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1 tential role of each residue of this complex glycopeptide antibiotic.
2 is highly reproducible and selective toward glycopeptide antibiotics.
3 larization based method for the detection of glycopeptide antibiotics.
4 activities, and probably the structures, of glycopeptide antibiotics.
5 to desolvation of the ligand binding site in glycopeptide antibiotics.
6 the vancomycin and the teicoplanin class of glycopeptide antibiotics.
7 omycin, a member of the vancomycin family of glycopeptide antibiotics.
8 rinsic resistance to the vancomycin class of glycopeptide antibiotics.
9 showed a mechanistic distinction from other glycopeptide antibiotics.
10 s and keratinimicins are recently discovered glycopeptide antibiotics.
11 that by blocking autolysin function, type V glycopeptide antibiotics are promising antivirulence age
14 ichia coli, which is never challenged by the glycopeptide antibiotics because they cannot penetrate t
16 -Ala cell wall precursor to d-Ala-d-Lac upon glycopeptide antibiotic challenge, displaying a potency
18 ible for biosynthesis of the vancomycin-type glycopeptide antibiotic chloroeremomycin was recently se
19 ted a streamlined total synthesis of the new glycopeptide antibiotic class by removing the challenges
20 class of glycopeptide antibiotics-the known glycopeptide antibiotic complestatin and a newly discove
22 es seen in three other crystal structures of glycopeptide antibiotics complexed with peptide ligands.
28 he discovery of vancomycin in the 1950s, the glycopeptide antibiotics (GPAs) have been of great inter
37 lently immobilising teicoplanin and/or other glycopeptide antibiotics in the pursuit of novel antibac
38 ence of resistance to vancomycin and related glycopeptide antibiotics is spurring efforts to develop
39 e bleomycins (BLMs) are structurally related glycopeptide antibiotics isolated from Streptomyces vert
40 oxide was functionalized with vancomycin, a glycopeptide antibiotic known to have a specific interac
42 to protoplasts that were pretreated with the glycopeptide antibiotic phleomycin, a nonspecific DNA do
46 ramoplanin is structurally less complex than glycopeptide antibiotics such as vancomycin, peptidomime
49 ial interactions of the last line of defence glycopeptide antibiotic teicoplanin with an ocular mucin
50 quantitate the binding affinity between the glycopeptide antibiotics teicoplanin from Actinoplanes t
51 results suggest new strategies for designing glycopeptide antibiotics that overcome bacterial resista
52 nt of a class of highly potent semisynthetic glycopeptide antibiotics, the guanidino lipoglycopeptide
53 e essential to understanding the activity of glycopeptide antibiotics, the recognition of pathogens b
54 red two members of a new functional class of glycopeptide antibiotics-the known glycopeptide antibiot
55 ed total syntheses of vancomycin and related glycopeptide antibiotics, their agylcons, and key analog
56 internuclear distances from the 19F of this glycopeptide antibiotic to natural-abundance 31P and to
57 ws that the same H-bonding framework used by glycopeptide antibiotics to bind peptidoglycan termini i
58 nked the Lys-D-Ala-D-Ala binding epitope for glycopeptide antibiotics to three different carrier prot
64 ly established dimerization of the important glycopeptide antibiotic vancomycin in four different aqu
66 t the Amycolatopsis sp. BCA-696 produces the glycopeptide antibiotic vancomycin that inhibits the gro
74 al component of the mannopeptimycins, cyclic glycopeptide antibiotics with activity against drug-resi
76 ycin, and we show that the activity of other glycopeptide antibiotics with this feature can also be s