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1  tethered by a tetraene diester linker to an aminocoumarin.
2 to NovH or on the subsequently released free aminocoumarin.
3 L-tyrosyl-L-valyl-L-aspartic acid 4-methyl-7-aminocoumarin.
4 -doped pai-extended coumarins derived from 4-aminocoumarin.
5 s derived from beta-lactams, macrolides, and aminocoumarins.
6                                 Libraries of aminocoumarin analogues have been generated by in vivo f
7 nolignol analogs gamma-linked to fluorogenic aminocoumarin and nitrobenzofuran dyes were synthesized
8 ding pockets that separately accommodate the aminocoumarin and polyketide moieties of the antibiotic.
9 thetases which construct amide bonds between aminocoumarins and various acyl moieties.
10 olides, 2 ionophores, 2 diaminopyimidines, 1 aminocoumarin, and 1 lincosamide).
11 yrase inhibitors such as fluoroquinolone and aminocoumarin antibacterials.
12  penultimate step in the biosynthesis of the aminocoumarin antibiotic novobiocin.
13  the specific timing of C-methylation in the aminocoumarin antibiotic pathways is established.
14                                          The aminocoumarin antibiotics clorobiocin and coumermycin A(
15 he 5-methyl-2-pyrrolylcarbonyl moiety of the aminocoumarin antibiotics clorobiocin and coumermycin A1
16                          The biosynthesis of aminocoumarin antibiotics involves the action of amide s
17 During the biosynthesis of the streptomycete aminocoumarin antibiotics novobiocin and the dimeric cou
18                                          The aminocoumarin antibiotics novobiocin, clorobiocin, and c
19 that the plant is sensitive to quinolone and aminocoumarin antibiotics, compounds that target DNA gyr
20 e is indeed the target for the quinolone and aminocoumarin antibiotics.
21 dem to create additional variants of dimeric aminocoumarin antibiotics.
22                                          The aminocoumarin class of antibiotics, exemplified by novob
23               The caging group 7-N,N-diethyl aminocoumarin (DECM) was used to cage the gamma-carboxyl
24 rin 461 (C461), both belong to a family of 7-aminocoumarin dyes that have distinctive fluorescence li
25          Coumermycin A(1) is a member of the aminocoumarin family of antibiotics.
26 cin A(1), the phenolic hydroxyl group of the aminocoumarin in simocyclinone is not glycosylated with
27 residues in the MHC peptide binding site and aminocoumarin-labeled peptides, we measured real-time ki
28 tes were identified upon screening an N-acyl aminocoumarin library.
29 terminal subunit of yeast TBP (yTBPc) and an aminocoumarin moiety appended either upstream or downstr
30 ers in the functional dimeric unit, with the aminocoumarin moiety of SD8 buried in the protein core,
31            The bicyclic coumarin ring in the aminocoumarin natural product antibiotics that target ba
32 e formation of E. coli persisters against an aminocoumarin, novobiocin, which targets the GyrB subuni
33 say monitors the decrease in fluorescence of aminocoumarins on acylation.
34 -glutamic-L-valyl-L-aspartic acid 4-methyl-7-aminocoumarin or acetyl-L-tyrosyl-L-valyl-L-aspartic aci
35     Similar experiments on Indo-1, NADH, and aminocoumarin produced similar results and suggest that
36  Escherichia coli and shown to act after the aminocoumarin ring has been constructed by prior action
37 oups installed on the noviosyl moiety of the aminocoumarin scaffold.
38 at predominates in the subsequently cyclized aminocoumarin scaffold.
39 solid-phase synthesis of a library of N-acyl aminocoumarin substrates and the screening procedure to
40 ence-based assay; (ii) the identified N-acyl aminocoumarin substrates are optimized by rapid analog s
41 cence-based assay, (2) the identified N-acyl aminocoumarin substrates are optimized by rapid analogue
42                  Coumermycin A1 is a natural aminocoumarin that inhibits bacterial DNA gyrase, a memb
43                             NovL ligates the aminocoumarin to prenylhydroxybenzoate to yield novobioc
44 akes the bis-amide by tandem ligation of two aminocoumarins to a dicarboxypyrrole.
45 e CouL for mono- and bisamide formation with aminocoumarins to provide substrates for the glycosyltra
46 L-tyrosyl-L-valyl-L-aspartic acid 4-methyl-7-aminocoumarin was resistant to cleavage activity.
47 assisted hybridization strategy, a number of aminocoumarins were designed, prepared, and tested as mo
48 into inhibitors by direct replacement of the aminocoumarin with known mechanism-based pharmacophores.
49 d to inhibitors by direct replacement of the aminocoumarin with known mechanism-based pharmacophores.
50 ists of three steps: (1) a library of N-acyl aminocoumarins with diverse, low molecular weight N-acyl
51 ists of three steps: (i) a library of N-acyl aminocoumarins with diverse, low-molecular-weight N-acyl
52 -glutamic-L-valyl-L-aspartic acid 4-methyl-7-aminocoumarin within 6 hr following etoposide addition,