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sulphoxide (5% v/v DMSO) and groups treated with methanol extracts of DM and MW . The groups treated with DM and MW were given graded dosages of 100, 200 and 400 mg/kg of each methanol extract, respectively. To determine the effects of the vehicle on

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terpenoids were all obtained as white amorphous powder. Dihydrokaempferol ( 1 ): ESI–MS, m/z 311.3 [M + Na] + . 1 H-NMR (DMSO- d 6 , 400 MHz) δ : 4.58 (1H, d, J = 11.2 Hz, H-3), 5.04 (1H, d, J = 11.2 Hz, H-2), 5.86 (1H, s, H-6), 5.91 (1H, s

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electrolytes in the mixtures of water with N , N -dimetylformamide and dimethylsulfoxide (DMSO) as well as with organic substances which do not contain a non-polar group in their molecules, like formamide and urea, run monotonously within the whole range of

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Acta Chromatographica
Authors: Yuping Shen, Minhui Xu, Peipei Deng, Qinying Gu, Huawu Yin, Guohua Xia, Xiaobin Jia, Huan Yang, and James Tam

electrospray ionization (ESI) mode using a Thermo LXQ HPLC–ion trap–MS instrument via direct injection. 1 H-NMR and 13 C-NMR spectra were obtained by a Bruker AV-400 spectrometer using DMSO- d 6 as solvent. A Waters Acquity UPLC system was used for

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Materials, synthesis, and analysis 4,4′-Bipyridine, CCl 3 COOH, CHBr 2 COOH, Y 2 O 3 , La 2 O 3 , dimethylsulfoxide (DMSO), dimethylformamide (DMF), and methanol (MeOH) (anhydrous) p.a. were obtained from Aldrich and Lab-Scan. Water solutions of

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(Heteronuclear Multiple Bond Correlation) spectra were obtained using a pulse sequence supplied from Varian Mecauy 300 MHz spectrometer ( 1 H, 300 MHz and 13 C, 75 MHz, in deuterated dimethylsulphoxide [DMSO- d 6 ]). Chemical shifts ( δ ) were given in values

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Biologia Futura
Authors: Gergely Sámuel Bartha, Gergő Tóth, Péter Horváth, Eszter Kiss, Nóra Papp, and Monika Kerényi

measured and then chloroform, ethyl acetate, and butanol were used for further extraction. Dried residues were dissolved with dimethyl sulfoxide (DMSO; Sigma-Aldrich). Further dilutions were performed in Mueller–Hinton broth to reach the appropriate

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Acta Chromatographica
Authors: Su-su Bao, Jian Wen, Teng-hui Liu, Bo-wen Zhang, Chen-chen Wang, and Guo-xin Hu

the Laboratory Animal Center of Wenzhou Medical University (Wen-Zhou, China) to perform the pharmacokinetic study of olmutinib. All rats were fasted overnight. Olmutinib was dissolved in dimethyl sulfoxide (DMSO) (modicum, since DMSO is toxic) and

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. 2017; 10: 403–412. 10.2147/DMSO.S141235 . eCollection 2017. 44 Chis BA, Fodor D. Acute pancreatitis during GLP-1 receptor agonist treatment. A case report. Clujul Med. 2018; 91

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sulfoxide (DMSO)] were used. The concentration of DMSO in the tissue bath was always kept below 0.4%. Phenylephrine and acetylcholine were obtained from Sigma-Aldrich (St. Louis, MO, USA). Cilostazol and atorvastatin were kindly provided by Abdi İbrahim Drug

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