Boronic Acids
Mostrando 1-12 de 12 artigos, teses e dissertações.
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1. New α-Hydroxy-1,2,3-triazoles and 9H-Fluorenes-1,2,3-triazoles: Synthesis and Evaluation as Glycine Transporter 1 Inhibitors
Two series of new compounds containing 1,2,3-triazole moiety were designed as putative GlyT1 inhibitors aiming the discovery of new hits with activity in cognitive disorders. 1,4-Disubstituted α-hydroxy-1,2,3-triazoles were obtained as racemates in moderate to good yields by the copper-catalyzed azide-alkyne cycloaddition (CuAAC) reaction (click chemistry)
J. Braz. Chem. Soc.. Publicado em: 2020-06
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2. Estratégias para estudo das correlações de energia livre em acoplamento aril-aril de Suzuki: elucidando ciclos catalíticos através da equação de Hammett
The present work deals with the study of the correlation of free-energy developed in a catalytic system for Suzuki coupling, by way of the Hammett equation. The system presents NCP pincer palladacycle 1 as a catalyst precursor, which proved to be very efficient in the coupling of various aryl boronic acids with aryl halides in previous studies. Thus, the art
Química Nova. Publicado em: 2012
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3. Palladium catalyzed Suzuki cross-coupling of 3-iodo-2-(methylthio)-benzo[b]furan derivatives: synthesis of 3-aryl-2-(methylthio)benzo[b]furans
Neste trabalho desenvolvemos um método seletivo e eficiente para a síntese de derivados de 3-aril-2-(tiometil)-benzo[b]furanos, via reação de acoplamento com ácidos borônicos, catalisada por paládio. As condições reacionais usadas foram brandas e compatíveis com ácidos borônicos contendo substituintes retiradores, doadores de elétrons ou neutros
Journal of the Brazilian Chemical Society. Publicado em: 2010
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4. Detecção de analitos neutros e aniônicos através do uso de sensores cromogênicos baseados na competição de uma merocianina solvatocrômica e do substrato por uma unidade receptora
Este trabalho apresenta o desenvolvimento de sensores cromogênicos para espécies neutras e aniônicas, através da interação uma merocianina solvatocrômica (merocianina de Brooker, MB) com diferentes receptores (α-, β-, γ-, hidroxipropil-β, metil-β-ciclodextrina e ácido fenil borônico). A interação não covalente de ciclodex
Publicado em: 2007
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5. Avaliação in silico de inserções com boro em moléculas com atividade farmacológica
The growth of leukemia incidence, cardiac problems and global AIDS epidemic, with appearing of resistant forms of HIV, stimulated the search of new medications. In this work, we investigated new active pharmacologic compounds based on boron including the anti-HIV drugs. The interest in boron compounds with pharmacologic activity has increased in recent years
Publicado em: 2006
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6. Dimeric boronates derived from the reaction of schiff bases and boronic acids
A síntese one-pot de complexos diméricos de boro é descrita. Os compostos foram obtidos pela reação de bases de Schiff (ligantes tridentados) com ácido trans-beta-fenilvinilborônico, ácido 3-tiofeninoborônico e ácido metilborônico. A construção das estruturas diméricas é favorecida pela presença de ligações de coordenação N-> B intramolec
Journal of the Brazilian Chemical Society. Publicado em: 2005-06
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7. Use of Phenylboronic Acids to Investigate Boron Function in Plants. Possible Role of Boron in Transvacuolar Cytoplasmic Strands and Cell-to-Wall Adhesion
The only defined physiological role of boron in plants is as a cross-linking molecule involving reversible covalent bonds with cis-diols on either side of borate. Boronic acids, which form the same reversible bonds with cis-diols but cannot cross-link two molecules, were used to selectively disrupt boron function in plants. In cultured tobacco (Nicotiana tab
American Society of Plant Biologists.
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8. Crystal versus solution structure of enzymes: NMR spectroscopy of a peptide boronic acid-serine protease complex in the crystalline state.
The effectiveness of boronic acids as inhibitors of serine proteases has been widely ascribed to the ability of the boronyl group to form a tetrahedral adduct with the active-site serine that closely mimics the putative tetrahedral intermediate or transition state formed with substrates. However, recent 15N NMR studies of alpha-lytic protease (EC 3.4.21.12)
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9. Catabolism of Arylboronic Acids by Arthrobacter nicotinovorans Strain PBA
Arthrobacter sp. strain PBA metabolized phenylboronic acid to phenol. The oxygen atom in phenol was shown to be derived from the atmosphere using 18O2. 1-Naphthalene-, 2-naphthalene-, 3-cyanophenyl-, 2,5-fluorophenyl-, and 3-thiophene-boronic acids were also transformed to monooxygenated products. The oxygen atom in the product was bonded to the ring carbon
American Society for Microbiology.
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10. Inhibition of dipeptidyl aminopeptidase IV (DP-IV) by Xaa-boroPro dipeptides and use of these inhibitors to examine the role of DP-IV in T-cell function.
Dipeptidyl peptidase IV (DP-IV; dipeptidyl-peptide hydrolase, EC 3.4.14.5) is a serine protease with a specificity for cleaving Xaa-Pro dipeptides from polypeptides and proteins. It is found in a variety of mammalian cells and tissues, including those of lymphoid origin where it is found specifically on the surface of CD4+ T cells. Although the functional si
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11. Purification of Staphylococcus aureus beta-lactamases by using sequential cation-exchange and affinity chromatography.
Boronic acids are active-site inhibitors of serine beta-lactamases, and a phenylboronic acid-agarose affinity column has been used to purify beta-lactamase from crude cell extracts of several bacterial species. We applied phenylboronic acid-agarose chromatography to the purification of Staphylococcus aureus beta-lactamase. Two factors interfered with the suc
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12. A serine peptidase responsible for the inactivation of endogenous cholecystokinin in brain.
A serine endopeptidase was characterized as a major inactivating enzyme for endogenous cholecystokinin (CCK) in brain. CCK-8 released by depolarization of slices of rat cerebral cortex, as measured by its immunoreactivity (CCK-ir), undergoes extensive degradation (approximately 85% of the amount released) before reaching the incubation medium. However, recov