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Relevant bibliographies by topics / Phenylthiourea

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Academic literature on the topic 'Phenylthiourea'

Author: Grafiati

Published: 4 June 2021

Last updated: 27 July 2025

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Journal articles on the topic "Phenylthiourea"

1

Kaválek, Jaromír, Josef Jirman, and Vojeslav Štěrba. "Kinetics and mechanism of rearrangement and methanolysis of acylphenylthioureas." Collection of Czechoslovak Chemical Communications 50, no. 3 (1985): 766–78. http://dx.doi.org/10.1135/cccc19850766.

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S-Acyl-1-phenylthioureas and their 3-methyl derivatives are rearranged to 1-acyl derivatives of thiourea in methanolic solution. The rearrangement of the 1-acyl-1-phenyl derivative to the thermodynamically more stable 3-acyl derivative is subject to specific base catalysis. The rearrangement of acetyl group is about 2 orders of magnitude slower than that of benzoyl group. 1-Acetyl-l-phenylthiourea undergoes base-catalyzed methanolysis (giving phenylthiourea and methyl acetate) instead of the rearrangement. The methanolysis rates of l-acyl-3-phenylthioureas and their N-methyl derivatives have b

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2

Shen, Yi-Hong, and Duan-Jun Xu. "Phenylthiourea." Acta Crystallographica Section E Structure Reports Online 60, no. 7 (2004): o1193—o1194. http://dx.doi.org/10.1107/s1600536804013947.

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3

D. Kesuma, Siswandono, and A. Kirtishanti. "MOLECULAR DOCKING AND BIOLOGICAL ACTIVITY OF N- (4-METHOXY)-BENZOYL-N’-PHENYLTHIOUREA AND N-(4- TRIFLUORO)-BENZOYL-N’-PHENYLTHIOUREA AS ANTIBREAST CANCER CANDIDATES." RASAYAN Journal of Chemistry 15, no. 02 (2022): 1503–8. http://dx.doi.org/10.31788/rjc.2022.1526836.

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Current breast cancer therapy does not always work optimally, and cases of resistance have been reported. Therefore, it is imperative to develop new effective drugs with minimal side effects through predictions of the epidermal growth factor receptor (EGFR) signalling pathway inhibition. Among chemicals with the potential as anticancer candidates for breast cancer are phenylthiourea derivatives. In this study, two phenylthiourea derivatives were synthesized: N- (4-methoxy)-benzoyl-N'-phenylthiourea and N-(4-trifluoromethyl)-benzoyl-N'-phenylthiourea. These compounds were docked with the EGFR r

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4

B., H. Zaware, A. Mane R., and B. Ingle D. "Kinetics of reaction of chloroacetone with thioureas." Journal of Indian Chemical Society Vol. 77, Apr 2000 (2000): 213–14. https://doi.org/10.5281/zenodo.5867060.

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Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University, Aurangabad-431 004, India <em>Manuscript received 20 July 1998, revised 16 August 1999, accepted 26 November 1999</em> The second order rate constants for the reactions of chloroacetone with thiourea, phenylthiourea and p-substituted phenylthioureas have been evaluated in ethanol medium. The rate of reaction is first order with respect to chloroacetone and first order with respect to thioureas. The effect of substituents on the rate of reaction is also studied. Thermodynamic parameters are used to explain the nature of reac

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5

Kesuma, Dini, Aguslina Kirtishanti, Citra H. A. Makayasa, and I. Gede A. Sumartha. "Anticancer activity of N-(4-t-butylbenzoyl)-N’-phenylthiourea: Molecular docking, synthesis, and cytotoxic activity in breast and cervical cancer cells." Journal of Pharmacy & Pharmacognosy Research 11, no. 2 (2023): 208–15. http://dx.doi.org/10.56499/jppres22.1508_11.2.208.

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Context: N-(4-t-butylbenzoyl)-N’-phenylthiourea, a derivative compound of N-benzoyl-N’-phenylthiourea, has relatively high lipophilicity with the epidermal growth factor receptor and silent mating type information regulation-1 enzyme as its molecular targets. Aims: To determine the anticancer activity of N-(4-t-butylbenzoyl)-N’-phenylthiourea as an in silico and in vitro anticancer candidate for the breast and cervical cancer. Methods: In silico test was performed to predict the cytotoxic activity using AutoDock Vina. This activity was also measured in vitro using the Microculture Tetrazolium

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6

Yusof, M. Sukeri M., Siti 'Afifah Tunnur M. Asrab, and Bohari M. Yamin. "N-Cyclohexylcarbonyl-N′-phenylthiourea." Acta Crystallographica Section E Structure Reports Online 63, no. 12 (2007): o4627. http://dx.doi.org/10.1107/s1600536807055079.

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7

Yamin, Bohari M., and M. Sukeri M. Yusof. "N-Benzoyl-N′-phenylthiourea." Acta Crystallographica Section E Structure Reports Online 59, no. 2 (2003): o151—o152. http://dx.doi.org/10.1107/s1600536802023711.

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8

Zhang, You-Ming, Tai-Bao Wei, Liang Xian, Qi Lin, and Kai-Bei Yu. "N-Ethoxycarbonyl-N′-phenylthiourea." Acta Crystallographica Section E Structure Reports Online 59, no. 7 (2003): o905—o906. http://dx.doi.org/10.1107/s1600536803011607.

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9

Su, Hou-xiang. "1-Methyl-3-phenylthiourea." Acta Crystallographica Section E Structure Reports Online 70, no. 5 (2014): o528. http://dx.doi.org/10.1107/s1600536814007442.

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The title compound, C8H10N2S, was prepared by reaction of methylamine solution, KOH and phenyl-isothiocyanate in ethanol. It adopts asyn-Me andanti-Ph conformation relative to the C=S double bond. The dihedral angle between the N—C(=S)—N thiourea and phenyl planes is 67.83 (6)°. In the crystal, the molecules centrosymmetrical dimers by pairs of N(Ph)—H...S hydrogen bonds. The dimers are linked by N(Me)—H...S hydrogen bonds into layers parallel to (100).

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10

Ramnathan, A., K. Sivakumar, K. Subramanian, N. Srinivasan, K. Ramadas, and H. K. Fun. "1-Cyclohexyl-3-phenylthiourea." Acta Crystallographica Section C Crystal Structure Communications 52, no. 3 (1996): 656–58. http://dx.doi.org/10.1107/s0108270195014065.

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Books on the topic "Phenylthiourea"

1

Prescott, John, and Beverly J. Tepper. Genetic Variation in Taste Sensitivity. Taylor & Francis Group, 2004.

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Prescott, John, and Beverly J. Tepper. Genetic Variation in Taste Sensitivity. Taylor & Francis Group, 2004.

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Genetic Variation in Taste Sensitivity (Food Science and Technology). CRC, 2004.

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Prescott, John, and Beverly J. Tepper. Genetic Variation in Taste Sensitivity. Taylor & Francis Group, 2004.

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Prescott, John, and Beverly J. Tepper. Genetic Variation in Taste Sensitivity. Taylor & Francis Group, 2004.

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Prescott, John, and Beverly J. Tepper. Genetic Variation in Taste Sensitivity. Taylor & Francis Group, 2004.

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Prescott, John, and Beverly J. Tepper. Genetic Variation in Taste Sensitivity. Taylor & Francis Group, 2004.

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Book chapters on the topic "Phenylthiourea"

1

"Phenylthiourea." In Encyclopedia of Genetics, Genomics, Proteomics and Informatics. Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-6754-9_12707.

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2

KAMMÜLLER, M. E., A. H. PENNINKS, and W. SEINEN. "Cyclization Products of Phenylthiourea Compounds in Adulterated Rapeseed Oil as possible Aetiological Factor in Spanish Toxic Oil Syndrome." In Advances in Immunopharmacology. Elsevier, 1986. http://dx.doi.org/10.1016/b978-0-08-032008-3.50062-x.

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3

Ramasamy Sivakumar, Mullaivanam, and Rangasamy Shanthi. "Plasma and Hemocyanin Phenoloxidase Derived from the Hemolymph of Giant Freshwater Prawn Macrobrachium rosenbergii (De Man, 1879)." In Crustacea - Nano, Micro and Macro Studies [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.104268.

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We attempted to study the immune response in M. rosenbergii by melanization reaction produced by plasma phenoloxidase (PO) activity. The substrate affinity of the PO enzyme was determined using different phenolic substrates, and it was found that the diphenols were only oxidized. The enzyme was characterized as catechol oxidase type of PO and L-3,4 dihydroxyphenylalanine (L-DOPA) showed the highest substrate affinity to the enzyme. The biochemical parameters that determined optimum enzyme activity were found to be 2.5 mM L-DOPA at an absorbance of 470 nm, 10 mM Tris–HCl buffer at pH 7.5, tempe

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Conference papers on the topic "Phenylthiourea"

1

Trabanelli, G., A. Frignani, G. Brunoro, C. Monticelli, and F. Zucchi. "Corrosion and Inhibition of Low Alloyed Chromium Steels in Hydrofluoric Acid Solutions." In CORROSION 1985. NACE International, 1985. https://doi.org/10.5006/c1985-85376.

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Abstract This paper investigates the influence chromium content exerts on the corrosion resistance of low alloyed chromium steels in hydrofluoric acid solution and compares it with the corrosion resistance in other acids, such as hydrochloric, perchloric and sulphuric. Weight losses were performed on ASTM A 106 steel and on ASTM A335 type steel (chromium content: 1.5-10%) in 1.7 N HF; 1.4 N HCl; 1.5 N H2SO4 and 1.5 N HClO4 at 45 °C. These tests showed that chromium decreases the corrosion resistance of the tested iron-chromium alloys in HClO4, H2SO4 and especially in HF solutions. Different pu

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2

Zhang, Di, Zhilong Ding, Tiantian Guo, et al. "Experimental and theoretical studies on THz spectra of phenylthiourea compounds." In 2013 38th International Conference on Infrared, Millimeter, and Terahertz Waves (IRMMW-THz 2013). IEEE, 2013. http://dx.doi.org/10.1109/irmmw-thz.2013.6665547.

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3

Zevallos-Delgado, Christian, Taye Mekonnen, Yogeshwari S. Ambekar, et al. "Assessment of the biomechanical changes on zebrafish larvae eye development caused by phenylthiourea (PTU) treatment using reverberant optical coherence elastography (Rev-OCE)." In Optical Elastography and Tissue Biomechanics XI, edited by Kirill V. Larin and Giuliano Scarcelli. SPIE, 2024. http://dx.doi.org/10.1117/12.3003390.

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4

Khan, Adnan, Amani Hassanein, Abdul Shakoor, Ramazan kahraman, Fatima Montemor, and Anwarul Hasan. "Hybrid Microcapsules Reinforced Smart Coatings for Corrosion Protection in Oil and Gas Industry." In Qatar University Annual Research Forum & Exhibition. Qatar University Press, 2020. http://dx.doi.org/10.29117/quarfe.2020.0014.

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Corrosion is one of the critical causes of material loss in metal components. This research is focused on the synthesis, and electrochemical properties of polyelectrolyte layered microcapsules (PMCs) reinforced smart polymeric coating for corrosion protection of steel substrates. For this purpose, monolayer urea-formaldehyde microcapsules encapsulated with linalyl acetate (MLMCs) was synthesized by Insitu polymerization. In the next step, phenylthiourea (PTU) was loaded between the layers of polyelectrolytes; polyethylenimine (PEI) & sulfonated polyether ether ketone (SPEEK) on the surface

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