Base de dados : HANSEN
Pesquisa : CINETICA [Descritor de assunto]
Referências encontradas : 9 [refinar]
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  1 / 9 HANSEN  
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Id:23735
Autor:Lopez-Hurtado, Marcela; Flores-Medina, Saul; Díaz-García, Francisco J; Guerra-Infante, Fernando M
Título:Partial characterization of phagocytic activity in neutrophils of the nine-banded armadillo Dasypus novemcinctus
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Fonte:s.l; s.n; 2005. [7] p. tab.
Descritores:Animais
Tatus/*IM
Atividade Bactericida do Sangue
Quimiotaxia de Leucócito/DE
Endocitose
Escherichia coli/IM
Humanos
In Vitro
Cinética
Hanseníase/IM
Monócitos/IM
N-Formilmetionina Leucil-Fenilalanina/PD
Neutrófilos/DE/*IM
Proteínas Opsonizantes/IM
Fagocitose/*
Localização:BR191.1; 09349/S


  2 / 9 HANSEN  
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Id:18950
Autor:Dhungana, Suraj; Miller, Marvin J; Dong, Li; Ratledge, Colin; Crumbliss, Alvin L
Título:Iron chelation properties of an extracellular siderophore exochelin MN
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Fonte:s.l; s.n; 2003. 10 p. tab, graf.
Resumo:The coordination chemistry of an extracellular siderophore produced by Mycobacterium neoaurum, exochelin MN (ExoMN), is reported along with its pK(a) values, Fe(III) and Fe(II) chelation constants, and aqueous solution speciation as determined by spectrophotometric and potentiometric titration techniques. Exochelin MN is of particular interest as it can efficiently transport iron into pathogenic M. leprae, which is responsible for leprosy, in addition to its own parent cells. The Fe(III) coordination properties of ExoMN are important with respect to understanding the Fe(III) acquisition and uptake mechanism in pathogenic M. leprae, as the siderophores from this organism are very difficult to isolate. Exochelin MN has two hydroxamic acid groups and an unusual threo-beta-hydroxy-l-histidine available for Fe(III) chelation. The presence of threo-beta-hydroxy-l-histidine gives rise to a unique mode of Fe(III) coordination. The pK(a) values for the two hydroxamic acid moieties, the histidine imidazole ring and the alkylammonium groups on ExoMN, correspond well with the literature values for these moieties. Proton-dependent Fe(III)- and Fe(II)-ExoMN equilibrium constants were determined using a model involving sequential protonation of the Fe(III)- and Fe(II)-ExoMN complexes. These data were used to develop a model whereby deprotonation reactions on the surface of the complex in the second coordination shell result in first coordination shell isomerization. The overall formation constants were calculated: log beta(110) = 39.12 for Fe(III)-ExoMN and 16.7 for Fe(II)-ExoMN. The calculated pFe value of 31.1 is one of the highest among all siderophores and their synthetic analogues and indicates that ExoMN is thermodynamically capable of removing Fe(III) from transferrin. The E(1/2) for the Fe(III)ExoMN/Fe(II)ExoMN(-) couple was determined to be -595 mV from quasi-reversible cyclic voltammograms at pH = 10.8, and the pH-dependent E(1/2) profile was used to determine the Fe(II)-ExoMN protonation constants. (AU).
Descritores:CONCENTRACAO DE IONS DE HIDROGÊNIO
COMPOSTOS FERRICOS/quim
COMPOSTOS FERROSOS/quim
AGENTES QUELANTES DE FERRO/quim
CINETICA
MYCOBACTERIUM/quim
PEPTIDIOS CÍCLICOS/quim
POTENCIOMETRIA
ESPECTROFOTOMETRIA ULTRAVIOLETA
Limites:SUPPORT, U.S. GOV'T, NON-P.H.S.
SUPPORT, U.S. GOV'T, P.H.S.
Meio Eletrônico: - .
Localização:BR191.1; 09081/s


  3 / 9 HANSEN  
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Id:18179
Autor:Shepard, Charles C; Walker, Laura L; Van Landingham, Rosalind M; Redus, Martha A
Título:Kinetic testing of drugs against Mycobacterium leprae in mice. Activity of cephaloridine, rifampin, streptovaricin, vadrine, and viomycin
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Fonte:s.l; s.n; jul. 1971. 5 p. tab, graf.
Resumo:A series of drugs that had been found active against Mycobacterium leprae in mice by the continous method of drug administration was tested by the kinetic method. Vadrine and vyomivin were found inactive. Cephaloridine, streptovaricin, and rifampin gave bactericidal-type results. In a second experiment, rifampin was found to have distinct bactericidal effect when given for only 2 days. The plasma levels of rifampin that were associated with bactericidal effect in mice were in the range reported for man receiving acceptable dosages of rifampin. Cephaloridine and, especially, rifampin merit further investigation in clinical trials in leprosy patients, either as single drugs or in combination with other active drugs. The combination of rifampin and dapsone (DDS) or acedapsone (DADDS) appear to provide the advantages of tboth drugs.(AU).
Descritores:ANTIMALARICOS/admin
DAPSONA/admin
INJECOES SUBCUTÂNEAS
HANSENIASE/quimioter
MYCOBACTERIUM LEPRAE/ef drogas
MYCOBACTERIUM LEPRAE/cresc
RIFAMPINA/admin
RIFAMPINA/sangue
VIOMICINA/admin
DIETA
 ESTUDOS DE AVALIACAO
 CINETICA
 MALARIA/sangue
 OXIDIAZOIS/admin
 PIRIDINAS/admin
 ACIDOS SALICILICOS/admin
 ESTREPTOVARICINA/admin
Limites:ANIMAL
CAMUNDONGOS
Meio Eletrônico: - .
Localização:BR191.1; 02305/s


  4 / 9 HANSEN  
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Id:18083
Autor:Khanolkar, S. R
Título:Preliminary studies of the metabolic activity of purified suspensions of Mycobacterium leprae
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Fonte:s.l; s.n; feb. 1982. 3 p. graf.
Resumo:Mycobacterium leprae isolated from armadillo tissue incorporated radioactivity from D-(14C)glucose and (14C)protein hydrolysate. In the presence of glucose, the rate of incorporation of (14C)protein hydrolysate was increased. Uptake of glucose was inhibited by 2-deoxy-D-glucose and sodium azide; that of the amino acids was inhibited by puromycin and chloramphenicol and, weakly, by cycloheximide.(AU).
Descritores:AMINOACIDOS/metab
PROTEINAS DE BACTERIAS/bios
CINETICA
TRANSPORTE BIOLOGICO
AZIDA SODICA
PUROMICINA/farmacol
MYCOBACTERIUM LEPRAE/metab
CLORANFENICOL/farmacol
Limites:SUPPORT, NON-U.S. GOV'T
Meio Eletrônico: - .
Localização:BR191.1; 00904/s


  5 / 9 HANSEN  
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Id:17921
Autor:Sanfilippo, A; Della Bruna, C; Marsili, L; Morvillo, E; Pasqualucci, C. R; Schioppacassi, G; Ungheri, D
Título:Biological activity of a new class of rifamycins. Spiro-piperidyl-rifamycins
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Fonte:s.l; s.n; Oct. 1980. 6 p. tab.
Resumo:The biological properties of spiro-piperidyl-rifamycins, a new class of rifamycin antibiotics, are described. In these derivatives the positions 3 and 4 have been incorporated into an imidazolyl ring bearing a spiro-piperidyl group N substituted with linear and branched aliphatic chains. The in vitro antibacterial activity against Staphylococcus aureus and Mycobacterium tuberculosis increases with the number of the carbon atoms in the linera side chain, whereas the inhibitory effect on Escherichia coli is lowered. The antibacterial activity is only marginally affected by branching of the side chain. In vivo (experimental infections of mice) the optimal therapeutic activity against M. tuberculosis is shown by compounds bearing 3 approximately 5 carbon atoms as a linear or branched side chain; in comparison with rifampicin, the potency of these derivatives is 2 approximately 3 times higher. The finding is in a good agreement with the exceptional tissue tropism, which seems to be a favourable property of this group of derivatives.
Descritores:CINETICA
RIFABUTINA
RIFAMICINAS/metab
RIFAMICINAS/farmacol
DISTRIBUICAO TECIDUAL
INFECCOES BACTERIANAS/quimioter
BACTERIAS/ef drogas
Limites:ANIMAL
FEMININO
CAMUNDONGOS
Meio Eletrônico: - .
Localização:BR191.1; 00687/s


  6 / 9 HANSEN  
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Id:14150
Autor:Birdi, Tannaz J; D'Souza, Sushila; Antia, Noshir H
Título:Expression of mycobacterial antigens on murine dissociated Schwann cells infected with Mycobacterium leprae
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Fonte:s.l; s.n; 1997. 5 p. graf.
Descritores:ANTICORPOS ANTIBACTÉRIAS
ANTIMICOTICOS
ANTIGENOS DE BACTÉRIAS
ANTIGENOS DE BACTÉRIAS
ANTIMALARICOS
MEMBRANA CELULAR
CLOROQUINA
ELISA
INTERFERON RECOMBINANTE GAMA
CINÉTICA
HANSENIASE
HANSENIASE
CAMUNDONGOS
MONENSIN
MYCOBACTERIUM LEPRAE
CÉLULAS DE SCHWANN
Limites:ANIMAL
Localização:BR191.1; 07116/s


  7 / 9 HANSEN  
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Id:13985
Autor:Fujita, Mayumi; Miyachi, Yoshiki; Nakata, Koh; Imamura, Sadao
Título:Appearance of gamma delta T cell receptor-positive cells following alpha beta T cell receptor-positive cells in the lepromin reaction of human skin
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Fonte:s.l; s.n; 1993. 6 p. ilus, tab, graf.
Descritores:IMUNOFLUORESCENCIA
CINÉTICA
ANTIGENO DE MITSUDA
HANSENIASE
MYCOBACTERIUM LEPRAE
RECEPTORES PARA ANTIGENOS DE CÉLULAS T ALFA-BETA
RECEPTORES PARA ANTIGENOS DE CÉLULAS T GAMA-DELTA
RECEPTORES PARA ANTIGENOS DE CÉLULAS T GAMA-DELTA
PELE
PELE
SUB-POPULAÇOES DE LINFOCITOS T
Localização:BR191.1; 06631/s


  8 / 9 HANSEN  
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Id:13265
Autor:Gelber, Robert H
Título:The activity of amoxicillin plus clavulanic acid against Mycobacterium leprae in mice
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Fonte:s.l; s.n; 1991. 4 p. tab, graf.
Descritores:AMOXICILINA
AMOXICILINA
ANTIBIOTICOS COMBINADOS
ANTIBIOTICOS COMBINADOS
ACIDOS CLAVULANICOS
ACIDOS CLAVULANICOS
DAPSONA
DAPSONA
QUIMIOTERAPIA COMBINADA
KANAMICINA
KANAMICINA
CINÉTICA
HANSENIASE
CAMUNDONGOS
MYCOBACTERIUM LEPRAE
RIFAMPINA
RIFAMPINA
COMBINACAO AMOXICILINA-CLAVULANATO DE POTASSIO
Localização:BR191.1; 06235/s


  9 / 9 HANSEN  
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Id:5694
Autor:Kulkarni, V. M; Seydel, J. K
Título:Inhibitory activity and mode of action of diaminodiphenysulfone in cell-free folate-synthesizing systems prepared from Mycobacterium lufu and Mycobacterium leprae: a comparison
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Fonte:s.l; s.n; 1983. 10 p. graf.
Descritores:HANSENIASE
MYCOBACTERIUM
MYCOBACTERIUM
MYCOBACTERIUM LEPRAE
MYCOBACTERIUM LEPRAE
AUTO-RADIOGRAFIA
DAPSONA
ACIDO FOLICO
CINÉTICA
ACIDO 4-AMINOBENZOICO
Localização:BR191.1; 02659/s



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