نتایج جستجو برای: lactams

تعداد نتایج: 5234  

2006
ROGER LABIA

I. Amino Acids A. Alkylamino Acids: :-Alkylamino acids, L-proline, L-valine. B. Hydroxyamino Acids: L-Serine, L-threonine, D-allothreonine, L-isoserine. C. Amino-amino Acids: L-2,3-Diaminopropionic acid, L-2,4-diaminobutyric acid. D. Carboxyamino Acids: L-Aspartic acid, 3-amino-pentanedioic acids. E. Thioamino Acids: D-Penicillamine, DOr L-methylcysteine, L-cysteine, L-methionine. F. Amido-amin...

Journal: :Synlett 2021

Abstract Bicyclic lactams can be prepared from diethyl aminomalonate and substituted benzaldehydes by formation of a dimerised imidazolidine cycloadduct followed Dieckmann ring closure. The resulting N,N-heterocycles are metal-chelating but show no antibacterial activity.

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه شیراز - دانشکده علوم 1386

چکیده ندارد.

Journal: :Journal of medicinal chemistry 2000
W Lee Z H Li S Vakulenko S Mobashery

Sodium 7beta-[(R)-2-(N(b)()-o-nitrobenzyloxycarbonyl)hydrazino-3-pheny lpropa namido]cephalosporanate (1) is described as a new type of beta-lactam antibiotic, which undergoes light-induced destruction of its beta-lactam moiety and hence becomes biologically inactive. This type of antibiotic holds the promise of self-destruction over a number of hours of exposure to light, so that it would not ...

Journal: :Journal of bacteriology 1972
C H O'Callaghan S M Kirby A Morris R E Waller R E Duncombe

The hydrolysis of two cephalosporins by three different beta-lactamases has been studied. Each enzyme caused a decrease in ultraviolet absorption, a loss of biological activity, and the release of the leaving group from the 3-position. The changes occurred at the same rate and to the same extent with each enzyme, and it is inferred that the loss of the leaving group is a consequence of, and not...

Journal: :Physical chemistry chemical physics : PCCP 2010
Alessandro Bongini Mauro Panunzio Alessandro Venturini

The two competing mechanisms in the reaction of 3-trialkylsilyloxy-2-aza-1,3 dienes to form beta-lactams through a [2+2] electrocyclic ring closure or tetrahydrooxazinan-4-ones via a [4+2] hetero-Diels-Alder reaction were studied using Density Functional computations. Although the [2+2] and [4+2] mechanisms are typical of dienes, their competition, starting from the same diene intermediate, has...

Journal: :Canada communicable disease report = Releve des maladies transmissibles au Canada 2007
L Larcombe J Waruk J Schellenberg M Ormond

The global spread of community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) since the mid-1990s is a major public health concern. The epidemiology of CA-MRSA differs from that of health-care-associated MRSA (HCA-MRSA), and this is reflected at the genetic level. Resistance to beta-lactams is encoded in the mecA gene, which is carried, along with resistance determinants for o...

Journal: :Antimicrobial agents and chemotherapy 2001
C Betriu A Sánchez M L Palau M Gómez J J Picazo

The activity of MK-0826, a new carbapenem, against 309 Bacteroides fragilis group strains was investigated and compared with that of 11 other beta-lactam and 5 non-beta-lactam agents. MK-0826 showed excellent activity (MICs ranged from < or =0.06 to 4 microg/ml). The new carbapenem may be useful in the treatment of mixed anaerobic infections involving B. fragilis group strains.

2006
Geoffrey W. Coombs Julie C. Pearson Frances G. O'Brien Ronan J. Murray Warren B. Grubb Keryn J. Christiansen

Community-associated methicillin-resistant Staphylococcus aureus (MRSA) was first reported in Western Australia in the early 1990s from indigenous peoples living in remote areas. Although a statewide policy of screening all hospital patients and staff who have lived outside the state for MRSA has prevented the establishment of multidrug-resistant epidemic MRSA, the policy has not prevented SCCm...

Journal: :Organic letters 2000
A M Hafez A E Taggi H Wack W J Drury T Lectka

[structure] A catalytic asymmetric reaction process was designed involving the use of solid-phase reagents and catalysts that constitute the packing of a series of "reaction columns". This process was applied to the catalytic asymmetric synthesis of beta-lactams, yielding pure product after crystallization with exceptional enantio- and diastereoselectivity.

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