Статті в журналах з теми "Triazole isosters"
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Franco, Daiana Portella, Lucas Caruso, Nathalia Fonseca Nadur, Thiago Moreira Pereira, Renata Barbosa Lacerda, and Arthur Eugen Kümmerle. "Recent Advances in Microwave-Assisted Synthesis and Functionalization of 1,2,3- and 1,2,4-triazoles." Current Organic Chemistry 25, no. 23 (December 16, 2021): 2815–39. http://dx.doi.org/10.2174/1385272825666211011111408.
Повний текст джерелаSahu, Adarsh, Preeti Sahu, and Ramkishore Agrawal. "A Recent Review on Drug Modification Using 1,2,3-triazole." Current Chemical Biology 14, no. 2 (November 19, 2020): 71–87. http://dx.doi.org/10.2174/2212796814999200807214519.
Повний текст джерелаPanja, Atanu, and Kumaresh Ghosh. "Triazole-amide isosteric pyridine-based supramolecular gelators in metal ion and biothiol sensing with excellent performance in adsorption of heavy metal ions and picric acid from water." New Journal of Chemistry 43, no. 2 (2019): 934–45. http://dx.doi.org/10.1039/c8nj04380a.
Повний текст джерелаAlagodla, Ramesh, Paturu Rama Subba Reddy, Sravanthi Vemireddy, Devdutt Chaturvedi, and Halmuthur M. Sampath Kumar. "Synthesis of Novel 1,2,3-Triazolyl L-Serinol Palmitoyl Muramyl Dipeptide Derivatives." Asian Journal of Chemistry 35, no. 3 (2023): 763–70. http://dx.doi.org/10.14233/ajchem.2023.27553.
Повний текст джерелаWu, Jun, Nikolaos Kaplaneris, Shaofei Ni, Felix Kaltenhäuser, and Lutz Ackermann. "Late-stage C(sp2)–H and C(sp3)–H glycosylation of C-aryl/alkyl glycopeptides: mechanistic insights and fluorescence labeling." Chemical Science 11, no. 25 (2020): 6521–26. http://dx.doi.org/10.1039/d0sc01260b.
Повний текст джерелаRečnik, Lisa-Maria, Wolfgang Kandioller, and Thomas L. Mindt. "1,4-Disubstituted 1,2,3-Triazoles as Amide Bond Surrogates for the Stabilisation of Linear Peptides with Biological Activity." Molecules 25, no. 16 (August 6, 2020): 3576. http://dx.doi.org/10.3390/molecules25163576.
Повний текст джерелаWales, Steven M., Katherine A. Hammer, Amy M. King, Andrew J. Tague, Dena Lyras, Thomas V. Riley, Paul A. Keller, and Stephen G. Pyne. "Binaphthyl-1,2,3-triazole peptidomimetics with activity against Clostridium difficile and other pathogenic bacteria." Organic & Biomolecular Chemistry 13, no. 20 (2015): 5743–56. http://dx.doi.org/10.1039/c5ob00576k.
Повний текст джерелаTautz, Markus, Juan Torras, Santiago Grijalvo, Ramón Eritja, César Saldías, Carlos Alemán, and David Díaz Díaz. "Expanding the limits of amide–triazole isosteric substitution in bisamide-based physical gels." RSC Advances 9, no. 36 (2019): 20841–51. http://dx.doi.org/10.1039/c9ra03316e.
Повний текст джерелаTautz, Markus, César Saldías, Antonio Diego Lozano-Gorrín, and David Díaz Díaz. "Use of a bis-1,2,3-triazole gelator for the preparation of supramolecular metallogels and stabilization of gold nanoparticles." New Journal of Chemistry 43, no. 35 (2019): 13850–56. http://dx.doi.org/10.1039/c9nj03427g.
Повний текст джерелаJunaid, Lim, Zhou, Chui, and Dolzhenko. "Fused Heterocyclic Systems with an s-Triazine Ring. 34. Development of a Practical Approach for the Synthesis of 5-Aza-isoguanines." Molecules 24, no. 8 (April 12, 2019): 1453. http://dx.doi.org/10.3390/molecules24081453.
Повний текст джерелаRani, Alisha, Gurjaspreet Singh, Akshpreet Singh, Ubair Maqbool, Gurpreet Kaur, and Jandeep Singh. "CuAAC-ensembled 1,2,3-triazole-linked isosteres as pharmacophores in drug discovery: review." RSC Advances 10, no. 10 (2020): 5610–35. http://dx.doi.org/10.1039/c9ra09510a.
Повний текст джерелаRjabovs, Vitālijs, Pāvels Ostrovskis, Daniels Posevins, Gļebs Kiseļovs, Viktors Kumpiņš, Anatoly Mishnev, and Māris Turks. "Synthesis of Building Blocks for Carbopeptoids and Their Triazole Isoster Assembly." European Journal of Organic Chemistry 2015, no. 25 (July 23, 2015): 5572–84. http://dx.doi.org/10.1002/ejoc.201500695.
Повний текст джерелаBachl, Jürgen, Judith Mayr, Francisco J. Sayago, Carlos Cativiela, and David Díaz Díaz. "Amide–triazole isosteric substitution for tuning self-assembly and incorporating new functions into soft supramolecular materials." Chemical Communications 51, no. 25 (2015): 5294–97. http://dx.doi.org/10.1039/c4cc08593k.
Повний текст джерелаRep, Valentina, Martina Piškor, Helena Šimek, Petra Mišetić, Petra Grbčić, Jasna Padovan, Vesna Gabelica Marković, et al. "Purine and Purine Isostere Derivatives of Ferrocene: An Evaluation of ADME, Antitumor and Electrochemical Properties." Molecules 25, no. 7 (March 29, 2020): 1570. http://dx.doi.org/10.3390/molecules25071570.
Повний текст джерелаBock, Victoria D., Dave Speijer, Henk Hiemstra, and Jan H. van Maarseveen. "1,2,3-Triazoles as peptide bond isosteres: synthesis and biological evaluation of cyclotetrapeptide mimics." Organic & Biomolecular Chemistry 5, no. 6 (2007): 971. http://dx.doi.org/10.1039/b616751a.
Повний текст джерелаHäring, Marleen, Julio Rodríguez-López, Santiago Grijalvo, Markus Tautz, Ramón Eritja, Víctor S. Martín, and David Díaz Díaz. "Isosteric Substitution of 4H-1,2,4-Triazole by 1H-1,2,3-Triazole in Isophthalic Derivative Enabled Hydrogel Formation for Controlled Drug Delivery." Molecular Pharmaceutics 15, no. 8 (February 15, 2018): 2963–72. http://dx.doi.org/10.1021/acs.molpharmaceut.7b01049.
Повний текст джерелаGrob, Nathalie M., Roger Schibli, Martin Béhé, Ibai E. Valverde, and Thomas L. Mindt. "1,5-Disubstituted 1,2,3-Triazoles as Amide Bond Isosteres Yield Novel Tumor-Targeting Minigastrin Analogs." ACS Medicinal Chemistry Letters 12, no. 4 (March 16, 2021): 585–92. http://dx.doi.org/10.1021/acsmedchemlett.0c00636.
Повний текст джерелаSahu, Adarsh, Debashree Das, Ram Kishore Agrawal, and Asmita Gajbhiye. "Bio-isosteric replacement of amide group with 1,2,3-triazole in phenacetin improves the toxicology and efficacy of phenacetin-triazole conjugates (PhTCs)." Life Sciences 228 (July 2019): 176–88. http://dx.doi.org/10.1016/j.lfs.2019.05.004.
Повний текст джерелаZálešák, František, Jan Slouka, and Jakub Stýskala. "General Synthesis of 1-Aryl-6-azaisocytosines and Their Utilization for the Preparation of Related Condensed 1,2,4-Triazines." Molecules 24, no. 19 (October 1, 2019): 3558. http://dx.doi.org/10.3390/molecules24193558.
Повний текст джерелаCorredor, Miriam, Jordi Bujons, Mar Orzáez, Mónica Sancho, Enrique Pérez-Payá, Ignacio Alfonso, and Angel Messeguer. "Optimizing the control of apoptosis by amide/triazole isosteric substitution in a constrained peptoid." European Journal of Medicinal Chemistry 63 (May 2013): 892–96. http://dx.doi.org/10.1016/j.ejmech.2013.03.004.
Повний текст джерелаShultz, Michael D., Dyuti Majumdar, Donovan N. Chin, Pascal D. Fortin, Yun Feng, Ty Gould, Christina A. Kirby, Travis Stams, Nigel J. Waters, and Wenlin Shao. "Structure–Efficiency Relationship of [1,2,4]Triazol-3-ylamines as Novel Nicotinamide Isosteres that Inhibit Tankyrases." Journal of Medicinal Chemistry 56, no. 17 (August 14, 2013): 7049–59. http://dx.doi.org/10.1021/jm400826j.
Повний текст джерелаKaras, John, Fazel Shabanpoor, Mohammed Akhter Hossain, James Gardiner, Frances Separovic, John D. Wade, and Denis B. Scanlon. "Total Chemical Synthesis of a Heterodimeric Interchain Bis-Lactam-Linked Peptide: Application to an Analogue of Human Insulin-Like Peptide 3." International Journal of Peptides 2013 (October 28, 2013): 1–8. http://dx.doi.org/10.1155/2013/504260.
Повний текст джерелаZavodskaya, Anna V., Vladimir V. Bakharev, Victor E. Parfenov, Alexander A. Gidaspov, Pavel A. Slepukhin, Maksim L. Isenov, and Oleg S. Eltsov. "Synthesis of new 5-aza-isosteres of guanine containing aryl and hetaryl substituents on the 1,2,4-triazole ring." Tetrahedron Letters 56, no. 9 (February 2015): 1103–6. http://dx.doi.org/10.1016/j.tetlet.2015.01.151.
Повний текст джерелаMonceaux, Christopher J., Chiho Hirata-Fukae, Polo C. H. Lam, Maxim M. Totrov, Yasuji Matsuoka, and Paul R. Carlier. "Triazole-linked reduced amide isosteres: An approach for the fragment-based drug discovery of anti-Alzheimer’s BACE1 inhibitors." Bioorganic & Medicinal Chemistry Letters 21, no. 13 (July 2011): 3992–96. http://dx.doi.org/10.1016/j.bmcl.2011.05.007.
Повний текст джерелаLim, Felicia Phei Lin, and Anton V. Dolzhenko. "1,3,5-Triazine-based analogues of purine: From isosteres to privileged scaffolds in medicinal chemistry." European Journal of Medicinal Chemistry 85 (October 2014): 371–90. http://dx.doi.org/10.1016/j.ejmech.2014.07.112.
Повний текст джерелаNishimura, Natsu, Ai Kato, and Isamu Maeba. "Synthesis of pyrrolo[2,1-f][1,2,4]triazine C-nucleosides. Isosteres of sangivamycin, tubercidin, and toyocamycin." Carbohydrate Research 331, no. 1 (March 2001): 77–82. http://dx.doi.org/10.1016/s0008-6215(01)00017-9.
Повний текст джерелаZhang, Jian-Wei, Man-Cheng Hu, Shu-Ni Li, Yu-Cheng Jiang, and Quan-Guo Zhai. "Microporous rod metal–organic frameworks with diverse Zn/Cd–triazolate ribbons as secondary building units for CO2 uptake and selective adsorption of hydrocarbons." Dalton Transactions 46, no. 3 (2017): 836–44. http://dx.doi.org/10.1039/c6dt04433f.
Повний текст джерелаBakharev, Vladimir V., Victor E. Parfenov, Irina V. Ul'yankina, Anna V. Zavodskaya, Evgeniya V. Selezneva, Alexander A. Gidaspov, Oleg S. Eltsov, and Pavel A. Slepukhin. "Synthesis of new 5-aza-isosteres of guanine—5-aminosubstituted 1,2,4-triazolo[1,5-a]-1,3,5-triazin-7-ones." Tetrahedron 70, no. 38 (September 2014): 6825–30. http://dx.doi.org/10.1016/j.tet.2014.07.058.
Повний текст джерелаLim, Felicia Phei Lin, and Anton V. Dolzhenko. "ChemInform Abstract: 1,3,5-Triazine-Based Analogues of Purine: From Isosteres to Privileged Scaffolds in Medicinal Chemistry." ChemInform 45, no. 45 (October 23, 2014): no. http://dx.doi.org/10.1002/chin.201445288.
Повний текст джерелаChopra, Pratiksha N., and Jagdish K. Sahu. "Biological Significance of Imidazole-based Analogues in New Drug Development." Current Drug Discovery Technologies 17, no. 5 (December 23, 2020): 574–84. http://dx.doi.org/10.2174/1570163816666190320123340.
Повний текст джерелаBauer, Michaela, Wei Wang, Mélanie M. Lorion, Chuan Dong, and Lutz Ackermann. "Internal Peptide Late-Stage Diversification: Peptide-Isosteric Triazoles for Primary and Secondary C(sp3 )−H Activation." Angewandte Chemie International Edition 57, no. 1 (December 5, 2017): 203–7. http://dx.doi.org/10.1002/anie.201710136.
Повний текст джерелаBauer, Michaela, Wei Wang, Mélanie M. Lorion, Chuan Dong, and Lutz Ackermann. "Internal Peptide Late-Stage Diversification: Peptide-Isosteric Triazoles for Primary and Secondary C(sp3 )−H Activation." Angewandte Chemie 130, no. 1 (December 5, 2017): 209–13. http://dx.doi.org/10.1002/ange.201710136.
Повний текст джерелаPerissutti, Elisa, Francesco Frecentese, Ferdinando Fiorino, Beatrice Severino, Donatella Cirillo, Vincenzo Santagada, and Giuseppe Caliendo. "Microwave solvent free regioselective 1,3 dipolar cycloaddition in the synthesis of 1,4 substituted [1,2,3]-triazoles as amide bond isosteres." Journal of Heterocyclic Chemistry 44, no. 4 (July 2007): 815–19. http://dx.doi.org/10.1002/jhet.5570440410.
Повний текст джерелаNishimura, Natsu, Ai Kato, and Isamu Maeba. "ChemInform Abstract: Synthesis of Pyrrolo[2,1-f][1,2,4]triazine C-Nucleosides. Isosteres of Sangivamycin, Tubercidin, and Toyocamycin." ChemInform 32, no. 26 (May 25, 2010): no. http://dx.doi.org/10.1002/chin.200126214.
Повний текст джерелаFedorczyk, Bartlomiej, Piotr F. J. Lipiński, Anna K. Puszko, Dagmara Tymecka, Beata Wilenska, Wioleta Dudka, Gerard Y. Perret, Rafal Wieczorek, and Aleksandra Misicka. "Triazolopeptides Inhibiting the Interaction between Neuropilin-1 and Vascular Endothelial Growth Factor-165." Molecules 24, no. 9 (May 6, 2019): 1756. http://dx.doi.org/10.3390/molecules24091756.
Повний текст джерелаCaulkett, Peter W. R., Geraint Jones, Mary McPartlin, Nigel D. Renshaw, Sarah K. Stewart, and Brian Wright. "Adenine isosteres with bridgehead nitrogen. Part 1. Two independent syntheses of the [1,2,4]triazolo[1,5-a][1,3,5]triazine ring system leading to a range of substituents in the 2, 5 and 7 positions." Journal of the Chemical Society, Perkin Transactions 1, no. 7 (1995): 801. http://dx.doi.org/10.1039/p19950000801.
Повний текст джерелаIvanenkov, Yan A., Renat S. Yamidanov, Ilya A. Osterman, Petr V. Sergiev, Vladimir A. Aladinskiy, Anastasia V. Aladinskaya, Victor A. Terentiev, et al. "Identification of N-Substituted Triazolo-azetidines as Novel Antibacterials using pDualrep2 HTS Platform." Combinatorial Chemistry & High Throughput Screening 22, no. 5 (August 8, 2019): 346–54. http://dx.doi.org/10.2174/1386207322666190412165316.
Повний текст джерелаBakharev, Vladimir V., Victor E. Parfenov, Irina V. Ul'yankina, Anna V. Zavodskaya, Evgeniya V. Selezneva, Alexander A. Gidaspov, Oleg S. Eltsov, and Pavel A. Slepukhin. "ChemInform Abstract: Synthesis of New 5-Aza-isosteres of Guanine-5-Aminosubstituted 1,2,4-Triazolo[1,5-a]-1,3,5-triazin-7-ones." ChemInform 46, no. 6 (January 23, 2015): no. http://dx.doi.org/10.1002/chin.201506175.
Повний текст джерелаOstrowski, T., and J. Zeidler. "Synthesis of 5-ethynyl-1- -D-ribofuranosyl-1H-[1,2,3]triazole-4-carboxylic acid amide (isosteric to EICAR) and its derivatives." Nucleic Acids Symposium Series 52, no. 1 (September 1, 2008): 585–86. http://dx.doi.org/10.1093/nass/nrn296.
Повний текст джерелаCAULKETT, P. W. R., G. JONES, M. MCPARTLIN, N. D. RENSHAW, S. K. STEWART, and B. WRIGHT. "ChemInform Abstract: Adenine Isosteres with Bridgehead Nitrogen. Part 1. Two Independent Syntheses of the (1,2,4)Triazolo(1,5-a)(1,3,5)triazine Ring System Leading to a Range of Substituents in the 2, 5 and 7 Positions." ChemInform 26, no. 34 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199534183.
Повний текст джерелаBradbury, Robert H., John S. Major, Alec A. Oldham, Janet E. Rivett, David A. Roberts, Anthony M. Slater, David Timms, and David Waterson. "1,2,4-Triazolo[4,3-a]pyrazine derivatives with human renin inhibitory activity. 2. Synthesis, biological properties and molecular modeling of hydroxyethylene isostere derivatives." Journal of Medicinal Chemistry 33, no. 9 (September 1990): 2335–42. http://dx.doi.org/10.1021/jm00171a006.
Повний текст джерелаSampognaro, Anthony J., Mark D. Wittman, Joan M. Carboni, Chiehying Chang, Ann F. Greer, Warren W. Hurlburt, John S. Sack, and Dolatrai M. Vyas. "Proline isosteres in a series of 2,4-disubstituted pyrrolo[1,2-f][1,2,4]triazine inhibitors of IGF-1R kinase and IR kinase." Bioorganic & Medicinal Chemistry Letters 20, no. 17 (September 2010): 5027–30. http://dx.doi.org/10.1016/j.bmcl.2010.07.045.
Повний текст джерелаBRADBURY, R. H., J. S. MAJOR, A. A. OLDHAM, J. E. RIVETT, D. A. ROBERTS, A. M. SLATER, D. TIMMS, and D. WATERSON. "ChemInform Abstract: 1,2,4-Triazolo(4,3-a)pyrazine Derivatives with Human Renin Inhibitory Activity. Part 2. Synthesis, Biological Properties, and Molecular Modeling of Hydroxyethylene Isostere Derivatives." ChemInform 22, no. 8 (August 23, 2010): no. http://dx.doi.org/10.1002/chin.199108220.
Повний текст джерелаFocken, Thilo, Sultan Chowdhury, Alla Zenova, Michael E. Grimwood, Christine Chabot, Tao Sheng, Ivan Hemeon, et al. "Design of Conformationally Constrained Acyl Sulfonamide Isosteres: Identification of N-([1,2,4]Triazolo[4,3-a]pyridin-3-yl)methane-sulfonamides as Potent and Selective hNaV1.7 Inhibitors for the Treatment of Pain." Journal of Medicinal Chemistry 61, no. 11 (May 8, 2018): 4810–31. http://dx.doi.org/10.1021/acs.jmedchem.7b01826.
Повний текст джерелаRoma, Giorgio, Giancarlo Grossi, Mario Di Braccio, Daniela Piras, Vigilio Ballabeni, Massimiliano Tognolini, Simona Bertoni, and Elisabetta Barocelli. "1,8-Naphthyridines VII. New substituted 5-amino[1,2,4]triazolo[4,3-a][1,8]naphthyridine-6-carboxamides and their isosteric analogues, exhibiting notable anti-inflammatory and/or analgesic activities, but no acute gastrolesivity." European Journal of Medicinal Chemistry 43, no. 8 (August 2008): 1665–80. http://dx.doi.org/10.1016/j.ejmech.2007.10.010.
Повний текст джерелаKumar, Sachin, Sukhbir Lal Khokra, and Akash Yadav. "Triazole analogues as potential pharmacological agents: a brief review." Future Journal of Pharmaceutical Sciences 7, no. 1 (May 25, 2021). http://dx.doi.org/10.1186/s43094-021-00241-3.
Повний текст джерелаLal, Kashmiri, Aman Kumar, Yajat Rohila, and Vijay Kumar. "A Mini Review on Pharmacological Significance of Isatin-1,2,3-Triazole Hybrids." Current Topics in Medicinal Chemistry 23 (February 2, 2023). http://dx.doi.org/10.2174/1568026623666230202160925.
Повний текст джерелаPerissutti, Elisa, Francesco Frecentese, Ferdinando Fiorino, Beatrice Severino, Donatella Cirillo, Vincenzo Santagada, and Giuseppe Caliendo. "Microwave Solvent-Free Regioselective 1,3-Dipolar Cycloaddition in the Synthesis of 1,4-Substituted[1,2,3]-triazoles as Amide Bond Isosteres." ChemInform 38, no. 47 (November 20, 2007). http://dx.doi.org/10.1002/chin.200747133.
Повний текст джерела"Synthesis and Cytotoxic Activity of New Pyrimido[1,2-c]quinazolines, [1,2,4]triazolo[4,3-c]quinazolines and (quinazolin-4-yl)-1H-pyrazoles Hybrids." Biointerface Research in Applied Chemistry 12, no. 4 (October 17, 2021): 5217–33. http://dx.doi.org/10.33263/briac124.52175233.
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