Zobrazeno 1 - 9
of 9
pro vyhledávání: '"D. C. Eustice"'
Autor:
D. C. Eustice, Chia-Lin J. Wang, P. T. Bartholomew, M. Forbes, David R. Brittelli, Andrew M. Slee, M. A. Wuonola, R. J. Mcripley, W. A. Gregory, V. S. Eberly
Publikováno v:
Journal of Medicinal Chemistry. 33:2569-2578
The synthesis and structure-activity relationship (SAR) studies of the effect of varying the "A" group in a series of 5-(acetamidomethyl)oxazolidonone antibacterials (2) are described. Compounds 2 were principally prepared either by the six-step synt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08ae7d5de14ba9bd56c9ab466850c168
https://doi.org/10.1021/jm00171a035
https://doi.org/10.1021/jm00171a035
Publikováno v:
Journal of Biological Chemistry. 265:2733-2739
The yeast Saccharomyces cerevisiae contains two forms of cytochrome c, iso-1-cytochrome c and iso-2-cytochrome c, encoded by the genes CYC1 and CYC7, respectively. The amino acid sequences of these two isozymes are approximately 80% identical. Cyc3-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20231f63a69cc133993b35cba73a1e5b
https://doi.org/10.1016/s0021-9258(19)39863-1
https://doi.org/10.1016/s0021-9258(19)39863-1
Publikováno v:
BioTechniques. 11(6)
A sensitive method has been developed for the detection of E. coli beta-galactosidase in transfected HeLa cells. The chromogenic substrate, CPRG (chlorophenol red-beta-D-galactopyranoside), was compared with ONPG (o-nitrophenyl-beta-D-galactopyranosi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::df98357cf7f8d3bc10b5d6542d3fd186
https://pubmed.ncbi.nlm.nih.gov/1809326
https://pubmed.ncbi.nlm.nih.gov/1809326
Publikováno v:
The Journal of biological chemistry. 265(5)
The yeast Saccharomyces cerevisiae contains two forms of cytochrome c, iso-1-cytochrome c and iso-2-cytochrome c, encoded by the genes CYC1 and CYC7, respectively. The amino acid sequences of these two isozymes are approximately 80% identical. Cyc3-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c611087e205c059e9f0b80fbfa6618aa
https://pubmed.ncbi.nlm.nih.gov/2154458
https://pubmed.ncbi.nlm.nih.gov/2154458
Autor:
W. A. GREGORY, D. R. BRITTELLI, C.-L. J. WANG, M. A. WUONOLA, R. J. MCRIPLEY, D. C. EUSTICE, V. S. EBERLY, P. T. BARTHOLOMEW, A. M. SLEE, M. FORBES
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfa6596164f9e685430e95161c8f7c33
https://doi.org/10.1002/chin.199002183
https://doi.org/10.1002/chin.199002183
Publikováno v:
Drugs under experimental and clinical research. 16(4)
The 3-aryl-2-oxooxazolidinones are a new class of synthetic antibacterial agents that potently inhibit protein synthesis. An automated pulse labelling method with [3H]-lysine was developed with Bacillus subtilis to obtain additional quantitative acti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6576053c25cda4417561335d5827a5f0
https://pubmed.ncbi.nlm.nih.gov/2127566
https://pubmed.ncbi.nlm.nih.gov/2127566
Publikováno v:
Molecular and Cellular Biology. 5:1839-1846
The CYC1-239-O mutation in the yeast Saccharomyces cerevisiae produces a -His-Leu- replacement of the normal -Ala-Gly- sequence at amino acid positions 5 and 6, which lie within a dispensable region of iso-1-cytochrome c; this mutation can accommodat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa35d01a3cb84c5880a889e41eaf8867
https://doi.org/10.1128/mcb.5.8.1839
https://doi.org/10.1128/mcb.5.8.1839
Antibacterials. Synthesis and structure-activity studies of 3-aryl-2-oxooxazolidines. 1. The B group
Autor:
W A, Gregory, D R, Brittelli, C L, Wang, M A, Wuonola, R J, McRipley, D C, Eustice, V S, Eberly, P T, Bartholomew, A M, Slee, M, Forbes
Publikováno v:
Journal of Medicinal Chemistry. 32:1673-1681
The synthesis and structure/activity studies of the effect of varying the "B" group in a series of oxazolidinone antibacterials (I) are described. Two synthetic routes were used: (1) alkylation of aniline with glycidol followed by dialkyl carbonate h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94747216cbd7c1508848e5aad1933c20
https://doi.org/10.1021/jm00128a003
https://doi.org/10.1021/jm00128a003
Pigmentation mutants of Pseudomonas aeruginosa, selected by observed visual differences in coloration from the wild-type strain, were examined for altered patterns of phenazine synthesis. Three classes of mutants that were incapable of pyocyanine pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75c3392eba74135abd8eaae6d50e336e
https://europepmc.org/articles/PMC218113/
https://europepmc.org/articles/PMC218113/
