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111.
112.
Synthesis and in vitro antimicrobial screening of new pyrano[4,3-b]pyrane derivatives of 1H-pyrazole
A new series of pyrano[4,3-b]pyrane 4a-l bearing 1H-pyrazole has been synthesized by one pot base catalyzed cyclocondensation reaction of 1H-pyrazole-4-carbaldehyde la-1,malononitrile 2 and 4-hydroxy-6-methylpyrone 3.All the synthesized compounds were screened against six bacterial pathogens,namely B.subtilis,C.tetani,S.pneumoniae,S.typhi,V.cholerae, E.coli and antifungal activity against,two fungal pathogens,A.fumigatus and C.albicans using broth microdilution MIC method. Some of the compounds are found to be equipotent or more potent than that of commercial drugs,against most of employed strains. 相似文献
113.
Oxidation of Antitubercular Drug Isoniazid by a Lipopathic Oxidant,Cetyltrimethylammonium Dichromate: A Mechanistic Study
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The oxidation of an antitubercular drug isoniazid by a lipopathic oxidant cetyltrimethylammonium dichromate (CTADC) in a nonpolar medium generates isonicotinic acid both in the presence and the absence of acetic acid. The conventional UV–vis spectrophotometric method is used to study the reaction kinetics. The occurrence of the Michaelis–Menten–type kinetics with respect to isoniazid confirms the binding of oxidant and substrate to form a complex before the rate‐determining step. The existence of the inverse solvent kinetic isotope effect, k(H2O)/ k(D2O) = 0.7, in an acid‐catalyzed reaction proposes a multistep reaction mechanism. A decrease in the rate constant with an increase in [CTADC] reveals the formation of reverse micellar–type aggregates of CTADC in nonpolar solvents. In the presence of different ionic and nonionic surfactants, CTADC forms mixed aggregates and controls the reaction due to the charge on the interface and also due to partition of oxidant and substrate in two different domains. High negative entropy of activation (ΔS? = –145 and –159 J K?1 mol?1 in the absence and presence of acetic acid) proposes a more ordered and highly solvated transition state than the reactants. Furthermore, the solvent polarity‐reactivity relationship reveals (i) the presence of less polar and less ionic transition state compared to the reactants during the oxidation, (ii) differential contribution from nonpolar and dipolar aprotic solvents toward the reaction process, and (iii) the existence of polarity/hydrophobic switch at log P = 0.73. A suitable mechanism has been proposed on the basis of experimental results. These results may provide insight into the mechanism of isoniazid oxidation in hydrophobic environment and may assist in understanding the drug resistance in different location. 相似文献
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A. L. Roes L. B. Tabak L. Shen E. Nieuwlaar M. K. Patel 《Journal of nanoparticle research》2010,12(6):2011-2028
The goal of our study was to investigate the potential benefits of reinforcing polymer matrices with nanoobjects for structural applications by looking at both the mechanical properties and environmental impacts. For determining the mechanical properties, we applied the material indices defined by Ashby for stiffness and strength. For the calculation of environmental impacts, we applied the life cycle assessment methodology, focusing on non-renewable energy use (NREU). NREU has shown to be a good indicator also for other environmental impacts. We then divided the NREU by the appropriate Ashby index to obtain the ‘functionality-based NREU’. We studied 23 different nanocomposites, based on thermoplastic and thermosetting polymer matrices and organophilic montmorillonite, silica, carbon nanotubes (single-walled and multiwalled) and calcium carbonate as filler. For 17 of these, we saw a decrease of the functionality-based NREU with increasing filler content. We draw the conclusion that the use of nanoobjects as filler can have benefits from both an environmental point of view and with respect to mechanical properties. 相似文献
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C. P. Bhasin J. P. Patel M. L. Desai 《Phosphorus, sulfur, and silicon and the related elements》2013,188(10):2509-2524
Dialkyldithiophosphate derivatives of macrocyclic complexes of Pb(II), having N2S2 potential donors, of the general formula, [Pb(L)S2P(OR)2] (where L = macrocyclic ligands L1, L2, L3, L4 & L5 and R = CH3-, C3H7 n- & C3H7 i-) have been Synthesized from the reactions of [Pb(L)X2] (where X = Cl, NO3, or CH3COO) with sodium dialkyl dithiophosphates in 1:2 molar ratios in THF. Fifteen new derivatives have been synthesized by the combination of five macrocyclic complexes of 14–20 member rings with three different types of dialkyldithiophosphate. These compounds have been characterized by elemental analysis, molar conductance, molecular weight determination, IR, 1H NMR, 13C, and 31P NMR. Molecular weight determinations of these complexes indicate their monomeric nature. An octahedral structure is proposed. 相似文献
119.
Amit C. Patel Dharmesh H. Mahajan Kishor H. Chikhalia 《Phosphorus, sulfur, and silicon and the related elements》2013,188(2):368-376
A new series of 2-(coumarin-3-yl)-5-mercapto-1,3,4-oxadiazoles based on various aryl thiourea/ureas incorporating a 1,3,5-s-triazine moiety is reported. The components of this series have been obtained by the reaction of cyanuric chloride (1) with 2-(coumarin-3-yl)-5-mercapto-1,3,4-oxadiazole (2). The prepared 2-{(coumarin-3-yl-1,3,4-oxadiazolyl)-5-thio}-4,6-dichloro-s-triazine (3) was subsequently treated with morpholine (4) to form 2-{(coumarin-3-yl-1,3,4-oxadiazolyl)-5-thio}-4-(morpholino)-6-chloro-s-triazine (5). This was further treated with various substituted aryl urea/thioureas (6a–k/7a–k) to afford the title compounds 8a–k and 9a–k, which were and tested for their antibacterial activity (MIC) against different microorganisms. The structures of the novel synthesized compound have been established on the basis of 1H NMR and FT-IR data together with elemental analysis. Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file. 相似文献
120.
Copolymers (PUF) were synthesized by the condensation of p-hydroxybenzoic acid (P), urea (U), and formaldehyde (F), in the presence of different acidic catalysts and using varied molar ratios of reacting monomers. One of the copolymers having the highest molecular weight was fractionated. Copolymer compositions have been determined on the basis of their elemental analysis and conductometric titrations in the nonaqueous phase. Molecular weights (Mn) have been estimated by VPO. Copolymer prepared by using the stoichiometric properties of the monomers and HCI as catalyst furnished the highest molecular weight (Mn). The viscosity measurements carried out in DMF indicate normal behavior. TGA and DSC data were analyzed to compare the relative thermal stability and estimate the characteristic parameters. IR spectra were studied to elucidate the structure. Chelation ion-exchange properties have also been studied employing the batch equilibration method. The order of selectivity of metal ions by the copolymers is UO2 2+ > Fe3+ >Cu2+ > Co2+. 相似文献