Academic literature on the topic '-(4-aminophenyl) benzothiazoles'

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Journal articles on the topic "-(4-aminophenyl) benzothiazoles"

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Hutchinson, Ian, Mei-Sze Chua, Helen L. Browne, et al. "Antitumor Benzothiazoles. 14.1Synthesis and in Vitro Biological Properties of Fluorinated 2-(4-Aminophenyl)benzothiazoles." Journal of Medicinal Chemistry 44, no. 9 (2001): 1446–55. http://dx.doi.org/10.1021/jm001104n.

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Zhang, Yang, Mrinal Chakraborty, Christian G. Cerda-Smith, et al. "Chemistry of Ring-Substituted 4-(Benzothiazol-2-yl)phenylnitrenium Ions from Antitumor 2-(4-Aminophenyl)benzothiazoles." Journal of Organic Chemistry 78, no. 14 (2013): 6992–7000. http://dx.doi.org/10.1021/jo400826f.

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Wheelhouse, Richard T., Dong-Fang Shi, Derry E. V. Wilman, and Malcolm F. G. Stevens. "Antitumour benzothiazoles. Part 4. An NMR study of the sites of protonation of 2-(4-aminophenyl)benzothiazoles." Journal of the Chemical Society, Perkin Transactions 2, no. 7 (1996): 1271. http://dx.doi.org/10.1039/p29960001271.

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Hutchinson, Ian, Sharon A. Jennings, B. Rao Vishnuvajjala, Andrew D. Westwell, and Malcolm F. G. Stevens. "Antitumor Benzothiazoles. 16.1Synthesis and Pharmaceutical Properties of Antitumor 2-(4-Aminophenyl)benzothiazole Amino Acid Prodrugs." Journal of Medicinal Chemistry 45, no. 3 (2002): 744–47. http://dx.doi.org/10.1021/jm011025r.

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WHEELHOUSE, R. T., D. F. SHI, D. E. V. WILMAN, and M. F. G. STEVENS. "ChemInform Abstract: Antitumor Benzothiazoles. Part 4. An NMR Study of the Sites of Protonation of 2-(4-Aminophenyl)benzothiazoles." ChemInform 27, no. 40 (2010): no. http://dx.doi.org/10.1002/chin.199640119.

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Gineinah, Magdy. "6-, 7- AND 8-(5-ARY L-1-PHENYL-2-PYRAZOLIN-3-LY)IMIDAZO- AND PYRIMIDO[2,1-b]BENZOTHIAZOLES AS NOVEL ANTICONVULSANT AGENTS." Scientia Pharmaceutica 69, no. 1 (2001): 53–61. http://dx.doi.org/10.3797/scipharm.aut-01-06.

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Some new derivatives of 2-amino-5- and 6-(5-aryl-1-phenyl-2-pyrazolin-3-yl)benzothiazole were synthesized from the corresponding aminophenyl compounds by reaction with KSCN/Br2 to build up the benzothiazole ring. The aminophenyl derivatives of pyrazoline were prepared by cyclization with phenylhydrazine of the appropriate 1,3-diphenyl-2-propen-1-one derivatives obtained from arninoacetophenone and differently substituted aldehydes. However, the newly synthesized 2-aminobenzothiazole derivatives of pyrazoline were subjected to cyclization with ethyl brornopyruvate to afford the formation of 6-
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Hutchinson, Ian, Mei-Sze Chua, Helen L. Browne, et al. "ChemInform Abstract: Antitumor Benzothiazoles. Part 14. Synthesis and in vitro Biological Properties of Fluorinated 2-(4-Aminophenyl)benzothiazoles." ChemInform 32, no. 30 (2010): no. http://dx.doi.org/10.1002/chin.200130136.

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Shi, Dong-Fang, Tracey D. Bradshaw, Mei-Sze Chua, Andrew D. Westwell, and Malcolm F. G. Stevens. "Antitumour Benzothiazoles. Part 15: The Synthesis and Physico-Chemical Properties of 2-(4-Aminophenyl)benzothiazole Sulfamate Salt Derivatives." Bioorganic & Medicinal Chemistry Letters 11, no. 8 (2001): 1093–95. http://dx.doi.org/10.1016/s0960-894x(01)00142-1.

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Shi, Dong-Fang, Tracey D. Bradshaw, Samantha Wrigley, et al. "Antitumor Benzothiazoles. 3.1Synthesis of 2-(4-Aminophenyl)benzothiazoles and Evaluation of Their Activities against Breast Cancer Cell LinesinVitroandin Vivo." Journal of Medicinal Chemistry 39, no. 17 (1996): 3375–84. http://dx.doi.org/10.1021/jm9600959.

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Kashiyama, Eiji, Ian Hutchinson, Mei-Sze Chua, et al. "Antitumor Benzothiazoles. 8.1Synthesis, Metabolic Formation, and Biological Properties of theC- andN-Oxidation Products of Antitumor 2-(4-Aminophenyl)benzothiazoles∇." Journal of Medicinal Chemistry 42, no. 20 (1999): 4172–84. http://dx.doi.org/10.1021/jm990104o.

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Dissertations / Theses on the topic "-(4-aminophenyl) benzothiazoles"

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Chua, Mei-Sze. "Anti-tumour 2-(4-aminophenyl)benzothiazoles : structurally simple but exciting candidates for clinical trials." Thesis, University of Nottingham, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.324051.

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Wrigley, Samantha. "Investigations of the subtle and selective antitumour properties of 2-(4-aminophenyl)-benzothiazole and related compounds." Thesis, University of Nottingham, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.338529.

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Chen, Yin-Kai, and 陳胤愷. "2-(4-aminophenyl)benzothiazole derivatives as photodynamic therapy agents in melanoma cell lines." Thesis, 2012. http://ndltd.ncl.edu.tw/handle/85918933431777158328.

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碩士<br>高雄醫學大學<br>生物科技學系碩士班<br>100<br>This thesis is to explore the 2-(4-aminophenyl)benzothiazole derivatives as a photosensitizer used in photodynamic therapy on melanoma cell. These compounds have strong absorption at UVA region. In previous reports, similar structures have been studied, after UVA excitation they cause cell apoptosis, so we were interested to screen if such type of compounds with UVA would have similar properties, so that they may be applied as photosensitizers. In the previous study, we found that the compound or on irradiation with low-dose UVA alone with cells will not be
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Kuo, Hsuan-Yu, and 郭炫瑜. "Effects of photosensitizer 2-(4-aminophenyl)benzothiazole plus UVA on cell viability and apoptosis in keloid fibroblasts." Thesis, 2012. http://ndltd.ncl.edu.tw/handle/01114323523944515879.

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碩士<br>高雄醫學大學<br>醫學檢驗生物技術學研究所<br>100<br>Keloid is characterized by excessive scar formation and exuberant collagen synthesis as a result of abnormal wound healing and dermal fibroblastic cell proliferation. Up to date, keloid is still a challenge to clinical therapy because of its high recurrence. In addition, there is no single treatment modality has been proven widely effective. Photodynamic therapy (PDT) is used to treat non-melanoma skin cancer and the mechanisms for PDT are well documented. Traditional PDT employed a combination of 5-aminolevulinic acid (ALA) and red light. However, the ef
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Book chapters on the topic "-(4-aminophenyl) benzothiazoles"

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Chua, M. S., T. D. Bradshaw, and M. F. G. Stevens. "2-(4-Aminophenyl)benzothiazoles: Agents with Selective and Potent Antitumour Activity in vitro and in vivo." In Contributions to Oncology. S. Karger AG, 1999. http://dx.doi.org/10.1159/000425852.

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