Inhibition of smooth muscle contractility by indole and some indole compounds.
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Indoles↗
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Identification of clinical isolates of indole-positive and indole-negative Klebsiella spp.
Biochemical methods employed to classify bacterial species have limitations and may have contributed to the taxonomic complexity recently reported for the genus Klebsiella. The objective of the present study was to apply a simple biochemical test panel to classify a collection of human Klebsiella isolates. We found that with only three additional tests, it is possible to place most isolates in a defined species. Analysis of a 512-bp sequence of the rpoB gene was used as the reference. A total of 16 conventional and 4 supplementary tests were used to evaluate 122 recent isolates identified as Klebsiella from 120 patients, isolated at the clinical laboratory of a university hospital in Minas Gerais, Brazil. Of these, 102 (84%) isolates were identified as Klebsiella pneumoniae or Klebsiella variicola, 19 (15%) as Klebsiella oxytoca, and 1 (1%) as Raoultella planticola. Enterobacterial repetitive intergenic consensus-PCR typing revealed a diversity of genotypes. rpoB gene sequencing confirmed the phenotypic identification and detected five K. variicola isolates among the K. pneumoniae/K. variicola group. Three additional tests that include growth at 10 degrees C and histamine and d-melezitose assimilation should be considered essential tests for the typing of Klebsiella isolates.
Bacterial Proteins↗
Indole-acetic acid, 3-methyl indole and type 2 pneumonocyte hyperplasia in a proliferative alveolitis of cattle.
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Animals↗
Indoles and auxins. X. 2,4-dinitrophenylsulfenyl chloride, a reagent for separation and identification of naturally occurring indoles.
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Chromatography, Thin Layer↗
Body fluid indoles of normal and mentally-ill subjects. I. Preliminary survey of the occurrence of some urinary indoles.
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Body Fluids↗
Studies on indole series. I. Studies on the synthesis of optically active indole derivatives.
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Indoles↗
Furo[3,2-b]indole derivatives. I. Synthesis and analgesic and anti-inflammatory activities of 4,6-disubstituted-furo[3,2-b]indole-2-carboxamide derivatives.
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Animals↗
Studies on fused indoles. II. Structural modifications and analgesic activity of 4-aminomethyltetrahydrothiopyrano[2,3-b]indoles.
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Analgesics↗
Furo[3,2-b]indole derivatives. II. Synthesis and analgesic and anti-inflammatory activities of 4-alkoxycarbonyl-2-morpholinocarbonylfuro[3,2-b]indole derivatives.
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Animals↗
Furo[3,2-b]indole derivatives. III. Structure-activity studies of 4,6-disubstituted N-(3-piperidinopropyl)furo[3,2-b]indole-2-carboxamide derivatives for analgesic and antiinflammatory activities.
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Animals↗
Pharmacological studies of furo[3,2-b]indole derivatives. III. Correlation between analgesic effect and effect on central nervous system of N-(3-piperidinopropyl)-4-methyl-6-trifluoromethyl furo[3,2-b]indole-2-carboxamide (FI-302) in mice.
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Aggression↗
Furo[3,2-b]indole derivatives. V. Synthesis and structure-activity studies of 4-substituted 2-(4-methylpiperazinylcarbonyl)-6-trifluoromethylfuro[3,2- b]indole derivatives with analgesic and antiinflammatory activities.
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Animals↗
[Studies on indole derivatives. VI. Synthesis of 2-oxo-4-methylthio-2H-pyrano[2,3-b]-indole derivatives and their reaction].
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Chemical Phenomena↗
[Studies on indole derivatives. VII. Diels-Alder reaction of 2-oxo-4-methylthiopyrano-[2,3-b]-indole derivatives].
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Chemical Phenomena↗
[Studies on indole derivatives. 8. Synthesis of thieno (2,3-b)indole derivatives and their reactions].
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Chemical Phenomena↗
[Studies on indole derivatives. X. Synthesis of methyl indole dithiocarboxylates and reaction with amines].
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Amines↗
[Studies on indole derivatives. IX. Synthesis of 1,2-dithiolo[3,4-b]-indole-3-thione derivatives and their reactions].
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Amines↗
[Studies on indole derivatives. XII. Reaction of indole-2-carboxylic acid derivatives with carbon disulfide].
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Carbon Disulfide↗