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Nitrofuranes

ANTIBACTERIALAGENTSSYNTTiETIC - NITROFURANS] (Vol2) 3-[(5-Nitro-2-furanyl)methyleneamino]-2-oxazolidinone... [Pg.679]

Alkylfurans, halofurans, alkoxyfurans, furfuryl ester and ethers, and furfural diacetate [613-75-2] behave similarly. Furans containing electron withdrawing constituents, for example, furfural, 2-furoic acid, and nitrofurans, fail as dienes even with very strong dienophiles. [Pg.74]

Chemically synthesized antimicrobials used in animal and poultry feeds include arsenicals, eg, arsanilic acid [98-50-0] sodium arsanilate [127-85-5] and roxarsone [121-19-7]-, sulfa dmgs, eg, sulfadimethoxine [122-11-2], sulfamethazine [57-68-1], and sulfathiazole [72-14-0]-, carbadox [6804-07-5]-, and nitrofurans, eg, furazoHdone [67 5-8] and nitrofurazone [59-87-0] (see Antibacterial agents, synthetic Antiparasitic agents). [Pg.410]

The nitrofurans encompass a class of synthetic antibacterials characterized by the 5-nitro-2-furanyl group ... [Pg.459]

The antimicrobial activity of this class of compounds was first reported ia 1943 (1) and this finding was described iadependendy four years later (2). After iavestigation of several derivatives, it was concluded that the 5-nitro function was responsible for the observed antimicrobial activity (3). These preliminary findings focused attention on this area of research and as a result, several thousand nitrofurans have been prepared, and thousands of articles have been prepared, and thousands of articles have been pubUshed describiag the extensive efforts ia these areas. [Pg.460]

Although in vitro mutagenicity tests suggest that some nitrofurans in general provoke a positive response, use of in vivo mammalian systems has produced equivocal or negative results. [Pg.460]

These three nitrofurans have been used therapeutically for over 30 years with no reports of human neoplasia and the relevance of the animal findings to short term therapy in humans has not been estabUshed. [Pg.460]

Most commerciali2ed nitrofurans are derived from 5-nitro-2-furancarboxaldehyde [698-63-5] or the corresponding diacetate. [Pg.460]


See other pages where Nitrofuranes is mentioned: [Pg.569]    [Pg.65]    [Pg.236]    [Pg.427]    [Pg.427]    [Pg.427]    [Pg.427]    [Pg.428]    [Pg.673]    [Pg.673]    [Pg.673]    [Pg.673]    [Pg.673]    [Pg.674]    [Pg.679]    [Pg.679]    [Pg.679]    [Pg.679]    [Pg.679]    [Pg.679]    [Pg.679]    [Pg.679]    [Pg.679]    [Pg.679]    [Pg.679]    [Pg.684]    [Pg.719]    [Pg.73]    [Pg.450]    [Pg.459]    [Pg.459]    [Pg.459]    [Pg.460]    [Pg.460]    [Pg.460]    [Pg.460]    [Pg.461]    [Pg.462]    [Pg.403]    [Pg.264]   
See also in sourсe #XX -- [ Pg.91 ]




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2- Nitrofurans, reduction

2-Formyl-5-nitrofuran

2-Nitrofuran, irradiation

2-Nitrofurans, radicals from

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5-Nitrofuran-2-carbaldehyde

Analysis of Nitrofurans

Analytical determination of nitrofurans

Antibacterial 5-nitrofuran derivative

Antibacterial nitrofurans

Assays of nitrofurans

Bacteriostats nitrofuran derivative

Identification of Nitrofuran Metabolites

Nitrofuran chemical structures

Nitrofuran drugs

Nitrofuran recommendation

Nitrofuran reductase

Nitrofuran vinylogues - the formation of panfuran

Nitrofurans

Nitrofurans

Nitrofurans (chemotherapeutic agents

Nitrofurans antibacterial action

Nitrofurans assays

Nitrofurans confirmation

Nitrofurans detection

Nitrofurans heterocyclic derivatives

Nitrofurans metabolics

Nitrofurans metabolism

Nitrofurans methods

Nitrofurans pharmacology

Nitrofurans stability

Nitrofurans systemic antibacterial

Nitrofurans toxicity

Nitrofurans types

Nitrofurans, analysis

Nitrofurans, list

Nitrofurans, synthesis

Nitrofurans, use

Nucleophilic aromatic substitution 2-nitrofurans

Other types of nitrofurans

Synthesis of nitrofurans

Trypanocidal nitrofurans

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