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61.
Venkata Rami Reddy Vaka Jaswanth Kumar Inamadugu Nageswara Rao Pilli Mullangi Ramesh Hussain Reddy Katreddi 《Biomedical chromatography : BMC》2013,27(11):1406-1412
An improved, simple and highly sensitive LC‐MS/MS method has been developed and validated for quantification of febuxostat with 100 μL human plasma using febuxostat‐d7 as an internal standard (IS) according to regulatory guidelines. The analyte and IS were extracted from human plasma via liquid–liquid extraction using diethyl ether. The chromatographic separation was achieved on a Zorbax C18 column using a mixture of acetonitrile and 5 mm ammonium formate (60:40, v/v) as the mobile phase at a flow rate of 0.5 mL/min. The total run time was 5.0 min and the elution of febuxostat and IS occurred at 1.0 and 1.5 min, respectively. A linear response function was established for the range of concentrations 1–6000 ng/mL (r > 0.99). The precursor to product ion transitions monitored for febuxostat and IS were m/z 317.1 → 261.1 and 324.2 → 262.1, respectively. The intra‐ and inter‐day precisions (%RSD) were within 1.29–9.19 and 2.85–7.69%, respectively. The proposed method was successfully applied to pharmacokinetic studies in humans. Copyright © 2013 John Wiley & Sons, Ltd. 相似文献
62.
Shabbir Hussain Saqib Ali Saira Shahzadi Corrado Rizzoli 《Phosphorus, sulfur, and silicon and the related elements》2013,188(6):812-818
Abstract A novel polymeric complex has been synthesized by refluxing disodium acetylene dicarboxylate with tributyltin chloride in dry methanol. The solid-state structure of the complex has been determined by single-crystal X-ray analysis. The tin(IV) metal exhibits distorted trigonal bipyramidal geometry. Each carboxylate group of the ligand acts in a bidentate fashion, linking adjacent metal atoms to produce polymeric chains, which are cross-linked into a three-dimensional network. 相似文献
63.
A. Babulreddy R. V. Hymavathi Md. Manzoor Hussain G. Narayana Swamy 《Journal of heterocyclic chemistry》2013,50(3):727-733
A new class of methyleneamine‐linked bis‐heterocycles that exhibit antimicrobial activity was synthesized. Bromination of 1 followed by condensation with thiourea gave 3 . The reaction of 3 with propargyl bromide in dry toluene under inert atmosphere led to the formation of 4 . Its subsequent reaction with different nitrile oxides using CuSO4.5H2O–sodiumascorbate system in a 2:1 mixture of water and tert‐butyl alcohol yielded the title compounds 6a , 6b , 6c , 6d , 6e , 6f , 6g , 6h , 6i , 6j , 6k , 6l in good yields. The identities of these compounds were confirmed following elemental analysis, IR, 1H, 13C NMR, and mass spectral studies. All the title compounds exhibited pronounced in vitro antibacterial and antifungal activities. 相似文献
64.
A novel approach for the syntheses of carbene adduct 4 is reported. A ring-enlargement strategy was employed for the synthesis of precursors 5 and 6 and established the mechanism of the formation of azulene derivative 6. Synthesis of target precursor 13, a novel precursor for the synthesis of new mesogenic materials, and its various halogenated derivatives (14–16) was carried out. 相似文献
65.
Shreyans K. Jain Samdarshi Meena Asif K. Qazi Aashiq Hussain Sunil K. Bhola Rajendra Kshirsagar Koteppa Pari Anamika Khajuria Abid Hamid R. Uma Shaanker Sandip B. Bharate Ram A. Vishwakarma 《Tetrahedron letters》2013
The chromone alkaloid dysoline (1), a new regioisomer of rohitukine (2) along with rohitukine and rohitukine-N-oxide (3) were isolated from the stem barks of Dysoxylum binectariferum. The structure of dysoline (1) was determined by extensive 2D-NMR studies and the absolute configuration was established by NOESY and CD spectra. Dysoline (1) consisted of a 5,7-dihydroxy-2-methylchromone nucleus substituted with a 2′-hydroxylated N-Me piperidine ring at the C-6 position. Dysoline differs from rohitukine by the position of the piperidine ring on the chromone nucleus. Dysoline displayed promising cytotoxicity in HT1080 fibrosarcoma cells with an IC50 of 0.21 μM, and also displayed significant inhibition of proinflammatory cytokines TNF-α and IL-6. 相似文献
66.
Masrat Maswal Altaf Hussain Pandith Nasrul Islam Aijaz Ahmad Dar 《Journal of solution chemistry》2013,42(7):1374-1392
Co-solubilization of the hydrophobic drugs Carbamezipine (CBZ) and Nifedipine (NFD) by micellar solutions at 25 °C, using two series of polyoxyethylene based nonionic surfactants, was measured and compared. The first series is composed of surfactants with a 12 carbon (C12) hydrophobic chain while the second series had 16 carbon (C16) hydrophobic chains. Experimental results were obtained for solubilization and co-solubilization of CBZ and NFD within the micelles at saturation and quantification was done in terms of the molar solubilization ratio and the micelle–water partition coefficient employing spectrophotometric and tensiometric techniques. The extent of micellar solubilization of CBZ is much greater than NFD. The C12 series of surfactants exhibit higher solubilization capacities for CBZ than the C16 series while the reverse is the case for NFD. Co-solubilization results showed competitive solubilization of the drugs. A synergistic effect on the solubilization of NFD was observed in the presence of CBZ in Brij30 and Brij56 surfactant systems while, in the remaining surfactants, the solubility of NFD was slightly reduced. Since the surfactants used in the present study are either nontoxic or have minimal toxicity, it is expected that they can be employed as drug delivery vehicles for co-administration of the two drugs in vivo. Both from industrial and research points of view, this paper reports a comprehensive study for co-solubilization of differently structured drugs in micellar media. 相似文献
67.
68.
Nusrah Hussain Gustavo Frensch Jiadi Zhang Patrick J. Walsh 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2014,126(14):3767-3771
The combination of aryl bromides, allylbenzene, base and a palladium catalyst usually results in a Heck reaction. Herein we combine these same reagents, but override the Heck pathway by employing a strong base. In the presence of LiN(SiMe3)2, allylbenzene derivatives undergo reversible deprotonation. Transmetalation of the resulting allyllithium intermediate to LPdAr(Br) and reductive elimination provide the 1,1‐diarylprop‐2‐enes, which are not accessible by the Heck reaction. The regioselectivity in this deprotonative cross‐coupling process is catalyst‐controlled and very high. 相似文献
69.
Ismail Muhammad Javed Salma Kazim Muhammad Razaq Abdur Hussain Ejaz Attia-tul-Wahab Ali Sajjad Choudhary Muhammad Iqbal 《Chemistry of Natural Compounds》2022,58(4):637-643
Chemistry of Natural Compounds - One new and seven known secondary metabolites 1–8 were isolated, and the nematocidal and insecticidal activities of major compounds from Tanacetum... 相似文献
70.
We report a label-free and simple approach for the detection of glycoprotein-120 (gp-120) using an aptamer-based liquid crystals (LCs) biosensing platform. The LCs are supported on the surface of a modified glass slide with a suitable amount of B40t77 aptamer, allowing the LCs to be homeotropically aligned. A pronounced topological change was observed on the surface due to a specific interaction between B40t77 and gp-120, which led to the disruption of the homeotropic alignment of LCs. This results in a dark-to-bright transition observed under a polarized optical microscope. With the developed biosensing platform, it was possible to not only identify gp-120, but obtained results were analyzed quantitatively through image analysis. The detection limit of the proposed biosensing platform was investigated to be 0.2 µg/mL of gp-120. Regarding selectivity of the developed platform, no response could be detected when gp-120 was replaced by other proteins, such as bovine serum albumin (BSA), hepatitis A virus capsid protein 1 (Hep A VP1) and immunoglobulin G protein (IgG). Due to attributes such as label-free, high specificity and no need for instrumental read-out, the presented biosensing platform provides the potential to develop a working device for the quick detection of HIV-1 gp-120. 相似文献