Academic literature on the topic 'Dihydroxybenzaldehyde'

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Journal articles on the topic "Dihydroxybenzaldehyde"

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Liu, Haibo, Jiaqian Wang, Yonglin He, et al. "Investigation of the binding properties of 3,4-dihydroxybenzaldehyde from Salvia miltiorrhiza (Bunge) with human serum albumin via multi-spectroscopic and molecular docking techniques." BioResources 17, no. 2 (2022): 2680–95. http://dx.doi.org/10.15376/biores.17.2.2680-2695.

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To investigate the binding properties of 3,4-dihydroxybenzaldehyde with human serum albumin, as well as the structural changes of human serum albumin under a simulated physiological pH value (a pH of 7.4) and a high 3,4-dihydroxybenzaldehyde concentration, a series of techniques, i.e., fluorescence, synchronous fluorescence, ultraviolet-visible absorption, Fourier-transform infrared spectroscopy, and molecular docking simulation, were employed. Steady state fluorescence showed that 3,4-dihydroxybenzaldehyde quenched the intrinsic fluorescence of human serum albumin via a static mechanism. The
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Ng, Seik Weng. "2,3-Dihydroxybenzaldehyde." Acta Crystallographica Section E Structure Reports Online 61, no. 7 (2005): o2301—o2302. http://dx.doi.org/10.1107/s1600536805019719.

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Kretz, Tonia, Hans-Wolfram Lerner, and Michael Bolte. "2,5-Dihydroxybenzaldehyde." Acta Crystallographica Section E Structure Reports Online 63, no. 12 (2007): o4673. http://dx.doi.org/10.1107/s160053680705595x.

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Tan, Kong Wai, Yang Farina, Chew Hee Ng, Mohd Jamil Maah, and Seik Weng Ng. "3,4-Dihydroxybenzaldehyde thiosemicarbazone." Acta Crystallographica Section E Structure Reports Online 64, no. 6 (2008): o1073. http://dx.doi.org/10.1107/s160053680801386x.

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O'Connor, Kevin E., Bernard Witholt, and Wouter Duetz. "p-Hydroxyphenylacetic Acid Metabolism inPseudomonas putida F6." Journal of Bacteriology 183, no. 3 (2001): 928–33. http://dx.doi.org/10.1128/jb.183.3.928-933.2001.

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ABSTRACT Pseudomonas putida F6 was found to metabolizep-hydroxyphenylacetic acid through 3,4-dihydroxyphenylacetic acid, 3,4-dihydroxymandelic acid, and 3,4-dihydroxybenzaldehyde. Cell extracts of P. putida F6 catalyze the NAD(P)H-independent hydroxylation ofp-hydroxyphenylacetic acid to 3,4-dihydroxyphenylacetic acid which is further oxidized to 3,4-dihydroxymandelic acid. Oxidation and decarboxylation of the latter yields 3,4-dihydroxybenzaldehyde. A red-brown color accompanies all of the above enzyme activities and is probably due to the polymerization of quinone-like compounds. 3,4-Dihydro
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Liu, Dong Wang, Xiao Ji Wang, Shuang Ping Huang, Lin Jun Tang, Shi Peng Chen, and Jian Ting Zhang. "Design and Synthesis of (E)-2-Hydroxy-4-Alkoxyl Salicylaldoxime Copper Extractant." Advanced Materials Research 785-786 (September 2013): 109–12. http://dx.doi.org/10.4028/www.scientific.net/amr.785-786.109.

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Synthesis of the series of compounds, which could be put into extract copper , contained hydroformylation, etherification, oximation. Resorcinol as the starting material was transformed to 2,4-dihydroxybenzaldehyde, and then converted to 2,4-dihydroxybenzaldehyde, which oximated to (E)-2-hydroxy-4-alkoxybenzaldehyde oxime.
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Tan, Kong Wai, Chew Hee Ng, Mohd Jamil Maah, and Seik Weng Ng. "2,5-Dihydroxybenzaldehyde 4-methylthiosemicarbazone." Acta Crystallographica Section E Structure Reports Online 64, no. 7 (2008): o1344. http://dx.doi.org/10.1107/s1600536808018801.

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Tan, Kong Wai, Yang Farina, Chew Hee Ng, Mohd Jamil Maah, and Seik Weng Ng. "3,4-Dihydroxybenzaldehyde 4-phenylthiosemicarbazone." Acta Crystallographica Section E Structure Reports Online 64, no. 6 (2008): o1035. http://dx.doi.org/10.1107/s1600536808013287.

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Tan, Kong Wai, Chew Hee Ng, Mohd Jamil Maah, and Seik Weng Ng. "2,4-Dihydroxybenzaldehyde 4-ethylthiosemicarbazone." Acta Crystallographica Section E Structure Reports Online 64, no. 11 (2008): o2123. http://dx.doi.org/10.1107/s160053680803300x.

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Tan, Kong Wai, Chew Hee Ng, Mohd Jamil Maah, and Seik Weng Ng. "2,4-Dihydroxybenzaldehyde 4-methylthiosemicarbazone." Acta Crystallographica Section E Structure Reports Online 64, no. 11 (2008): o2224. http://dx.doi.org/10.1107/s1600536808033308.

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Book chapters on the topic "Dihydroxybenzaldehyde"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex of Schiff base derived from 8-aminoquinoline and 2, 4-dihydroxybenzaldehyde." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_230.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex of Schiff base derived from 8-aminoquinoline and 2, 3-dihydroxybenzaldehyde." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_231.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of iron(III) complex of tridimensional Schiff-base ligand derived from 2, 3-dihydroxybenzaldehyde and tris(2-aminoethyl) amine." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-45972-0_400.

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M. Radanović, Mirjana, and Berta Barta Holló. "Some Aromatic Schiff Bases and Their Metal Complexes." In Schiff Base in Organic, Inorganic and Physical Chemistry [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.107405.

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Schiff bases represent a widely studied group of compounds, interesting from the synthetic and structural, but also applicational point of view. Among these, aromatic Schiff bases stand out due to their stability and possible application as safer therapeutic agents. Since the presence of the phenolic group and the heteroatom in the benzene ring seems to be of interest for the biological activity of Schiff bases, imine derivatives of some dihydroxybenzaldehydes, 2-acetylpyridine, and 2,6-diacetylpyridine are chosen to be described here. The syntheses, structural features, as well as investigati
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Conference papers on the topic "Dihydroxybenzaldehyde"

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Hussien, Nasry Jassim, Yang Farina, and Mohamad Jaber Al-Jeboori. "Synthesis and characterisation of diorganotin(IV) complexes of 3,4-dihydroxybenzaldehyde semicarbazone." In THE 2016 UKM FST POSTGRADUATE COLLOQUIUM: Proceedings of the Universiti Kebangsaan Malaysia, Faculty of Science and Technology 2016 Postgraduate Colloquium. Author(s), 2016. http://dx.doi.org/10.1063/1.4966744.

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