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Journal articles on the topic 'Dabsyl'

Author: Grafiati

Published: 4 June 2021

Last updated: 2 February 2022

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1

Lin, Jen-Kun, Su-Chen Chang, and Chian-Chyi Huang. "HPLC Determination of Amino And Carbonyl Compounds with Dabsyl Chloride and Dabsyl Hydrazine." Journal of the Chinese Chemical Society 36, no. 4 (1989): 279–92. http://dx.doi.org/10.1002/jccs.198900041.

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2

Alpertunga, Buket, Sidika Sungur, Lale Ersoy та Sabiha Yalçin Manav. "Determination of Some β-Blockers as Dabsyl Derivatives by HPLC". Archiv der Pharmazie 323, № 9 (1990): 587–89. http://dx.doi.org/10.1002/ardp.19903230906.

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3

Watanabe, Daisuke, Yuko Kazui, and Hikoto Ohta. "A rapid screening color test for glyphosate using dabsyl derivatization." Forensic Toxicology 37, no. 2 (2018): 443–48. http://dx.doi.org/10.1007/s11419-018-00460-z.

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4

Satoh, Hiroyasu, Takashi Mino, and Tomonori Matsuo. "Anaerobic uptake of glutamate and aspartate by enhanced biological phosphorus removal activated sludge." Water Science and Technology 37, no. 4-5 (1998): 579–82. http://dx.doi.org/10.2166/wst.1998.0721.

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Mechanisms of the anaerobic uptake of glutamate and aspartate by enhanced biological phosphorus removal activated sludge were investigated. Sludge hydrolysate with hydrochloric acid was analyzed by reverse phase HPLC after pre column derivatization with dabsyl-chloride. The experimental results indicated that glutamate is accumulated as a polymer consisting of γ-aminobutyric acid and an unknown amino acid. On the other hand, aspartate was found to be deaminated and then accumulated as PHA.

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5

Alpdogan, Güzin, and Sidika SUNGUR. "Determination of Homocystine as Dabsyl Derivative by Hplc Using Precolumn Derivatization." Analytical Letters 33, no. 13 (2000): 2645–51. http://dx.doi.org/10.1080/00032710008543213.

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6

Bockhardt, Annette, Ingolf Krause, and Henning Klostermeyer. "Determination of biogenic amines by RP-HPLC of the dabsyl derivates." Zeitschrift f�r Lebensmittel-Untersuchung und -Forschung 203, no. 1 (1996): 65–70. http://dx.doi.org/10.1007/bf01267772.

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7

Hameau, Aurélien, Sabine Fuchs, Régis Laurent, Jean-Pierre Majoral, and Anne-Marie Caminade. "Synthesis of dye/fluorescent functionalized dendrons based on cyclotriphosphazene." Beilstein Journal of Organic Chemistry 7 (November 28, 2011): 1577–83. http://dx.doi.org/10.3762/bjoc.7.186.

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Functionalized phenols based on tyramine were synthesized in order to be selectively grafted on to hexachlorocyclotriphosphazene, affording a variety of functionalized dendrons of type AB5. The B functions comprised fluorescent groups (dansyl) or dyes (dabsyl), whereas the A function was provided by either an aldehyde or an amine. The characterization of these dendrons is reported. An unexpected behaviour of a fluorescent and water-soluble dendron based on dansyl groups in mixtures of dioxane/water was observed.

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8

SATO, Eisuke, Hiromi HATTORI, and Yuichi KANAOKA. "Fluorogenic Bimane Substrates with Dabsyl Group for Endopeptidases; Chymotrypsin, Collagenase and Thermolysin." Journal of Pharmacobio-Dynamics 14, no. 10 (1991): 599–604. http://dx.doi.org/10.1248/bpb1978.14.599.

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9

Dewitte, P. A., J. F. Cuveele, W. J. Merlevede, and J. R. Vandenheede. "Analysis of Phosphorylhydroxyamino Acids Present in Hydrolyzed Cell Extracts Using Dabsyl Derivatization." Analytical Biochemistry 226, no. 1 (1995): 1–9. http://dx.doi.org/10.1006/abio.1995.1183.

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10

Gorbics, Livia, Laszlo Urge, and Laszlo Otvos. "Comparative and optimized dabsyl-amino acid analysis of synthetic phosphopeptides and glycopeptides." Journal of Chromatography A 676, no. 1 (1994): 169–76. http://dx.doi.org/10.1016/0021-9673(94)80459-1.

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11

Heber, M., Chr Liedtke, H. Korte, et al. "Non-radioactive determination of PTH and dabsyl phosphoamino acids by capillary electrophoresis." Chromatographia 33, no. 7-8 (1992): 347–50. http://dx.doi.org/10.1007/bf02275916.

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12

Sethuraman, Rama, Malathi G. Krishnamoorthy, Tat-Leang Lee, et al. "Simultaneous Analysis of d- and l-Serine in Cerebrospinal Fluid by Use of HPLC." Clinical Chemistry 53, no. 8 (2007): 1489–94. http://dx.doi.org/10.1373/clinchem.2007.086702.

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Abstract Background: d-Serine is a coagonist for the glycine-binding site of the N-methyl-d-aspartate receptors and has been implicated in various neuropsychiatric functions such as learning, memory, and nociception, as well as schizophrenia and Alzheimer disease. We developed an HPLC method for d- and l-serine in cerebrospinal fluid (CSF). Methods: The dabsylated racemic serine peak, automatically collected using a previously reported HPLC separation process for CSF amino acids, was desalted and subjected to a chiral resolution HPLC step with a Sumichiral column using an ultraviolet-visible d

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13

Sato, Yasuyo, Masao Bounoshita, Keijin Iwaya, Toshihiko Miyaji, and Muneo Saito. "High-Speed Separation of Dabsyl-Amino Acids by Ultra High-Performance Liquid Chromatography." BUNSEKI KAGAKU 59, no. 9 (2010): 823–28. http://dx.doi.org/10.2116/bunsekikagaku.59.823.

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14

Jansen, Eugène H. J. M., Rijk H. van den Berg, Reinskje Both-Miedema, and Lambert Doorn. "Advantages and limitations of pre-column derivatization of amino acids with dabsyl chloride." Journal of Chromatography A 553 (August 1991): 123–33. http://dx.doi.org/10.1016/s0021-9673(01)88480-6.

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15

Hughes, Graham J., Séverine Frutiger, and Christian Fonck. "Quantitative high-performance liquid chromatographic analysis of dabsyl-amino acids within 14 min." Journal of Chromatography A 389 (January 1987): 327–33. http://dx.doi.org/10.1016/s0021-9673(01)94443-7.

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16

Hayashida, Osamu, and Yu Kaku. "Synthesis of Dabsyl-Appended Cyclophanes and Their Heterodimer Formation with Pyrene-Appended Cyclophanes." Journal of Organic Chemistry 78, no. 20 (2013): 10437–42. http://dx.doi.org/10.1021/jo4018843.

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17

Drnevich, Daryl, and Thomas C. Vary. "Analysis of physiological amino acids using dabsyl derivatization and reversed-phase liquid chromatography." Journal of Chromatography B: Biomedical Sciences and Applications 613, no. 1 (1993): 137–44. http://dx.doi.org/10.1016/0378-4347(93)80207-k.

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18

MURAMOTO, Koji, and Hisao KAMIYA. "Analyses of dansyl and dabsyl amino acids by reverse-phase high-performance liquid chromatography." NIPPON SUISAN GAKKAISHI 51, no. 5 (1985): 817–24. http://dx.doi.org/10.2331/suisan.51.817.

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19

Vendrell, Josep, and Francesc X. Avilés. "Complete amino acid analysis of proteins by dabsyl derivatization and reversed-phase liquid chromatogrphy." Journal of Chromatography A 358 (January 1986): 401–13. http://dx.doi.org/10.1016/s0021-9673(01)90354-1.

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20

Ikeda, M., K. Sorimachi, K. Akimoto, M. Okazaki, M. Sunagawa, and A. Niwa. "Analysis of hydroxyproline in urine by high-performance liquid chromatography after dabsyl-chloride derivatization." Amino Acids 8, no. 4 (1995): 401–7. http://dx.doi.org/10.1007/bf00806559.

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21

Witek, A., H. Hopkala, and G. Matysik. "TLC-densitometric determination of bisoprolol, labetalol and propafenone, as dabsyl derivatives, in pharmaceutical preparations." Chromatographia 50, no. 1-2 (1999): 41–44. http://dx.doi.org/10.1007/bf02493615.

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22

Koski, Pertti, Ilkka M. Helander, Matti Sarvas, and Martti Vaara. "Analysis of polyamines as their dabsyl derivatives by reversed-phase high-performance liquid chromatography." Analytical Biochemistry 164, no. 1 (1987): 261–66. http://dx.doi.org/10.1016/0003-2697(87)90395-2.

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23

Turpeinen, U., and U. M. Pomoell. "Liquid chromatography of free hydroxyproline in serum." Clinical Chemistry 31, no. 10 (1985): 1710–12. http://dx.doi.org/10.1093/clinchem/31.10.1710.

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Abstract We report a "high-performance" liquid-chromatographic method for measuring free hydroxyproline in serum. After separating the free hydroxyproline from the protein- and peptide-bound forms by centrifugal ultrafiltration, we derivatize the free form with 4-dimethylaminoazobenzene-4'-sulfonyl ("dabsyl") chloride and separate and quantify the derivative on a C18 chromatographic column. The mobile phase is sodium acetate buffer and acetonitrile, in a multilinear solvent gradient. The derivative is detected at 436 nm. Mean analytical recovery was 73%. The assay curve is linear from 14 to 21

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24

Chen, Yi-Hong, Ya-Ping Lin, Su-Er Liou, and Chu-Chin Chen. "Mass spectrometric determination of dabsyl-chloride derivatised anserine, carnosine and taurine in commercial chicken essences." International Journal of Food Science & Technology 42, no. 5 (2007): 593–600. http://dx.doi.org/10.1111/j.1365-2621.2006.01282.x.

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25

Faraji, Mohammad, and Parisa Amini Kadijani. "Dabsyl chloride derivatisation of melamine followed by high-performance liquid chromatography determination in water samples." International Journal of Environmental Analytical Chemistry 96, no. 15 (2016): 1430–39. http://dx.doi.org/10.1080/03067319.2016.1267160.

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26

CHEN, Yi-Hong, Ling-Ling SHIH, Su-Er LIOU, and Chu-Chin CHEN. "Analysis of Dabsyl-Cl Derivated Amino Acids by High Performance Liquid Chromatography and Tandem Mass Spectrometry." Food Science and Technology Research 9, no. 3 (2003): 276–82. http://dx.doi.org/10.3136/fstr.9.276.

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27

Siiman, O., R. Smith, C. Blatchford, and M. Kerker. "Combined surface-enhanced and surface resonance Raman spectra of dabsyl aspartate adsorbed on a silver electrode." Langmuir 1, no. 1 (1985): 90–96. http://dx.doi.org/10.1021/la00061a014.

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28

Lepp, Adam, and Olavi Siiman. "Surface raman investigation of the sorption of dabsyl aspartate and polyvinylpyrrolidone on colloidal silver in ethanol." Journal of Colloid and Interface Science 105, no. 2 (1985): 325–41. http://dx.doi.org/10.1016/0021-9797(85)90306-6.

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29

Zaramella, Alessio, Nadia Conti, Michele Dal Cin, Alfredo Paio, Pierfausto Seneci, and Sylvie Gehanne. "Dansyl and Dabsyl Analytical Constructs as Tools for the Accurate Estimation of Compounds in Solid-Phase Synthesis." Journal of Combinatorial Chemistry 3, no. 5 (2001): 410–20. http://dx.doi.org/10.1021/cc0001147.

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30

Lacroix, C., and E. Saussereau. "Fast liquid chromatography/tandem mass spectrometry determination of cannabinoids in micro volume blood samples after dabsyl derivatization." Journal of Chromatography B 905 (September 2012): 85–95. http://dx.doi.org/10.1016/j.jchromb.2012.08.006.

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31

Castillo, M. A., and R. C. Castells. "Procedure for the determination of biogenic amines by derivatization with dabsyl chloride and reversed phase liquid chromatography." Chromatographia 54, no. 11-12 (2001): 711–16. http://dx.doi.org/10.1007/bf02492488.

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32

Lepp, Adam, and Olavi Siiman. "Surface resonance Raman and surface-enhanced Raman scattering excitation profiles for dabsyl aspartate on colloidal silver in ethanol." Journal of Physical Chemistry 89, no. 16 (1985): 3494–502. http://dx.doi.org/10.1021/j100262a015.

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33

Siiman, Olavi, and Wan Peter Hsu. "Surface-enhanced Raman scattering (SERS) enhancements and excitation profiles for 3,5-pyridinedicarboxylate and dabsyl aspartate on colloidal gold." Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases 82, no. 3 (1986): 851. http://dx.doi.org/10.1039/f19868200851.

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34

Romero, R., M. G. Bagur, M. Sánchez-Viñas, and D. Gázquez. "Optimization of experimental variables in the dabsyl chloride derivatization of biogenic amines for their determination by RP-HPLC." Chromatographia 51, no. 7-8 (2000): 404–10. http://dx.doi.org/10.1007/bf02490476.

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35

Ikeda, Masashi, Kenji Sorimachi, Kazumi Akimoto, and Yosihiro Yasumura. "Reversed-phase high-performance liquid chromatographic analysis of hydroxyproline and proline from collagen by derivatization with dabsyl chloride." Journal of Chromatography B: Biomedical Sciences and Applications 621, no. 2 (1993): 133–38. http://dx.doi.org/10.1016/0378-4347(93)80088-l.

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36

Tintoré, Maria, Anna Aviñó, Federico M. Ruiz, Ramón Eritja, and Carme Fàbrega. "Development of a Novel Fluorescence Assay Based on the Use of the Thrombin-Binding Aptamer for the Detection ofO6-Alkylguanine-DNA Alkyltransferase Activity." Journal of Nucleic Acids 2010 (2010): 1–9. http://dx.doi.org/10.4061/2010/632041.

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HumanO6-alkylguanine-DNA alkyltransferase (hAGT) is a DNA repair protein that reverses the effects of alkylating agents by removing DNA adducts from theO6position of guanine. Here, we developed a real-time fluorescence hAGT activity assay that is based on the detection of conformational changes of the thrombin-binding aptamer (TBA). The quadruplex structure of TBA is disrupted when a central guanine is replaced by anO6-methyl-guanine. The sequence also contains a fluorophore (fluorescein) and a quencher (dabsyl) attached to the opposite ends. In the unfolded structure, the fluorophore and the

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37

Krause, Ingolf, Annette Bockhardt, Herbert Neckermann, Thomas Henle, and Henning Klostermeyer. "Simultaneous determination of amino acids and biogenic amines by reversed-phase high-performance liquid chromatography of the dabsyl derivatives." Journal of Chromatography A 715, no. 1 (1995): 67–79. http://dx.doi.org/10.1016/0021-9673(95)00578-b.

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38

Yu, Margaret, and Norman J. Dovichi. "Sub-femtomole determination of DABSYL-amino acids with capillary zone electrophoresis separation and laser-induced thermo-optical absorbance detection." Mikrochimica Acta 96, no. 1-6 (1988): 27–40. http://dx.doi.org/10.1007/bf01236090.

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39

Zhao, Hui, Hao Fan, Jinxiang Ceng, Qianggen Li, Yan Lin, and Xiaoyun Wang. "A New Electrochemical Biosensor of Host-guest Recognition Mode for DNA Hybridization Detection." Journal of New Materials for Electrochemical Systems 15, no. 1 (2011): 11–14. http://dx.doi.org/10.14447/jnmes.v15i1.82.

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This paper reports on an electrochemical biosensor to detect the hybridization specificity by using host-guest recognition technique. A hairpin DNA with a dabcyl molecule which is typical guest molecule to b-Cyclodextrins (b-CD) at the 3’-terminus and a NH2 linked at the 5’-terminus as the probe DNA. The probe DNA was immobilized on the PdS nanoparticle to construct a double-labeled probe (DLP) and could selectively hybridize with its target DNA. A b-CD modified Poly(N-acetylaniline) glassy carbon electrode was used for capturing dabcyl in DLP. Without binding with target DNA, the DLP keep ste

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40

Soares, Maria Elisa, F�lix Carvalho, and Maria de Lourdes Bastos. "Determination of amphetamine and its metabolitep-hydroxyamphetamine in rat urine by reversed-phase high-performance liquid chromatography after dabsyl derivatization." Biomedical Chromatography 15, no. 7 (2001): 452–56. http://dx.doi.org/10.1002/bmc.93.

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41

Romero, Roberto, Jan Åke Jönsson, Domingo Gázquez, M. Gracia Bagur, and Mercedes Sánchez-Viñas. "Multivariate optimization of supported liquid membrane extraction of biogenic amines from wine samples prior to liquid chromatography determination as dabsyl derivatives." Journal of Separation Science 25, no. 9 (2002): 584–92. http://dx.doi.org/10.1002/1615-9314(20020601)25:9<584::aid-jssc584>3.0.co;2-f.

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42

PINHO, OLIVIA, ANA I. E. PINTADO, ANA M. P. GOMES, M. MANUELA E. PINTADO, F. XAVIER MALCATA, and ISABEL M. P. L. V. O. FERREIRA. "Interrelationships among Microbiological, Physicochemical, and Biochemical Properties of Terrincho Cheese, with Emphasis on Biogenic Amines." Journal of Food Protection 67, no. 12 (2004): 2779–85. http://dx.doi.org/10.4315/0362-028x-67.12.2779.

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Changes in the microbiological, physicochemical, and biochemical characteristics of Terrincho cheese as represented by native microflora, pH, water activity, soluble nitrogen fractions, free amino acids, and biogenic amines (e.g., ethylamine, dimethylamine, tryptamine, phenylethylamine, putrescine, cadaverine, histamine, tyramine, cystamine, and spermine) during ripening were monitored. Terrincho is a traditional Portuguese cheese manufactured from raw ewe's milk. The main groups of microorganisms (lactococci, lactobacilli, enterococci, pseudomonads, staphylococci, coliforms, yeasts, and molds

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43

Li, Fuqiang, Hongchen Wang, and Jinxin He. "Synthesis and application of an alkaline crosslinking agent containing acrylamide as the durable press finishing agent on cotton fabric." Textile Research Journal 89, no. 11 (2018): 2084–97. http://dx.doi.org/10.1177/0040517518786271.

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In this study, acrylamide-containing crosslinking agents 2,4-diacrylamidebenzenesulfonic acid (AC-DABS1) and 2,5-diacrylamidebenzenesulfonic acid (AC-DABS2) were synthesized and applied to cotton fabric as durable press finishing agents under alkaline conditions. The target products were characterized by high-performance liquid chromatography (HPLC) and proton nuclear magnetic resonance. The stability of the acrylamide group in alkaline solution was investigated by model compound para-acrylamidebenzenesulfonic acid. The efficiency of AC-DABS1 and AC-DABS2 as durable press finishing agents was

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44

De Mey, E., G. Drabik-Markiewicz, H. De Maere, et al. "Dabsyl derivatisation as an alternative for dansylation in the detection of biogenic amines in fermented meat products by reversed phase high performance liquid chromatography." Food Chemistry 130, no. 4 (2012): 1017–23. http://dx.doi.org/10.1016/j.foodchem.2011.07.124.

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45

Zarghampour, Fereshteh, Yadollah Yamini, Mahroo Baharfar, and Mohammad Faraji. "Electromembrane extraction of biogenic amines in food samples by a microfluidic-chip system followed by dabsyl derivatization prior to high performance liquid chromatography analysis." Journal of Chromatography A 1556 (June 2018): 21–28. http://dx.doi.org/10.1016/j.chroma.2018.04.046.

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46

Handley, Michael K., Walter W. Hirth, James G. Phillips, et al. "Development of a sensitive and quantitative analytical method for 1H-4-substituted imidazole histamine H3-receptor antagonists utilizing high-performance liquid chromatography and dabsyl derivatization." Journal of Chromatography B: Biomedical Sciences and Applications 716, no. 1-2 (1998): 239–49. http://dx.doi.org/10.1016/s0378-4347(98)00272-2.

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47

Cifuentes, Cristina, Sigrid Mennickent, and Marta De Diego. "Quantitative Determination of Topiramate in Human Serum and Umbilical Cord Blood." Current Pharmaceutical Analysis 15, no. 5 (2019): 521–27. http://dx.doi.org/10.2174/1573412914666180502124419.

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Background: Topiramate (TPM), an anticonvulsant drug, was determined in human serum and in umbilical cord blood. TPM can produce severe damage to the fetus (baby into mother´s uterus), and it is not always possible that epileptic women change their drug during pregnancy, because some antiepileptic drugs are not effective on some people. Using pregnant-mother serum blood, we can estimate drug levels in fetus serum, and by umbilical cord blood, is possible estimate drug levels in serum babies, without the ethic aspects to withdrawal blood of them. Methods: Quantitation was achieved by LC/DAD, us

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48

Krzek, Jan, Joanna Piotrowska, Barbara Żuromska-Witek, Urszula Hubicka, and Ewelina Łysoń. "Validation of the method of identification and quantitative determination of bacitracin in the form of bacitracin derivative with dabsyl chloride by thin-layer chromatography and densitometry." Journal of Planar Chromatography – Modern TLC 26, no. 1 (2013): 67–72. http://dx.doi.org/10.1556/jpc.26.2013.1.10.

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49

Faraji, M., and M. Adeli. "Sensitive determination of melamine in milk and powdered infant formula samples by high-performance liquid chromatography using dabsyl chloride derivatization followed by dispersive liquid–liquid microextraction." Food Chemistry 221 (April 2017): 139–46. http://dx.doi.org/10.1016/j.foodchem.2016.10.002.

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50

GOMES, Ricardo, Marta SOUSA SILVA, Alexandre QUINTAS, et al. "Argpyrimidine, a methylglyoxal-derived advanced glycation end-product in familial amyloidotic polyneuropathy." Biochemical Journal 385, no. 2 (2005): 339–45. http://dx.doi.org/10.1042/bj20040833.

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FAP (familial amyloidotic polyneuropathy) is a systemic amyloid disease characterized by the formation of extracellular deposits of transthyretin. More than 80 single point mutations are associated with amyloidogenic behaviour and the onset of this fatal disease. It is believed that mutant forms of transthyretin lead to a decreased stability of the tetramer, which dissociates into monomers that are prone to unfolding and aggregation, later forming β-fibrils in amyloid deposits. This theory does not explain the formation of β-fibrils nor why they are toxic to nearby cells. Age at disease onset

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