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Journal articles on the topic '2-(4-aminophenyl) benzothiazoles'

Author: Grafiati

Published: 5 June 2025

Last updated: 2 August 2025

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1

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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2

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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3

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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4

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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5

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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6

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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7

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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8

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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9

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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10

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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11

Hilal, Rifaat, Ahmed A. Abdel Khalek, and Shabaan A. K. Elroby. "DFT investigation of nitrenium ions derived from metabolism of antitumor 2-(4-aminophenyl)benzothiazoles." Journal of Molecular Structure: THEOCHEM 731, no. 1-3 (2005): 115–21. http://dx.doi.org/10.1016/j.theochem.2005.04.017.

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12

S, Priyanka. "Recent advances in Synthesis & Pharmacotherapeutic potential of Benzothiazoles." Der Pharma Chemica 14, no. 1 (2022): 2. https://doi.org/10.5281/zenodo.13353756.

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Isoquinoline is a heterocyclic aromatic organic compound. It is a structural isomer of quinoline. Isoquinoline and quinoline are benzopyridines, which are composed of a benzene ring fused to a pyridine ring. In a broader sense, the term isoquinoline is used to make reference to isoquinoline derivatives. 1-Benzylisoquinoline is the structural backbone in naturally occurring alkaloids including papaverine. The isoquinoline ring in these natural compounds derives from the aromatic amino acid tyrosine.

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13

Hutchinson, Ian, Tracey D. Bradshaw, Charles S. Matthews, Malcolm F. G. Stevens, and Andrew D. Westwell. "Antitumour benzothiazoles. Part 20: 3′-Cyano and 3′-Alkynyl-Substituted 2-(4′-Aminophenyl)benzothiazoles as new potent and selective analogues." Bioorganic & Medicinal Chemistry Letters 13, no. 3 (2003): 471–74. http://dx.doi.org/10.1016/s0960-894x(02)00930-7.

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14

Shi, Dong-Fang, Tracey D. Bradshaw, Mei-Sze Chua, Andrew D. Westwell, and Malcolm F. G. Stevens. "ChemInform Abstract: Antitumor Benzothiazoles. Part 15. The Synthesis and Physico-Chemical Properties of 2-(4-Aminophenyl)benzothiazole Sulfamate Salt Derivatives." ChemInform 32, no. 32 (2010): no. http://dx.doi.org/10.1002/chin.200132131.

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15

Lei, Yingjie, Xinshi Wu, Guochun Zhang, and Cuiling Ai. "Synthesis of 2-(4-aminophenyl)benzothiazoles using MF resin supported H+ under solvent free conditions." Russian Journal of General Chemistry 85, no. 3 (2015): 679–82. http://dx.doi.org/10.1134/s1070363215030251.

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16

Bradshaw, TD, S. Wrigley, D.-F. Shi, RJ Schultz, KD Paull, and MFG Stevens. "2-(4-Aminophenyl)benzothiazoles: novel agents with selective profiles of in vitro anti-tumour activity." British Journal of Cancer 77, no. 5 (1998): 745–52. http://dx.doi.org/10.1038/bjc.1998.122.

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17

Hilal, Rifaat, and Shabaan A. K. Elroby. "A QSAR study for 2-(4-aminophenyl)benzothiazoles: using DFT optimisation of geometry of molecules." Molecular Simulation 37, no. 1 (2011): 62–71. http://dx.doi.org/10.1080/08927022.2010.520133.

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18

Leong, C.-O., M. Gaskell, E. A. Martin, et al. "Antitumour 2-(4-aminophenyl)benzothiazoles generate DNA adducts in sensitive tumour cells in vitro and in vivo." British Journal of Cancer 88, no. 3 (2003): 470–77. http://dx.doi.org/10.1038/sj.bjc.6600719.

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19

Bradshaw, TD, D.-F. Shi, RJ Schultz, et al. "Influence of 2-(4-aminophenyl)benzothiazoles on growth of human ovarian carcinoma cells in vitro and in vivo." British Journal of Cancer 78, no. 4 (1998): 421–29. http://dx.doi.org/10.1038/bjc.1998.510.

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20

O'Brien, Sean E., Helen L. Browne, Tracey D. Bradshaw, Andrew D. Westwell, Malcolm F. G. Stevens, and Charles A. Laughton. "Antitumor benzothiazoles. Frontier molecular orbital analysis predicts bioactivation of 2-(4-aminophenyl)benzothiazoles to reactive intermediates by cytochrome P4501A1Part 23. For part 22 see Ref. 1." Organic & Biomolecular Chemistry 1, no. 3 (2003): 493–97. http://dx.doi.org/10.1039/b209067h.

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21

SHI, D. F., T. D. BRADSHAW, S. WRIGLEY, et al. "ChemInform Abstract: Antitumor Benzothiazoles. Part 3. Synthesis of 2-(4-Aminophenyl) benzothiazoles and Evaluation of Their Activities Against Breast Cancer Cell Lines in vitro and in vivo." ChemInform 27, no. 49 (2010): no. http://dx.doi.org/10.1002/chin.199649146.

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22

Dhakoniya, Pallavi. "Synthesis and Characterization of Benzylidene Derivatives of Benzothiazole." International Journal for Research in Applied Science and Engineering Technology 9, no. VIII (2021): 506–11. http://dx.doi.org/10.22214/ijraset.2021.37370.

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A series of some novel benzothiazole derivatives were synthesized from the 2-(4-aminophenyl) benzothiazol-5-ol, which was synthesized by the Jacobson method using Lawesson’s reagent. Benzylidene derivatives (P201-P205) were synthesized by catalyzed condensation and acylation method,named as 2-(4-((4 hydroxybenzylidene)amino) phenyl) benzothiazole-5-ol (P201), 2-(4-((4- methoxybenzylidene) amino)phenyl)benzothiazole-5ol(P202),2-(4-((4-chlorobenzylidene) amino)phenyl)benzothiazole-5-ol(P203), (4-((furan-2-ylmethylene) amino)phenyl)benzothiazole-5-ol(P204), Dimethyl(4(5hydroxy benzothiazol2yl)phe

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23

Zhang, Yong, Zhen-Hong Su, Qing-Zhi Wang, and Lei Teng. "2-(4-Aminophenyl)-1,3-benzothiazole." Acta Crystallographica Section E Structure Reports Online 64, no. 11 (2008): o2065. http://dx.doi.org/10.1107/s1600536808031565.

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24

Corrêa, Silviana, Isael Aparecido Rosa, Gustavo A. Andolpho, et al. "Hybrid Materials Based on Magnetic Iron Oxides with Benzothiazole Derivatives: A Plausible Potential Spectroscopy Probe." International Journal of Molecular Sciences 22, no. 8 (2021): 3980. http://dx.doi.org/10.3390/ijms22083980.

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Rare diseases affect a small part of the population, and the most affected are children. Because of the low availability of patients for testing, the pharmaceutical industry cannot develop drugs for the diagnosis of many of these orphan diseases. In this sense, the use of benzothiazole compounds that are highly selective and can act as spectroscopy probes, especially the compound 2-(4′-aminophenyl)benzothiazole (ABT), has been highlighted. This article reports the design of potential contrast agents based on ABT and iron to develop a new material with an efficient mechanism to raise the relaxa

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25

Hacer, Gumus. "Benzothiazole-derived Compound with Antitumor Activıiy: Molecular Structure Determination Using Density Functional Theory (Dft) Method." Annals of Proteomics and Bioinformatics 8, no. 1 (2024): 001–7. http://dx.doi.org/10.29328/journal.apb.1001023.

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The Gaussian computational chemistry software package was employed to investigate the molecular structure and energetics of benzothiazole, a compound known for its anti-tumor properties. Density functional theory (DFT) calculations were conducted using the Becke, 3-parameter, Lee-Yang-Parr (B3LYP) method, coupled with the LanL2DZ basis set. Molecular structure optimization was carried out to determine the most stable configurations of the benzothiazole compound. Furthermore, thorough analyses of molecular orbital energies, molecular properties, and molecular electrostatic potential surface map

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26

Chandni, Jain, Gopal Ram, Panwar Lalita, and Nagar Meena. "Phosphorylation and thiophosphorylation of 2-(4'-aminophenyl)-6-methyl benzothiazole and their biological activities." Journal of Indian Chemical Society 93, June 2016 (2016): 571–75. https://doi.org/10.5281/zenodo.5638395.

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Department of Chemistry, University of Rajasthan, Jaipur-302 004, Rajasthan, India <em>E-mail</em> : nagar_meena@yahoo.com <em>Manuscript received online 15 December 2015, accepted 30 January 2016</em> Some novel organophosphorus compounds of the type [(C<sub>14</sub>H<sub>11</sub>N<sub>2</sub> S)<sub>n</sub>P(O)Cl<sub>3-n</sub>]/[(C<sub>14</sub>H<sub>11</sub>N<sub>2</sub> S)<sub>n</sub>P(S)Cl<sub>3-n</sub>] {where n=1–3} have been easily synthesized by the reaction of 2-(4'-aminophenyl)-6-methyl benzothiazole (C<sub>14</sub>H<sub>11</sub>N<sub>2</sub> S) with phosphorus oxychloride

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27

Reddy, Ragaiahgari Srinivas, Bijaya Ketan Sahoo, Anna Tanuja Safala Bodapati, Shravya Rao Madku, and Kandikonda Lavanya. "Entropy Driven Binding of 2-(4-Aminophenyl)benzothiazole with DNA: An Experimental and Theoretical Insights." Asian Journal of Chemistry 36, no. 12 (2024): 2931–38. https://doi.org/10.14233/ajchem.2024.32874.

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Molecular recognition driven by molecular interactions is an intricate part of drug discovery and targeted drug delivery systems due to the dependence of thetherapeutic properties of drugs on interaction with desired target biomolecules as receptors. 2-(4-Aminophenyl) benzothiazole (APB), a heterocyclic molecule containing a benzothiazole nucleus, is known to induce apoptosis besides inhibiting cancer cell development and has been found effective against different microorganisms. This study highlights the spectroscopic and theoretical investigation of binding interactions of APB and ct-DNA. Th

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28

Kiritsis, Christos, Barbara Mavroidi, Antonio Shegani та ін. "2-(4′-Aminophenyl)benzothiazole Labeled with 99mTc-Cyclopentadienyl for Imaging β-Amyloid Plaques". ACS Medicinal Chemistry Letters 8, № 10 (2017): 1089–92. http://dx.doi.org/10.1021/acsmedchemlett.7b00294.

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29

Bradshaw, T. D., M.-S. Chua, S. Orr, C. S. Matthews, and M. F. G. Stevens. "Mechanisms of acquired resistance to 2-(4-aminophenyl)benzothiazole (CJM 126, NSC 34445)." British Journal of Cancer 83, no. 2 (2000): 270–77. http://dx.doi.org/10.1054/bjoc.2000.1231.

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30

Hu, Wan-Ping, Yin-Kai Chen, Chao-Cheng Liao, et al. "Synthesis, and biological evaluation of 2-(4-aminophenyl)benzothiazole derivatives as photosensitizing agents." Bioorganic & Medicinal Chemistry 18, no. 16 (2010): 6197–207. http://dx.doi.org/10.1016/j.bmc.2010.04.082.

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31

Sukhikh, Taisiya S., Dmitry S. Kolybalov, Ekaterina K. Pylova, and Sergey N. Konchenko. "Luminescent Zn Halide Complexes with 2-(2-Aminophenyl)benzothiazole Derivatives." Inorganics 10, no. 9 (2022): 138. http://dx.doi.org/10.3390/inorganics10090138.

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We report a comparative study of coordination behaviour of 2-(2-aminophenyl)benzothiazole (NH2-pbt) and its phosphorus-containing derivative, α-aminophosphine oxide (PCNH-pbt), towards zinc halides. The corresponding coordination compounds [Zn(L)2Hal2] (L = PCNH-pbt, Hal = Cl, 1 and Hal = Br, 2) and [Zn(L’)Hal2] (L’ = NH2-pbt, Hal = Cl, 3 and Hal = Br, 4) were obtained as single phases. As evidenced by single-crystal X-ray diffraction analysis, L’ ligand coordinates to Zn in a chelate manner via two N atoms. Despite a similar coordination mode in complexes 3 and 4, the spatial geometry of the

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32

Kumar, Abhishek. "Combination And Assessment Of Unique Heterocyclic Compound Subsidiaries Across Human Occipital Disease Unit Lines." American Journal of Medical Sciences and Pharmaceutical Research 2, no. 05 (2020): XI—XIV. http://dx.doi.org/10.37547/tajmspr/volume02issue05-03.

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The 2-arylsubstituted Heterocyclic subordinates were integrated by refluxing o-aminothiophenol with subbed benzoic acids within the sight of polyphosphoric corrosive at 220°. 2Mercaptothiazole was utilized alongside thionyl chloride to get the carbothioates. The physical and unearthly information, for example, mp, Rf, IR, NMR was gotten for the incorporated mixes and the structures were affirmed. The screening for antitumour action was done according to the National Cancer Institute medicate screening procedure 3 mixes were seen as fundamentally cytotoxic when contrasted with [2-(3-bromo-4-ami

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33

Narva, Suresh, Surendar Chitti, Suresh Amaroju, et al. "Design, Synthesis, and Biological Evaluation of 2-(4-Aminophenyl)benzothiazole Analogues as Antiproliferative Agents." Journal of Heterocyclic Chemistry 56, no. 2 (2018): 520–32. http://dx.doi.org/10.1002/jhet.3427.

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34

Tzanopoulou, Stamatia, Marina Sagnou, Maria Paravatou-Petsotas, et al. "Evaluation of Re and99mTc Complexes of 2-(4′-Aminophenyl)benzothiazole as Potential Breast Cancer Radiopharmaceuticals." Journal of Medicinal Chemistry 53, no. 12 (2010): 4633–41. http://dx.doi.org/10.1021/jm1001293.

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35

Yurttaş, Leyla, Funda Tay, and Şeref Demirayak. "Synthesis and antitumor activity evaluation of new 2-(4-aminophenyl)benzothiazole derivatives bearing different heterocyclic rings." Journal of Enzyme Inhibition and Medicinal Chemistry 30, no. 3 (2014): 458–65. http://dx.doi.org/10.3109/14756366.2014.945168.

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36

Lei, De-Qiang, Xing-Li Deng, Hong-Yang Zhao, Fang-Cheng Zhang, and Ru-En Liu. "Inhibition of tumor growth and angiogenesis by 2-(4-aminophenyl) benzothiazole in orthotopicglioma C6 rat model." Saudi Journal of Biological Sciences 25, no. 7 (2018): 1483–87. http://dx.doi.org/10.1016/j.sjbs.2017.04.007.

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37

Lin, Guo-Wu, Yue Wang, Qiao-Mei Jin, et al. "Synthesis, structures and the biological activity study on the metal complexes of 2-(4-aminophenyl)benzothiazole derivative." Inorganica Chimica Acta 382 (March 2012): 35–42. http://dx.doi.org/10.1016/j.ica.2011.10.004.

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38

Mavroidi, Barbara, Marina Sagnou, Kostas Stamatakis, Maria Paravatou-Petsotas, Maria Pelecanou, and Constantinos Methenitis. "Palladium(II) and platinum(II) complexes of derivatives of 2-(4′-aminophenyl)benzothiazole as potential anticancer agents." Inorganica Chimica Acta 444 (April 2016): 63–75. http://dx.doi.org/10.1016/j.ica.2016.01.012.

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39

Dubey, Raghvendra, Prabhat Shrivastava, Pawan Basniwal, Snehendu Bhattacharya, and Narayana Narayana Moorthy. "2-(4-Aminophenyl) Benzothiazole: A Potent and Selective Pharmacophore with Novel Mechanistic Action Towards Various Tumour Cell Lines." Mini-Reviews in Medicinal Chemistry 6, no. 6 (2006): 633–37. http://dx.doi.org/10.2174/138955706777435706.

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40

Mavroidi, B., M. Sagnou, I. Roupa, et al. "Synthesis and evaluation of a fac-[Re(CO)3]+ complex bearing 2-(4’-aminophenyl)benzothiazole as anticancer agent." Nuclear Medicine and Biology 72-73 (July 2019): S50. http://dx.doi.org/10.1016/s0969-8051(19)30327-0.

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41

Wang, Liang, Mengda Niu, Yujia He, Chuanhuizi Tian, Zhiping Peng, and Jianhua Jia. "Synthesis and evaluation of Al18F-NODA complex conjugated 2-(4-aminophenyl)benzothiazole as a potential tumor imaging agent." Bioorganic & Medicinal Chemistry Letters 30, no. 11 (2020): 127160. http://dx.doi.org/10.1016/j.bmcl.2020.127160.

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42

Singh, Meenakshi, Sudhir Kumar Singh, Mayank Gangwar, Satheeshkumar Sellamuthu, Gopal Nath, and Sushil K. Singh. "Design, Synthesis and Mode of Action of Some New 2-(4';-aminophenyl) benzothiazole Derivatives as Potent Antimicrobial Agents." Letters in Drug Design & Discovery 13, no. 5 (2016): 429–37. http://dx.doi.org/10.2174/1570180812666150821003220.

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43

Novak, Michael, and Mrinal Chakraborty. "Reactions of a putative metabolite of the model antitumor drug 2-(4-aminophenyl)benzothiazole with purines and pyrimidines." Journal of Physical Organic Chemistry 24, no. 10 (2011): 960–68. http://dx.doi.org/10.1002/poc.1905.

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44

Mavroidi, Barbara, Marina Sagnou, Eleftherios Halevas, et al. "A Tridentate Cu(II) Complex with a 2-(4′-Aminophenyl)Benzothiazole Derivative: Crystal Structure and Biological Evaluation for Anticancer Activity." Inorganics 11, no. 3 (2023): 132. http://dx.doi.org/10.3390/inorganics11030132.

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Herein, the synthesis, structural characterization and in vitro biological evaluation of a novel Cu(II) complex with the 2-(4-aminophenyl)benzothiazole pharmacophore conjugated with the (2-pyridinyl)methylamino chelating moiety is reported for the first time. A full characterization of the Cu(II) complex was conducted by X-ray crystallography, EPR, IR, elemental and MS analysis, and its binding to CT-DNA was investigated by UV-vis spectroscopy, ethidium bromide competition studies, circular dichroism, viscometry and thermal denaturation. The data clearly indicate that the Cu(II) complex intera

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45

Phillips, Lawrence R., Chris Bramhall, John Buckley, Tracy W. Daw, and Sherman F. Stinson. "Analysis of 2-(3-methyl-4-aminophenyl)-benzothiazole (NSC 674495) in plasma by gas chromatography with mass-selective detection." Journal of Chromatography B: Biomedical Sciences and Applications 732, no. 2 (1999): 315–21. http://dx.doi.org/10.1016/s0378-4347(99)00295-9.

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46

Dey, Joykrishna, Eric L. Roberts та Isiah M. Warner. "Effect of Sodium Perchlorate on the Binding of 2-(4‘-Aminophenyl)- and 2-(4‘-(N,N‘-Dimethylamino)phenyl)benzothiazole with β-Cyclodextrin in Aqueous Solution". Journal of Physical Chemistry A 102, № 1 (1998): 301–5. http://dx.doi.org/10.1021/jp9712260.

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47

Durmaz, Mustafa, Yaser Acikbas, Selahattin Bozkurt, Rifat Capan, Matem Erdogan, and Cansu Ozkaya. "A Novel Calix[4]arene Thiourea Decorated with 2‐(2‐Aminophenyl)benzothiazole Moiety as Highly Selective Chemical Gas Sensor for Dichloromethane Vapor." ChemistrySelect 6, no. 19 (2021): 4670–76. http://dx.doi.org/10.1002/slct.202100631.

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48

Al-Amiery, A. A., A. A. Al-Temimi, A. A. H. Kadhum, et al. "Co-crystal structure of mixed molecules of methyl 2-(3-chloro-4-methyl-2-oxo-2H-chromen-7-yloxy)acetate and 2-(2-aminophenyl)benzothiazole." Journal of Structural Chemistry 54, no. 3 (2013): 648–49. http://dx.doi.org/10.1134/s002247661303030x.

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49

Mourtas, Spyridon, Barbara Mavroidi, Antonia Marazioti та ін. "Liposomes Decorated with 2-(4′-Aminophenyl)benzothiazole Effectively Inhibit Aβ1–42 Fibril Formation and Exhibit in Vitro Brain-Targeting Potential". Biomacromolecules 21, № 12 (2020): 4685–98. http://dx.doi.org/10.1021/acs.biomac.0c00811.

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50

Singh, Meenakshi, Sudhir Kumar Singh, Mayank Gangwar, Gopal Nath, and Sushil K. Singh. "Design, synthesis and mode of action of novel 2-(4-aminophenyl)benzothiazole derivatives bearing semicarbazone and thiosemicarbazone moiety as potent antimicrobial agents." Medicinal Chemistry Research 25, no. 2 (2015): 263–82. http://dx.doi.org/10.1007/s00044-015-1479-5.

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