Статті в журналах з теми "Benzamidine analogues"
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Fouda, A. S., M. A. Ismail, A. S. Abousalem, and G. Y. Elewady. "Experimental and theoretical studies on corrosion inhibition of 4-amidinophenyl-2,2′-bifuran and its analogues in acidic media." RSC Adv. 7, no. 73 (2017): 46414–30. http://dx.doi.org/10.1039/c7ra08092a.
Повний текст джерелаSa’ad, Mohammad Auwal, Ramasamy Kavitha, Shivkanya Fuloria, Neeraj Kumar Fuloria, Manickam Ravichandran, and Pattabhiraman Lalitha. "Synthesis, Characterization and Biological Evaluation of Novel Benzamidine Derivatives: Newer Antibiotics for Periodontitis Treatment." Antibiotics 11, no. 2 (February 7, 2022): 207. http://dx.doi.org/10.3390/antibiotics11020207.
Повний текст джерелаAtassi, M. Z. "Surface-simulation synthesis of the substrate-binding site of an enzyme. Demonstration with trypsin." Biochemical Journal 226, no. 2 (March 1, 1985): 477–85. http://dx.doi.org/10.1042/bj2260477.
Повний текст джерелаKalinichenko, Elena, Aliaksandr Faryna, Viktoria Kondrateva, Alena Vlasova, Valentina Shevchenko, Alla Melnik, Olga Avdoshko, and Alla Belko. "Synthesis, Biological Activities and Docking Studies of Novel 4-(Arylaminomethyl)benzamide Derivatives as Potential Tyrosine Kinase Inhibitors." Molecules 24, no. 19 (September 30, 2019): 3543. http://dx.doi.org/10.3390/molecules24193543.
Повний текст джерелаVeselinović, Aleksandar M., Andrey Toropov, Alla Toropova, Dobrila Stanković-Đorđević, and Jovana B. Veselinović. "Design and development of novel antibiotics based on FtsZ inhibition – in silico studies." New Journal of Chemistry 42, no. 13 (2018): 10976–82. http://dx.doi.org/10.1039/c8nj01034j.
Повний текст джерелаSugano, Kiyohiko, Shoshin Yoshida, Mikio Takaku, Masayuki Haramura, Ryoichi Saitoh, Yoshiaki Nabuchi, and Hidetoshi Ushio. "Quantitative structure–intestinal permeability relationship of benzamidine analogue thrombin inhibitor." Bioorganic & Medicinal Chemistry Letters 10, no. 17 (September 2000): 1939–42. http://dx.doi.org/10.1016/s0960-894x(00)00367-x.
Повний текст джерелаElkamhawy, Ahmed, Na Kyoung Oh, Noha A. Gouda, Magda H. Abdellattif, Saud O. Alshammari, Mohammed A. S. Abourehab, Qamar A. Alshammari, et al. "Novel Hybrid Indole-Based Caffeic Acid Amide Derivatives as Potent Free Radical Scavenging Agents: Rational Design, Synthesis, Spectroscopic Characterization, In Silico and In Vitro Investigations." Metabolites 13, no. 2 (January 17, 2023): 141. http://dx.doi.org/10.3390/metabo13020141.
Повний текст джерелаBalkrishna, Shah Jaimin, Shailesh Kumar, Gajendra Kumar Azad, Bhagat Singh Bhakuni, Piyush Panini, Navjeet Ahalawat, Raghuvir Singh Tomar, Michael R. Detty, and Sangit Kumar. "An ebselen like catalyst with enhanced GPx activity via a selenol intermediate." Org. Biomol. Chem. 12, no. 8 (2014): 1215–19. http://dx.doi.org/10.1039/c4ob00027g.
Повний текст джерелаOng, Xandria, Manan Ahmed, Luonan Xu, Ashley T. Brennan, Carol Hua, Katrina A. Zenere, Zixi Xie, Cameron J. Kepert, Benjamin J. Powell, and Suzanne M. Neville. "Spin-Crossover 2-D Hofmann Frameworks Incorporating an Amide-Functionalized Ligand: N-(pyridin-4-yl)benzamide." Chemistry 3, no. 1 (March 1, 2021): 360–72. http://dx.doi.org/10.3390/chemistry3010026.
Повний текст джерелаSugano, Kiyohiko, Shoshin Yoshida, Mikio Takaku, Masayuki Haramura, Ryoichi Saitoh, Yoshiaki Nabuchi, and Hidetoshi Ushio. "Corrigendum to “Quantitative structure–Intestinal permeability relationship of benzamidine analogue thrombin inhibitor”." Bioorganic & Medicinal Chemistry Letters 11, no. 8 (April 2001): 1097. http://dx.doi.org/10.1016/s0960-894x(01)00121-4.
Повний текст джерелаMondal, Pradip Kumar, Rahul Shukla, Subha Biswas, and Deepak Chopra. "Role of halogen-involved intermolecular interactions and existence of isostructurality in the crystal packing of —CF3 and halogen (Cl or Br or I) substituted benzamides." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 74, no. 6 (November 14, 2018): 574–91. http://dx.doi.org/10.1107/s2052520618013422.
Повний текст джерелаSlavíková, Barbora, Alexander Kasal та Ladislav Kohout. "N-Benzoyl-N-methylandrostan-17β-amines; 20-Aza Analogues of Brassinolide". Collection of Czechoslovak Chemical Communications 63, № 5 (1998): 655–61. http://dx.doi.org/10.1135/cccc19980655.
Повний текст джерелаCollin, Sonia, Florence Moureau, Mirna Gil Quintero, Daniel P. Vercauteren, Guy Evrard, and Fran�ois Durant. "Stereoelectronic requirements of benzamide 5HT3 antagonists. Comparison with D2 antidopaminergic analogues." Journal of the Chemical Society, Perkin Transactions 2, no. 1 (1995): 77. http://dx.doi.org/10.1039/p29950000077.
Повний текст джерелаMach, Robert H., Yunsheng Huang, Rebekah A. Freeman, Li Wu, Suwanna Vangveravong та Robert R. Luedtke. "Conformationally-flexible benzamide analogues as dopamine D3 and σ2 receptor ligands". Bioorganic & Medicinal Chemistry Letters 14, № 1 (січень 2004): 195–202. http://dx.doi.org/10.1016/j.bmcl.2003.09.083.
Повний текст джерелаMariani, Alberto, Sabina L. E. Mazzanti, and Saverio Russo. "Role of the reaction parameters in the direct synthesis of aromatic polyamides." Canadian Journal of Chemistry 73, no. 11 (November 1, 1995): 1960–65. http://dx.doi.org/10.1139/v95-242.
Повний текст джерелаLi, Jin, Qinggang Meng, Yang Lei, Bing Gu, Yu Liu, and Weiyue Lu. "Benzamide analogue-conjugated polyethylenimine for brain-targeting and gene delivery." Journal of Drug Targeting 19, no. 9 (October 14, 2011): 814–20. http://dx.doi.org/10.3109/1061186x.2011.572975.
Повний текст джерелаBrown, J. M., M. J. Lemmon, M. R. Horsman, and W. W. Lee. "Structure–activity Relationships for Tumour Radiosensitization by Analogues of Nicotinamide and Benzamide." International Journal of Radiation Biology 59, no. 3 (January 1991): 739–48. http://dx.doi.org/10.1080/09553009114550651.
Повний текст джерелаNader, M. A., K. L. Green, R. R. Luedtke, and R. H. Mach. "The effects of benzamide analogues on cocaine self-administration in rhesus monkeys." Psychopharmacology 147, no. 2 (November 19, 1999): 143–52. http://dx.doi.org/10.1007/s002130051154.
Повний текст джерелаHatano, Kentaro, Tastuo Ido, Kiichi Ishiwata, Koichiro Kawashiroa, Jun Hatazawa, Masatoshi Itoh, and Ren Iwata. "Synthesis of [18F]fluoroalkylated analogues of a benzamide nuroleptic; YM-09151-2." Journal of Labelled Compounds and Radiopharmaceuticals 26, no. 1-12 (January 1989): 329–31. http://dx.doi.org/10.1002/jlcr.25802601142.
Повний текст джерелаHorsman, MR, and DJ Chaplin. "Enhancement of cyclophosphamide cytotoxicity in vivo by the benzamide analogue pyrazinamide." British Journal of Cancer 69, no. 4 (April 1994): 648–54. http://dx.doi.org/10.1038/bjc.1994.126.
Повний текст джерелаZhang, Qing-Wei, and Jian-Qi Li. "Synthesis and Biological Evaluation of N-(Aminopyridine) Benzamide Analogues as Histone Deacetylase Inhibitors." Bulletin of the Korean Chemical Society 33, no. 2 (February 20, 2012): 535–40. http://dx.doi.org/10.5012/bkcs.2012.33.2.535.
Повний текст джерелаJørgensen, Charlotte G., Bente Frølund, Jan Kehler, and Anders A. Jensen. "Discovery of Benzamide Analogues as a Novel Class of 5-HT3 Receptor Agonists." ChemMedChem 6, no. 4 (January 18, 2011): 725–36. http://dx.doi.org/10.1002/cmdc.201000444.
Повний текст джерелаJanabi, Mustafa, Catherine M. Pollock, Ann-Marie Chacko, and Duncan H. Hunter. "Resin-supported arylstannanes as precursors for radiolabeling with iodine: benzaldehydes, benzoic acids, benzamides, and NHS esters." Canadian Journal of Chemistry 93, no. 2 (February 2015): 207–17. http://dx.doi.org/10.1139/cjc-2014-0265.
Повний текст джерелаChaplin, DJ, MJ Trotter, KA Skov, and MR Horsman. "Modification of tumour radiation response in vivo by the benzamide analogue pyrazinamide." British Journal of Cancer 62, no. 4 (October 1990): 561–66. http://dx.doi.org/10.1038/bjc.1990.330.
Повний текст джерелаŠmidrkal, Jan, Jiří Holubek, and Jan Trojánek. "The synthesis of 2,3,7,8-bismethylenedioxy-11-methoxy-5-methylbenzo[c]phenanthridinium chloride." Collection of Czechoslovak Chemical Communications 50, no. 4 (1985): 984–90. http://dx.doi.org/10.1135/cccc19850984.
Повний текст джерелаAhsan, Mohamed Jawed, Rupesh Kumar Kumawat, Surender Singh Jadav, Mohammed H. Geesi, Mohammed Afroz Bakht, Mohd Zaheen Hassan, Abdulmalik Bin Saleh Al-Tamimi, et al. "Synthesis, Cytotoxic Evaluation, and Molecular Docking Studies of N-(7- hydroxy-4-methyl-2-oxoquinolin-1(2H)-yl)acetamide/benzamide Analogues." Letters in Drug Design & Discovery 16, no. 2 (November 29, 2018): 182–93. http://dx.doi.org/10.2174/1570180815666180501160047.
Повний текст джерелаCollin, Sonia, Daniel P. Vercauteren, Guy Evrard, and Fran�ois Durant. "Molecular structure analysis of benzamide neuroleptics. Part 13. A tropapride sulphonamidic analogue C15H22N3O3SCl." Journal of the Chemical Society, Perkin Transactions 2, no. 5 (1989): 407. http://dx.doi.org/10.1039/p29890000407.
Повний текст джерелаElaut, G., G. Laus, P. Papeleu, V. Breckx, J. Van Hemel, M. Erra, G. Brosch, et al. "284 Benzamide-based trichostatin a analogues are potent and metabolically stable inhibitors of histone deacetylase." Toxicology Letters 144 (September 2003): s78. http://dx.doi.org/10.1016/s0378-4274(03)90283-9.
Повний текст джерелаSestili, P., C. Balsmini, G. Spadoni, F. Cattabeni, and O. Cantoni. "Analogues of benzamide as poly(ADP-ribose)transferase inhibitors: A study on structure activity relationships." Pharmacological Research Communications 20, no. 7 (July 1988): 613–14. http://dx.doi.org/10.1016/s0031-6989(88)80091-2.
Повний текст джерелаBatool, Farhana, Maria A. Khan, Nimra N. Shaikh, Shazia Iqbal, Shahida Akbar, Saba Fazal‐ur‐rehman, Muhammad Iqbal Choudhary та Fatima Z. Basha. "New Benzamide Analogues of Metronidazole‐tethered Triazoles as Non‐sugar Based Inhibitors of β ‐Glucuronidase". ChemistrySelect 4, № 29 (5 серпня 2019): 8634–37. http://dx.doi.org/10.1002/slct.201901870.
Повний текст джерелаWadhwa, Pankaj, Priti Jain, Arpit Patel, Shantanu Shinde, and Hemant R. Jadhav. "Synthesis and Evaluation of 3-(1,3-dioxoisoindolin-2-yl)-N-substituted Phenyl Benzamide Analogues as HIV Integrase Strand Transfer Inhibitors." Anti-Infective Agents 17, no. 2 (July 5, 2019): 105–14. http://dx.doi.org/10.2174/2211352516666181102121920.
Повний текст джерелаPankiewicz, Krzysztof W., and Krzysztof Felczak. "From ribavirin to NAD analogues and back to ribavirin in search for anticancer agents." Heterocyclic Communications 21, no. 5 (October 1, 2015): 249–57. http://dx.doi.org/10.1515/hc-2015-0133.
Повний текст джерелаAntolini, Floria, Peter B. Hitchcock, Alexei V. Khvostov, and Michael F. Lappert. "Synthesis and characterization of N-silylated, C1-symmetric benzamidinates of lithium, sodium, and tin(II)." Canadian Journal of Chemistry 84, no. 2 (February 1, 2006): 269–76. http://dx.doi.org/10.1139/v05-250.
Повний текст джерелаRosenberg, Claudio L., and Mark R. Handy. "Syntectonic melt pathways during simple shearing of a partially molten rock analogue (Norcamphor-Benzamide)." Journal of Geophysical Research: Solid Earth 105, B2 (February 10, 2000): 3135–49. http://dx.doi.org/10.1029/1999jb900371.
Повний текст джерелаSingh, Sukhbir, Sandeep Arora, Ervon Dhalio, Neelam Sharma, Kunal Arora, and Ajmer Singh Grewal. "Design and synthesis of newer N-benzimidazol-2yl benzamide analogues as allosteric activators of human glucokinase." Medicinal Chemistry Research 30, no. 3 (January 13, 2021): 760–70. http://dx.doi.org/10.1007/s00044-020-02697-z.
Повний текст джерелаSwarna, Venkat Manoj, Bradley J. Undem, and Vijaya L. Korlipara. "Design and synthesis of 3,5-disubstituted benzamide analogues of DNK333 as dual NK1/NK2 receptor probes." Bioorganic & Medicinal Chemistry Letters 17, no. 4 (February 2007): 890–94. http://dx.doi.org/10.1016/j.bmcl.2006.11.064.
Повний текст джерелаJayaram, Hiremagalur N., Michael Grusch, David A. Cooney, and Georg Krupitza. "Consequences of IMP Dehydrogenase Inhibition, and its Relationship to Cancer and Apoptosis." Current Medicinal Chemistry 6, no. 7 (July 1999): 561–74. http://dx.doi.org/10.2174/092986730607220401122851.
Повний текст джерелаSrinivasarao, Singireddi, Adinarayana Nandikolla, Amaroju Suresh, Kevin Van Calster, Linda De Voogt, Davie Cappoen, Balaram Ghosh, Himanshu Aggarwal, Sankaranarayanan Murugesan, and Kondapalli Venkata Gowri Chandra Sekhar. "Seeking potent anti-tubercular agents: design and synthesis of substituted-N-(6-(4-(pyrazine-2-carbonyl)piperazine/homopiperazine-1-yl)pyridin-3-yl)benzamide derivatives as anti-tubercular agents." RSC Advances 10, no. 21 (2020): 12272–88. http://dx.doi.org/10.1039/d0ra01348j.
Повний текст джерелаAl-Hazam, Hanan A., Zeki A. Al-Shamkani, Najim A. Al-Masoudi, Bahjat A. Saeed, and Christophe Pannecouque. "New chalcones and thiopyrimidine analogues derived from mefenamic acid: microwave-assisted synthesis, anti-HIV activity and cytotoxicity as antileukemic agents." Zeitschrift für Naturforschung B 72, no. 4 (April 1, 2017): 249–56. http://dx.doi.org/10.1515/znb-2016-0223.
Повний текст джерелаMoir, Michael, Rochelle Boyd, Hendra Gunosewoyo, Andrew P. Montgomery, Mark Connor, and Michael Kassiou. "Synthesis and evaluation of various heteroaromatic benzamides as analogues of –ylidene-benzamide cannabinoid type 2 receptor agonists." Tetrahedron Letters 60, no. 36 (September 2019): 151019. http://dx.doi.org/10.1016/j.tetlet.2019.151019.
Повний текст джерелаTu, Zhude, Jinbin Xu, Lynne A. Jones, Shihong Li, Craig Dumstorff, Suwanna Vangveravong, Delphine L. Chen, Kenneth T. Wheeler, Michael J. Welch та Robert H. Mach. "Fluorine-18-Labeled Benzamide Analogues for Imaging the σ2Receptor Status of Solid Tumors with Positron Emission Tomography". Journal of Medicinal Chemistry 50, № 14 (липень 2007): 3194–204. http://dx.doi.org/10.1021/jm0614883.
Повний текст джерелаDiouf, O., M. Bourhim, D. M. Lambert, J. H. Poupaert, J. P. Stables, and J. Vamecq. "Anticonvulsant and neurotoxicological properties of 4-amino-N-(2-ethylphenyl)benzamide, a potent ameltolide analogue." Biomedicine & Pharmacotherapy 51, no. 3 (January 1997): 131–36. http://dx.doi.org/10.1016/s0753-3322(97)86911-9.
Повний текст джерелаGradillas, Ana, Berta López, Miguel Braña, Isabel Sancho, Carmen Pérez-García, and Luis Alguacil. "Synthesis and Biological Activity of Picobenzide (3,5-Dimethyl-N-(pyridin-4-ylmethyl)benzamide) Analogues as Potential Antipsychotic Agents." Arzneimittelforschung 55, no. 12 (December 23, 2011): 725–29. http://dx.doi.org/10.1055/s-0031-1296921.
Повний текст джерелаHalton, Brian, Carissa S. Jones, Peter T. Northcote, and Roland Boese. "Studies in the Cycloproparene Series: Formation of a New Dimer of 1H-Cyclopropa[b]naphthalene." Australian Journal of Chemistry 52, no. 4 (1999): 285. http://dx.doi.org/10.1071/c98179.
Повний текст джерелаTripathy, Swayansiddha, Mohammed Afzal Azam, Srikanth Jupudi, and Susanta Kumar Sahu. "Pharmacophore generation, atom-based 3D-QSAR, molecular docking and molecular dynamics simulation studies on benzamide analogues as FtsZ inhibitors." Journal of Biomolecular Structure and Dynamics 36, no. 12 (October 11, 2017): 3218–30. http://dx.doi.org/10.1080/07391102.2017.1384401.
Повний текст джерелаBai, Suping, Shihong Li, Jinbin Xu, Xin Peng, Kiran Sai, Wenhua Chu, Zhude Tu, Chenbo Zeng та Robert H. Mach. "Synthesis and Structure–Activity Relationship Studies of Conformationally Flexible Tetrahydroisoquinolinyl Triazole Carboxamide and Triazole Substituted Benzamide Analogues as σ2 Receptor Ligands". Journal of Medicinal Chemistry 57, № 10 (12 травня 2014): 4239–51. http://dx.doi.org/10.1021/jm5001453.
Повний текст джерелаGrewal, Ajmer Singh, Rajeev Kharb, Deo Nandan Prasad, Jagdeep Singh Dua, and Viney Lather. "N-pyridin-2-yl benzamide analogues as allosteric activators of glucokinase: Design, synthesis, in vitro,in silico and in vivo evaluation." Chemical Biology & Drug Design 93, no. 3 (November 28, 2018): 364–72. http://dx.doi.org/10.1111/cbdd.13423.
Повний текст джерелаSagar, Belakavadi K., Hemmige S. Yathirajan, Ravindranath S. Rathore, and Christopher Glidewell. "Four closely related N-(3-benzoyl-4,5,6,7-tetrahydrobenzo[b]thiophen-2-yl)benzamides: order versus disorder, and similar molecular conformations but different modes of supramolecular aggregation, with a new disordered refinement of 2-amino-3-benzoyl-4,5,6,7-tetrahydrobenzo[b]thiophene." Acta Crystallographica Section C Structural Chemistry 74, no. 1 (January 1, 2018): 45–53. http://dx.doi.org/10.1107/s2053229617017326.
Повний текст джерелаИванова, E. Ivanova, Мелешкин, A. Meleshkin, Скачилова, S. Skachilova, Елизарова, et al. "A Comparative Study of Toxicity and the Scale of Activity of New N-Substituted Benzamide Derivative." Journal of New Medical Technologies 22, no. 1 (February 11, 2015): 16–19. http://dx.doi.org/10.12737/9069.
Повний текст джерелаCampkin, David M., Yuna Shimadate, Barbara Bartholomew, Paul V. Bernhardt, Robert J. Nash, Jennette A. Sakoff, Atsushi Kato, and Michela I. Simone. "Borylated 2,3,4,5-Tetrachlorophthalimide and Their 2,3,4,5-Tetrachlorobenzamide Analogues: Synthesis, Their Glycosidase Inhibition and Anticancer Properties in View to Boron Neutron Capture Therapy." Molecules 27, no. 11 (May 26, 2022): 3447. http://dx.doi.org/10.3390/molecules27113447.
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