Disposition Kinetic of Levofloxacin in Experimentally Induced Febrile Model of Sheep

Patel, Urvesh D.; Patel, Jatin H.; Varia, R.D.; Patel, Harshad B.; Bhavsar, Shailesh K.; Thaker, Aswin M.

doi:10.3923/jpt.2012.11.19

Cited by 45 publications

(65 citation statements)

References 24 publications

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“…Wool yarns dyed with turmeric (Mathur & Gupta, 2003) when subject to different concentration of natural mordant and chromium under identical mordanting conditions, shows similar colour fastness. Application of tulsi leave extract on textiles with or without using metallic salts produces pale to dark green and cream to brown shades with adequate fastness (Patel et al, 2002). Silk (Maulik & Pal, 2005) fabric being mordanted with magnesium sulphate produces lower depth of shade, whereas copper sulphate produces highest depth.…”

Section: Different Mordanting Methods and Application Of Natural Dyesmentioning

confidence: 99%

Dyeing of Textiles with Natural Dyes

Samanta¹,

Konar²

2011

Natural Dyes

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Section: Different Mordanting Methods and Application Of Natural Dyesmentioning

confidence: 99%

Dyeing of Textiles with Natural Dyes

Samanta¹,

Konar²

2011

Natural Dyes

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“…Relative telomerase activity ± SE TDA 7 2.53 ± 0.14 TDA 8 3.21 ± 0.15* TDA 14 2.6 ± 0.14 TDA 15 2.67 ± 0.21 TDA 16 2.16 ± 0.14 Control (vehicle/DMSO) 2.36 ± 0.14 *Statistically different from vehicle (P < 0.05).…”

Section: Selected Compoundsmentioning

confidence: 99%

“…At this stage, triethylamine was very effective in the progress of the reaction by taking the protons in the medium. At the end of all these steps, two starting materials (7,8) were obtained. These starting materials (7,8) were reacted with phenol and thiophenol derivatives as shown in Figure 2 to give the desired compounds (TDA 1−16 ).…”

Section: Chemistrymentioning

confidence: 99%

“…At the end of all these steps, two starting materials (7,8) were obtained. These starting materials (7,8) were reacted with phenol and thiophenol derivatives as shown in Figure 2 to give the desired compounds (TDA 1−16 ). The compounds obtained at the end of each step were carefully separated from the medium and recrystallized to be obtained in perfect purity and packed appropriately.…”

Section: Chemistrymentioning

confidence: 99%

“…The two compounds (7,8) to be used as starting materials were synthesized as shown in Figure 1. In the first step, pyridine-thioamide derivatives were converted to pyridinylthiazole derivatives (1, 2) with ethyl 2- Figure 1.…”

Section: Chemistrymentioning

confidence: 99%

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Synthesis and characterizations of novel thiazolyl-thiadiazole derivatives as telomerase activators

2018

Turk J Chem

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Pyridine-3/4-thiocarboxamide derivatives were used as starting materials for the synthesis of the target compounds. The pyridine-3/4-thiocarboxamide derivatives were reacted with ethyl 2-chloroacetoacetate in ethanol to give the thiazole derivatives (1, 2). The two ethyl thiazole-carboxylate derivatives (1, 2) thus obtained were treated with sodium hydroxide solution and ethanol and converted to carboxylic acids (3, 4). The carboxylic acid derivatives (3, 4) were reacted with thiosemicarbazide in phosphoroxy trichloride and aminothiadiazole rings (5, 6) were formed. Thus, two thiazolyl-thiadiazole amine derivatives (5, 6) were obtained. These two derivatives (5, 6) were converted into two chloroacetamidothiadiazole derivatives (7, 8) by reaction with chloroacetylchloride over the amino group in the presence of triethylamine in acetone. After all these steps, the starting materials (7, 8) needed to reach the target compounds were obtained. With the two derivatives (7, 8) obtained in this last step, phenol and thiophenol derivatives were reacted in acetone in the presence of potassium carbonate. The target compounds, thiazolyl-thiadiazole derivatives (TDA 1−16) , are completely unique and their structure has been elucidated by elemental analysis, IR, NMR, and MS spectral data. After all these synthesis steps, telomerase activity studies were performed on the target compounds obtained. For this purpose, a PCR ELISA-based TRAP method was used on the heart of zebrafish. According to the enzyme assay results, derivative TDA 8 has shown an increase of telomerase enzyme activity.

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Resins IV: Preparation and characterization of terpolymer resins prepared from biphenol, thiourea and formaldehyde

Jadhao

Paliwal

Bhave

2010

J of Applied Polymer Sci

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Terpolymer resins (BPhThF) were synthesized by the condensation of 2,2 0 -dihydroxybiphenyl [BPh] and thiourea [Th] with formaldehyde [F] in the presence of acid catalyst and using varied molar ratios of reacting monomers. Terpolymer resin compositions have been determined on the basis of their elemental analysis, and the number average molecular weights of these resins were determined by conductometric titration in nonaqueous medium. Viscometric measurements in dimethyl formamide (DMF) have been carried out with a view to ascertain the characteristic functions and constants. UV-vis, FTIR, and NMR spectra were studied to elucidate the structure.

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Disposition Kinetic of Levofloxacin in Experimentally Induced Febrile Model of Sheep

Cited by 45 publications

References 24 publications

Dyeing of Textiles with Natural Dyes

Dyeing of Textiles with Natural Dyes

Synthesis and characterizations of novel thiazolyl-thiadiazole derivatives as telomerase activators

Resins IV: Preparation and characterization of terpolymer resins prepared from biphenol, thiourea and formaldehyde

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