Structure-activity relationships of novel 2-substituted quinazoline antibacterial agents.
about
Aqueous hydrotrope: an efficient and reusable medium for a green one-pot, diversity-oriented synthesis of quinazolinone derivatives.2-(1,3-Benzodioxol-5-yl)-3-phenyl-quinazolin-4(3H)-one.Synthesis and biological evaluation of a novel series of 6,8-dibromo-4(3H)quinazolinone derivatives as anticancer agents.Characterizing the Antimicrobial Activity of N2,N4-Disubstituted Quinazoline-2,4-Diamines toward Multidrug-Resistant Acinetobacter baumannii.In silico molecular docking and in vitro antidiabetic studies of dihydropyrimido[4,5-a]acridin-2-amines.3-(2-Amino-eth-yl)-2-[4-(trifluoro-meth-oxy)anilino]quinazolin-4(3H)-one.2-[2-(2-Anilino-4-oxo-3,4-dihydro-quinazolin-3-yl)phen-oxy]-3-phenyl-quinazolin-4(3H)-one methanol hemisolvate.2-Anilino-3-(2-hy-droxy-phen-yl)quinazolin-4(3H)-one methanol monosolvate.Oxidative dehydrogenation of C-C and C-N bonds: A convenient approach to access diverse (dihydro)heteroaromatic compounds.N-(2,5-Dimeth-oxy-phen-yl)-6-nitro-quinazolin-4-amine.3-(2-Hydroxy-ethyl)-2-(p-tolyl-amino)-quinazolin-4(3H)-one.3,3'-Bis(4-chloro-phen-yl)-2,2'-(m-phenyl-enedi-oxy)diquinazolin-4(3H)-one.3-(2-Amino-ethyl)-2-(4-chloro-anilino)-quinazolin-4(3H)-one methanol 0.75-solvate.Synthesis of quinazolines from N-(2-nitrophenylsulfonyl)iminodiacetate and alpha-(2-nitrophenylsulfonyl)amino ketones via 2H-indazole 1-oxides.Synthesis and in vitro evaluation of N-aryl pyrido-quinazolines derivatives as potent epidermal growth factor receptor inhibitors.Antibacterial aminoglycosides with a modified mode of binding to the ribosomal-RNA decoding site.Synthesis, analytical analysis, and medicinal aspect of novel benzimidazoles and their metal complexes.Hexachlorocyclotriphosphazene (HCCP)-mediated direct formation of thioethers and ethers from quinazolin-4(3H)-ones.Metal-free aerobic oxidative C-N bond cleavage of tertiary amines for the synthesis of N-heterocycles with high atom efficiency.Amiloride as a new RNA-binding scaffold with activity against HIV-1 TAR.Novel benzimidazole analogs as inhibitors of EGFR tyrosine kinase.Facilely accessible quinoline derivatives as potent antibacterial agents
P2860
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P2860
Structure-activity relationships of novel 2-substituted quinazoline antibacterial agents.
description
1999 nî lūn-bûn
@nan
1999 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Structure-activity relationships of novel 2-substituted quinazoline antibacterial agents.
@ast
Structure-activity relationships of novel 2-substituted quinazoline antibacterial agents.
@en
type
label
Structure-activity relationships of novel 2-substituted quinazoline antibacterial agents.
@ast
Structure-activity relationships of novel 2-substituted quinazoline antibacterial agents.
@en
prefLabel
Structure-activity relationships of novel 2-substituted quinazoline antibacterial agents.
@ast
Structure-activity relationships of novel 2-substituted quinazoline antibacterial agents.
@en
P2093
P356
P1476
Structure-activity relationships of novel 2-substituted quinazoline antibacterial agents.
@en
P2093
Vickers TA
Wilson-Lingardo L
P304
P356
10.1021/JM9903500
P407
P577
1999-11-01T00:00:00Z