نتایج جستجو برای: nn dichloropolystyrene sulfonamide

تعداد نتایج: 13852  

2001
Richard J. S. Baerends Grietje J. Sulter Thomas W. Jeffries James M. Cregg Marten Veenhuis

Richard J. S. Baerends,{, Grietje J. Sulter, Thomas W. Jeffries, James M. Cregg and Marten Veenhuis* 1 Eukaryotic Microbiology, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, Kerklaan 30, 9751 NN Haren, The Netherlands 2 Institute for Microbial and Biochemical Technology, Forest Products Laboratory, US Department of Agriculture, One Gifford Pinchot Drive, ...

Journal: :Antimicrobial agents and chemotherapy 2003
Désirée E Bennett Mary T Cafferkey

We identified a previously undocumented mutation in the dihydropteroate synthase (folP) gene associated with Neisseria meningitidis sulfonamide resistance. A PCR-based assay to detect this mutation, which is 100% predictive of sulfonamide resistance, was developed.

2014
Mustafa Durgun Hasan Türkmen Tuncay Tunç Tuncer Hökelek

The title Schiff base compound, C15H17N3O2S, is non-planar with a dihedral angle of 69.88 (4)° between the planes of the benzene rings. In the crystal, pairs of N-H⋯N hydrogen bonds, between the sulfonamide nitro-gen-H atom and the azomethine N atom, link the mol-ecules into inversion dimers, forming R 2 (2)(16) ring motifs. These dimers are linked by N-H⋯O hydrogen bonds, between the sulfonami...

2013
Hakima Chicha El Mostapha Rakib Detlef Geffken Mohamed Saadi Lahcen El Ammari

In the title compound, C17H17N3O3 (.)0.5H2O, the indazole system makes a dihedral angle of 46.19 (8)° with the plane through the benzene ring and is nearly perpendicular to the allyl group, as indicated by the dihedral angle of 81.2 (3)°. In the crystal, the water mol-ecule, disordered over two sites related by an inversion center, forms O-H⋯N bridges between indazole N atoms of two sulfonamide...

Journal: :The Journal of biological chemistry 1982
D S Masters A Meister

Glutamate synthase, isolated in apparently homogeneous form (Mr approximately 265,000) from Saccharomyces cerevisiae after 7500-fold purification, is markedly inhibited by homocysteine sulfonamide. Inhibitions competitive with respect to L-glutamine; the apparent Ki value calculated for L-homocysteine sulfonamide is 3.6 microM; the apparent Km value for L-glutamine is 280 microM. The very high ...

Journal: :Astronomische Nachrichten 1904

Journal: :Journal of Investigative Dermatology 1949

Journal: :Poultry science 2012
T Zhang C G Wang X H Zhong

It is important for the prevention and treatment of colibacillosis to monitor drug resistance in Escherichia coli. To choose effective drugs to prevent and control avian colibacillosis in North China, we investigated the resistance of 164 E. coli isolates (from Beijing, Tianjin, Inner Mongolia, Shanxi, and Hebei regions of China) to commonly used clinical sulfonamide antibiotics using a drug su...

Journal: :The Journal of organic chemistry 2011
Marie Lopez Laurent F Bornaghi Hugues Driguez Sally-Ann Poulsen

A flexible and short synthesis of sulfonamide-bridged di-, tri-, tetra-, and octasaccharide glycomimetics was accomplished by reaction of glycosyl thioacetates with amino sugar substrates. The chemistry to incorporate the sulfonamide linker in place of a native O-glycosidic bond was broadly scoped, allowing access to head-to-head (1↔1) and head-to-tail (1→2), (1→3), (1→4), and (1→6) sulfonamide...

Journal: :The Journal of clinical investigation 1944
W W Spink J J Vivino

A feature of sulfonamide therapy for bacterial infections is that species of bacteria differ in their resistance to the antibacterial action of the compounds. It is also recognized that strains of microorganisms within the same species display variations in susceptibility. A disconcerting and confusing factor associated with chemotherapy, which appears to be assuming increasing clinical signifi...

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