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Готові списки джерел за темами / 2-mercaptobenzimidazole / Статті в журналах

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Статті в журналах з теми "2-mercaptobenzimidazole"

Автор: Grafiati

Опубліковано: 4 червня 2021

Оновлено: 25 липня 2025

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1

Ravikumar, K., K. Chandra Mohan, M. Bidyasagar, and G. Y. S. K. Swamy. "Crystal structure of 2-mercaptobenzimidazole and bis[2-mercaptobenzimidazole]dichlorocobalt(II)." Journal of Chemical Crystallography 25, no. 6 (1995): 325–29. http://dx.doi.org/10.1007/bf01796058.

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2

Lee, Chang Hwa, John E. Bonevich, Ugo Bertocci, Kristen L. Steffens, and Thomas P. Moffat. "Superconformal Ni Electrodeposition Using 2-Mercaptobenzimidazole." Journal of The Electrochemical Society 158, no. 6 (2011): D366. http://dx.doi.org/10.1149/1.3572055.

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3

Journal, Baghdad Science. "The Preparation of some New Mannich and Shiff bases derived from 2-Mercaptobenzimidazole." Baghdad Science Journal 12, no. 3 (2015): 516–26. http://dx.doi.org/10.21123/bsj.12.3.516-526.

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Анотація:

The present work involved two steps: the first step include Mannich reaction was carried out on 2- mercaptobenzimidazole using formaldehyde and different secondary amine or amide to gives the compounds(2-16). The secnd step include preparation of (Ethylbenzimidazoly-2-mercaptoacetate)(17) from the reaction of 2- mercaptobenzimidazole with ethylchloroacetate than prepared hydrazide derivative[18]from reaction of compound(17) with hydrazinehydrate. Followed Preparation of shiff bases(19-24) and there reaction with mercaptoacetic acid to give a new compounds containing thiazolidinderivetives(25-3

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4

Ahamed, Mohammed R., Shetha F. Narren, and Amaal S. Sadiq. "The Preparation of some New Mannich and Shiff bases derived from 2-Mercaptobenzimidazole." Baghdad Science Journal 12, no. 3 (2015): 516–26. http://dx.doi.org/10.21123/bsj.2015.12.3.516-526.

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Анотація:

The present work involved two steps: the first step include Mannich reaction was carried out on 2- mercaptobenzimidazole using formaldehyde and different secondary amine or amide to gives the compounds(2-16). The secnd step include preparation of (Ethylbenzimidazoly-2-mercaptoacetate)(17) from the reaction of 2- mercaptobenzimidazole with ethylchloroacetate than prepared hydrazide derivative[18]from reaction of compound(17) with hydrazinehydrate. Followed Preparation of shiff bases(19-24) and there reaction with mercaptoacetic acid to give a new compounds containing thiazolidinderivetives(25-3

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5

Doneux, Th, M. Steichen, T. Bouchta, and Cl Buess-Herman. "Mixed self-assembled monolayers of 2-mercaptobenzimidazole and 2-mercaptobenzimidazole-5-sulfonate: Determination and control of the surface composition." Journal of Electroanalytical Chemistry 599, no. 2 (2007): 241–48. http://dx.doi.org/10.1016/j.jelechem.2006.03.006.

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6

Gezerman, Ahmet Ozan, and Burcu Didem Çorbacıoğlu. "2-Mercaptobenzimidazole, 2-Mercaptobenzothiazole, and Thioglycolic Acid in an Electroless Nickel-Plating Bath." Journal of Chemistry 2015 (2015): 1–11. http://dx.doi.org/10.1155/2015/872516.

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The use of three different materials, 2-mercaptobenzimidazole, 2-mercaptobenzothiazole, and thioglycolic acid, was investigated to improve the performance of electroless nickel-plating baths. By changing the concentrations of these materials, sample plates were coated. Optical microscope images were obtained by selecting representative coated plates. From the results of the investigations, the effects of these materials on electroless nickel plating were observed, and the most appropriate amounts of these materials for nickel plating were determined. Moreover, the nickel plating speed observed

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7

Kaim, Vishakha, and Sandeep Kaur-Ghumaan. "Mononuclear Mn complexes featuring N,S-/N,N-donor and 1,3,5-triaza-7-phosphaadamantane ligands: synthesis and electrocatalytic properties." New Journal of Chemistry 45, no. 43 (2021): 20272–79. http://dx.doi.org/10.1039/d1nj02104d.

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Mononuclear Mn(i) carbonyl complexes incorporating 2-mercaptobenzothiazole or 2-mercaptobenzimidazole and phosphaadamantane ligands were evaluated as electrocatalysts for the HER both in acetonitrile and acetonitrile/water.

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8

Marathe, Ravindra J., Ashok B. Chaudhari, Rahul K. Hedaoo, Daewon Sohn, Vijay R. Chaudhari, and Vikas V. Gite. "Urea formaldehyde (UF) microcapsules loaded with corrosion inhibitor for enhancing the anti-corrosive properties of acrylic-based multi-functional PU coatings." RSC Advances 5, no. 20 (2015): 15539–46. http://dx.doi.org/10.1039/c4ra16327c.

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Анотація:

The present work focuses on enhancing the anti-corrosive performance of multi-functional PU coatings by encapsulation of the commercial inhibitors 2-mercaptobenzimidazole & 2-mercapatobenzothiozole, despite their reaction with diisocyanate.

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9

Das, Arup Jyoti, Hemi Borgohain, Bipul Sarma, and Sajal Kumar Das. "Switching of regioselectivity in base-mediated diastereoselective annulation of 2,3-epoxy tosylates and their N-tosylaziridine analogs with 2-mercaptobenzimidazole." Organic & Biomolecular Chemistry 18, no. 3 (2020): 441–49. http://dx.doi.org/10.1039/c9ob02454a.

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10

O. Abdelhamid, Abdou, and Cyril P�k�yi. "Photodegradation of Pesticides: Photolysis of 2-Mercaptobnzothiaozle and 2-Mercaptobenzimidazole." HETEROCYCLES 23, no. 11 (1985): 2917. http://dx.doi.org/10.3987/r-1985-11-2917.

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11

El-Shaieb, Kamal M. "Reaction of Dimethyl Acetylenedicarboxylate With 2-Mercaptoperimidine and 2-Mercaptobenzimidazole." Phosphorus, Sulfur, and Silicon and the Related Elements 181, no. 3 (2006): 675–81. http://dx.doi.org/10.1080/10426500500269950.

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12

Silva, Ana L. R., and Maria D. M. C. Ribeiro da Silva. "Energetic, structural and tautomeric analysis of 2-mercaptobenzimidazole." Journal of Thermal Analysis and Calorimetry 129, no. 3 (2017): 1679–88. http://dx.doi.org/10.1007/s10973-017-6353-x.

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13

Journal, Baghdad Science. "Synthesis of Some New 1,2,4-Triazoles Derived from 2-Mercaptobenzimidazole." Baghdad Science Journal 6, no. 1 (2009): 200–208. http://dx.doi.org/10.21123/bsj.6.1.200-208.

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Анотація:

New 1,2,4-triazole derivatives of 2-mercaptobenzimidazole (MB) are reported. Ethyl (benzimidazole-2-yl thio) acetate (1) has been prepared by condensing 2-mercaptobenzimidazole with ethylchloroacetate. The ester (1) on reacting with hydrazine hydrate gave the corresponding acetohydrazide(2)which was reacted separately with phenylisocyanate and phenylisothiocyanate, followed by ring closure in an alkaline medium giving 3-[(benzimidazole-2-yl thio) methyl]-4-phenyl-1,2,4-triazole-5-ol and 3-[(benzimidazole-2-yl thio) methyl]-4-phenyl-1,2,4-triazole-5-thiol respectively (6,7). Reaction of acetohy

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14

Al-Messri, Zainab, A. K. "Synthesis of Some New 1,2,4-Triazoles Derived from 2-Mercaptobenzimidazole." Baghdad Science Journal 6, no. 1 (2009): 200–208. http://dx.doi.org/10.21123/bsj.2009.6.1.200-208.

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Анотація:

New 1,2,4-triazole derivatives of 2-mercaptobenzimidazole (MB) are reported. Ethyl (benzimidazole-2-yl thio) acetate (1) has been prepared by condensing 2-mercaptobenzimidazole with ethylchloroacetate. The ester (1) on reacting with hydrazine hydrate gave the corresponding acetohydrazide(2)which was reacted separately with phenylisocyanate and phenylisothiocyanate, followed by ring closure in an alkaline medium giving 3-[(benzimidazole-2-yl thio) methyl]-4-phenyl-1,2,4-triazole-5-ol and 3-[(benzimidazole-2-yl thio) methyl]-4-phenyl-1,2,4-triazole-5-thiol respectively (6,7). Reaction of acetohy

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15

Han, Song-De, Xiao-Hong Miao, Sui-Jun Liu, and Xian-He Bu. "A series of cobalt and nickel clusters based on thiol-containing ligands accompanied by in situ ligand formation." Dalton Transactions 44, no. 2 (2015): 560–67. http://dx.doi.org/10.1039/c4dt03109a.

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Анотація:

We report a series of cobalt and nickel clusters based on thiol-containing ligands, 2-mercaptobenzothiazole (HMBT) and 2-mercaptobenzimidazole (H<sub>2</sub>MBI), accompanied by in situ ligand transformation of HMBT. The magnetic properties of the cobalt clusters have been investigated.

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16

Singh, Suryabhan, and Subrato Bhattacharya. "Studies of structural diversity due to inter-/intra-molecular hydrogen bonding and photoluminescent properties in thiocarboxylate Cu(i) and Ag(i) complexes." RSC Adv. 4, no. 90 (2014): 49491–500. http://dx.doi.org/10.1039/c4ra07883g.

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Cu(I) and Ag(I) thiocarboxylate complexes containing 2-mercaptobenzimidazole and 2-mercapto-2-thiazoline were synthesized. Direction of H-bonding depends on the R-group of thiocarboxylate ligands. AIM and NBO (DFT) calculations revealed the nature of M-M interactions in complex 7.

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17

Amini, M. K., A. Rafi, and I. Mohammadpoor-Baltork. "SILVER-SELECTIVE MEMBRANE ELECTRODES USING 2-MERCAPTOBENZIMIDAZOLE AND 2-MERCAPTOBENZOTHIAZOLE CARRIERS." Analytical Letters 35, no. 11 (2002): 1795–809. http://dx.doi.org/10.1081/al-120013584.

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18

ISAMA, Kazuo, Masaaki KANIWA, and Akitada NAKAMURA. "Analysis of 2-Mercaptobenzimidazole Type Antioxidants in Rubber Products." Eisei kagaku 44, no. 2 (1998): 99–106. http://dx.doi.org/10.1248/jhs1956.44.99.

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19

Trachli, B., M. Keddam, H. Takenouti, and A. Srhiri. "Protective effect of electropolymerized 2-mercaptobenzimidazole upon copper corrosion." Progress in Organic Coatings 44, no. 1 (2002): 17–23. http://dx.doi.org/10.1016/s0300-9440(01)00205-3.

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20

Ahamed, Mohammed R., Shetha F. Narren, and Amal S. Sadiq. "Synthesis of 2-Mercaptobenzimidazole and Some of its Derivatives." Journal of Al-Nahrain University Science 16, no. 2 (2013): 77–83. http://dx.doi.org/10.22401/jnus.16.2.11.

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21

Doneux, T., C. Buess-Herman, M. G. Hosseini, R. J. Nichols, and J. Lipkowski. "Adsorption of 2-mercaptobenzimidazole on a Au(111) electrode." Electrochimica Acta 50, no. 21 (2005): 4275–82. http://dx.doi.org/10.1016/j.electacta.2005.01.063.

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22

Ryaskina, E. V., M. V. Voronin, and S. B. Seredenin. "Interaction of 2-mercaptobenzimidazole derivatives with sigma-1 receptors." Pharmaceutical Chemistry Journal 46, no. 6 (2012): 334–36. http://dx.doi.org/10.1007/s11094-012-0793-1.

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23

Mazloum, Mohammad, Mohammad K. Amini, and Iraj Mohammadpoor-Baltork. "Mercury selective membrane electrodes using 2-mercaptobenzimidazole, 2-mercaptobenzothiazole, and hexathiacyclooctadecane carriers." Sensors and Actuators B: Chemical 63, no. 1-2 (2000): 80–85. http://dx.doi.org/10.1016/s0925-4005(00)00300-2.

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24

Muhammad Yousaf, Muhammad Yousaf, Momin Khan Momin Khan, Mumtaz Ali Mumtaz Ali, et al. "2-Mercaptobenzimidazole Derivatives as Novel Butyrylcholinesterase Inhibitors: Biology-Oriented Drug Synthesis (BIODS), In-Vitro and In-Silico Evaluation." Journal of the chemical society of pakistan 42, no. 2 (2020): 263. http://dx.doi.org/10.52568/000627/jcsp/42.02.2020.

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Schiff bases gaining remarkable importance day by day in the current situation Schiff bases are found to be a valuable pharmacophore for the synthesis and development of various biologically active heterocyclic compounds. In recent past, we have reported various classes of compounds as enzyme inhibitors, in continuation; A series of 2-Mercaptobenzimidazole hydrazone derivatives (9-42) were synthesized through multistep reactions in high yields and evaluated for butyrylcholinesterase inhibition. In present study, 2-ethylthio benzimidazole was formed by the reaction of 2-Mercaptobenzimidazole wi

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25

Cesarino, Ivana, Glimaldo Marino, Éder T. G. Cavalheiro, Regina F. Nogueira, and Antonio G. Ferreira. "Preparation and Characterization of Amorphous Silica Organofunctionalised with 2-Mercaptobenzimidazole." Materials Science Forum 636-637 (January 2010): 793–97. http://dx.doi.org/10.4028/www.scientific.net/msf.636-637.793.

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Organofunctionalised silica materials are of great interest once they combine a high surface area and a narrow pore size distribution with the advantage of owing organic ligand properties. This paper describes the organofunctionalisation of an amorphous silica with 2-mercaptobenzimidazole. The characterization of such material was performed by elemental analysis (EA), IR spectroscopy, thermogravimetry (TG), differential scanning calorimetry (DSC) and solid state 13C and 29Si NMR spectroscopy.

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26

Chupakhina, T. A., and V. O. Kur’yanov. "Specific Features of Phase Transfer Catalytic Glycosylation of 2-Mercaptobenzimidazole." Russian Journal of Bioorganic Chemistry 46, no. 6 (2020): 1285–88. http://dx.doi.org/10.1134/s1068162020060047.

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27

Petko, Kirill I., Yurii G. Vlasenko, and Oleksii D. Kachkovskii. "Unexpected “reverse” cyclization of 2-mercaptobenzimidazole with chlorotrifluoroethylene and hexafluoropropene." Journal of Fluorine Chemistry 185 (May 2016): 168–72. http://dx.doi.org/10.1016/j.jfluchem.2016.03.006.

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28

Teo, Yong-Chua, and Bryan Tan. "Ligand-Free CuI-Catalyzed Chemoselective S-Arylation of 2-Mercaptobenzimidazole with Aryl Iodides." Synlett 29, no. 15 (2018): 2056–60. http://dx.doi.org/10.1055/s-0037-1610655.

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Анотація:

A practical and efficient strategy for the chemoselective C–S cross-coupling of 2-mercaptobenzimidazole derivatives with a range of substituted aryl iodides is described. Under the optimized conditions of 5 mol% CuI and 100 °C, a variety of S-arylated products were obtained in good to excellent yields (up to 92 %) without the need for assisting ligands.

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29

Tahlan, Sumit, Balasubramanian Narasimhan, Siong Meng Lim, Kalavathy Ramasamy, Vasudevan Mani, and Syed A. A. Shah. "2-Mercaptobenzimidazole Schiff Bases: Design, Synthesis, Antimicrobial Studies and Anticancer Activity on HCT-116 Cell Line." Mini-Reviews in Medicinal Chemistry 19, no. 13 (2019): 1080–92. http://dx.doi.org/10.2174/1389557518666181009151008.

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Background: Increased rate of mortality due to the development of resistance to currently available antimicrobial and anticancer agents initiated the need to develop new chemical entities for the treatment of microbial infections and cancer. Objective: The present study was aimed to synthesize and evaluate antimicrobial and anticancer activities of Schiff bases of 2-mercaptobenzimidazole. Methods: The Schiff bases of 2-mercaptobenzimidazole were synthesized from 4-(2-(1H-benzo[d]- imidazol-2-ylthio)acetamido)benzohydrazide. The synthesized compounds were evaluated for antimicrobial and antican

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30

A. Porto, Viviane, Paulo R. S. Correia, and Ricardo S. Porto. "Synthesis and Antibacterial Activity of 2-Mercaptobenzimidazole Derivatives: A Literature Review." Revista Virtual de Química 13, no. 6 (2021): 1457–66. http://dx.doi.org/10.21577/1984-6835.20210081.

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31

Voronin, Mikhail V., Ilya A. Kadnikov, Liana F. Zainullina, et al. "Neuroprotective Properties of Quinone Reductase 2 Inhibitor M-11, a 2-Mercaptobenzimidazole Derivative." International Journal of Molecular Sciences 22, no. 23 (2021): 13061. http://dx.doi.org/10.3390/ijms222313061.

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The ability of NQO2 to increase the production of free radicals under enhanced generation of quinone derivatives of catecholamines is considered to be a component of neurodegenerative disease pathogenesis. The present study aimed to investigate the neuroprotective mechanisms of original NQO2 inhibitor M-11 (2-[2-(3-oxomorpholin-4-il)-ethylthio]-5-ethoxybenzimidazole hydrochloride) in a cellular damage model using NQO2 endogenous substrate adrenochrome (125 µM) and co-substrate BNAH (100 µM). The effects of M-11 (10–100 µM) on the reactive oxygen species (ROS) generation, apoptosis and lesion o

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32

GAWORSKI, CHARLES L., CATHERINE ARANYI, STANLEY VANA, et al. "Prechronic Inhalation Toxicity Studies of 2-Mercaptobenzimidazole (2-MBI)in F344/N Rats." Toxicological Sciences 16, no. 1 (1991): 161–71. http://dx.doi.org/10.1093/toxsci/16.1.161.

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33

Gezerman, Ahmet Ozan, and Burcu Didem Çorbacıoğlu. "2-Mercaptobenzimidazole, 2-Mercaptobenzothiazole, and Thioglycolic Acid as Additives for Electrolytic Ni Plating." Iranian Journal of Science and Technology, Transactions A: Science 42, no. 2 (2016): 465–75. http://dx.doi.org/10.1007/s40995-016-0142-4.

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34

Vernack, Eléa, Dominique Costa, Philippe Tingaut, and Philippe Marcus. "DFT studies of 2-mercaptobenzothiazole and 2-mercaptobenzimidazole as corrosion inhibitors for copper." Corrosion Science 174 (September 2020): 108840. http://dx.doi.org/10.1016/j.corsci.2020.108840.

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35

Alizadeh, Abdolali, and Akram Bagherinejad. "Synthesis of 2‐ O ‐Functionalized‐5‐salicyloyl Pyridine Derivatives Catalyzed by 2‐Mercaptobenzimidazole." ChemistrySelect 5, no. 45 (2020): 14303–6. http://dx.doi.org/10.1002/slct.202003748.

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36

Liu, Jing, Xiaozong Dou, and Hongyan Zhang. "2-Mercaptobenzimidazole Functionalized Copper Nanoparticles Fluorescence Probe for Sensitivity and Selectivity Detection of Cys in Serum." Sensors 23, no. 13 (2023): 5814. http://dx.doi.org/10.3390/s23135814.

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Анотація:

In this paper, a 2-mercaptobenzimidazole-copper nanoparticles (MBI-CuNPs) fluorescent probe with high performance based on 2-mercaptobenzimidazole functionalized copper nanoparticles was synthesized by a hydrothermal method and used for cysteine (Cys) detection in serum. The MBI-CuNPs probe exhibits strong fluorescence emission at 415 nm under the excitation at 200 nm, which is attributed to the metal-ligand charge transfer (MLCT) transition through the coordination of an MBI ligand and monovalent copper. Furthermore, the MBI-CuNPs probe has a high quenching fluorescence response to Cys, and s

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37

Asea, Philip E., James D. MacNeil, and Joe O. Boison. "An Analytical Method to Screen for Six Thyreostatic Drug Residues in the Thyroid Gland andMuscle Tissues of Food Producing Animals by Liquid Chromatography with Ultraviolet Absorption Detection and Liquid Chromatography/Mass Spectrometry." Journal of AOAC INTERNATIONAL 89, no. 2 (2006): 567–75. http://dx.doi.org/10.1093/jaoac/89.2.567.

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Abstract A method was developed and validated to screen for residues of the thyreostatic drugs, tapazole (TAP), mercaptobenzimidazole (MBI), thiouracil (TU), methylthiouracil (MTU), propylthiouracil (PrTU), and phenylthiouracil (PhTU) in bovine, equine, ovine, and porcine thyroid and muscle tissues at concentrations 5 ng/g using 2-methoxy-mercaptobenzimidazole (MeMBI) and dimethylthiouracil (DMTU) as internal standards. In this method, the drugs were solvent extracted from thyroid and muscle tissue and cleaned up on an amino-propyl solid-phase extraction (SPE) cartridge. The unretained fractio

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38

Safarmamadov, Safarmamad Muborakshoevich, Zamira Ismatulloevna Karimova, Kimyo Sabzkadam Mabatkadamzoda, Usuf Faizulloevich Bahodurov, and Anjuman Sadriddinovna Sodatdinova. "STABILITY OF 2- MERCAPTOBENZIMIDAZOLE SILVER (I) COMPLEXES IN WATER-METHANOL SOLUTIONS." Вестник Таджикского национального университета. Серия естественных наук, no. 2 (2020): 168–77. http://dx.doi.org/10.51884/2413-452x_2020_2_168.

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39

Ramazanova, Patimat A., Raisa M. Gadzhimuradova, Abdusalam M. M. Ali, Khadizhat A. Magomedova, and Khidirlas S. Khibiev. "Study of the Reaction Centers of 2-mercaptobenzimidazole in Alkylation Reactions." Dagestan State Pedagogical University. Journal. Natural and Exact Sciences 12, no. 1 (2018): 25–31. http://dx.doi.org/10.31161/1995-0675-2018-12-1-25-31.

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40

Devi, Poonam, Mohammad Shahnaz, and D. N. Prasad. "Recent Overview on Synthesis of 2-Mercaptobenzimidazole Derivatives and its Activities." Journal of Drug Delivery and Therapeutics 12, no. 1 (2022): 203–7. http://dx.doi.org/10.22270/jddt.v12i1.5166.

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A novel series 2-(1H-benzimidazol-2-ylsulfanyl) -N-(4-oxo-2-phenyl-thiazolidin-3yl) Various aldehydes and 2-acetamides have been used to synthesise -acetamide 5a–j (5-phenyl-[1,3,4]-oxadiazol-2-ylmethylsulfanyl) - 1H-benzimidazole 6a–j derived from a variety of benzoic acids. These compounds were tested in vitro for antibacterial activity against Gram positive bacteria Staphylococcus aureus and Enterococcus faecalis, Gram negative bacteria Klebsiella pneumoniae and Escherichia coli, and antifungal activity against Aspergillus fumigatus and Candida albicans. The in vitro cytotoxic properties of

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