental effect with kanamycin A (166,167). [Pg.484]

R" = H), were isolated from Streptomjces hofunensis (181,182). Of these, factor 5 has the best antibacterial activity, and is comparable ia poteacy to kanamycin A (5, R = H). 3 -Deoxyseldomycia factor 5 (183) was fouad to be more active than the parent compound, while the 3 -epi analogue was less active (184). [Pg.484]

Kamlet-Taft solvent parameters, 2, 123 Kanamycins episulfides... [Pg.693]

L-(-)-7-Ami no-a-hydroxybutyric Acid N-hydroxysuccinim ide 6 -Monobenzyloxy[Pg.58]

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