Artículos de revistas sobre el tema "Triazole isosters"
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Franco, Daiana Portella, Lucas Caruso, Nathalia Fonseca Nadur, Thiago Moreira Pereira, Renata Barbosa Lacerda y Arthur Eugen Kümmerle. "Recent Advances in Microwave-Assisted Synthesis and Functionalization of 1,2,3- and 1,2,4-triazoles". Current Organic Chemistry 25, n.º 23 (16 de diciembre de 2021): 2815–39. http://dx.doi.org/10.2174/1385272825666211011111408.
Texto completoSahu, Adarsh, Preeti Sahu y Ramkishore Agrawal. "A Recent Review on Drug Modification Using 1,2,3-triazole". Current Chemical Biology 14, n.º 2 (19 de noviembre de 2020): 71–87. http://dx.doi.org/10.2174/2212796814999200807214519.
Texto completoPanja, Atanu y 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, n.º 2 (2019): 934–45. http://dx.doi.org/10.1039/c8nj04380a.
Texto completoAlagodla, Ramesh, Paturu Rama Subba Reddy, Sravanthi Vemireddy, Devdutt Chaturvedi y Halmuthur M. Sampath Kumar. "Synthesis of Novel 1,2,3-Triazolyl L-Serinol Palmitoyl Muramyl Dipeptide Derivatives". Asian Journal of Chemistry 35, n.º 3 (2023): 763–70. http://dx.doi.org/10.14233/ajchem.2023.27553.
Texto completoWu, Jun, Nikolaos Kaplaneris, Shaofei Ni, Felix Kaltenhäuser y 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, n.º 25 (2020): 6521–26. http://dx.doi.org/10.1039/d0sc01260b.
Texto completoRečnik, Lisa-Maria, Wolfgang Kandioller y 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, n.º 16 (6 de agosto de 2020): 3576. http://dx.doi.org/10.3390/molecules25163576.
Texto completoWales, Steven M., Katherine A. Hammer, Amy M. King, Andrew J. Tague, Dena Lyras, Thomas V. Riley, Paul A. Keller y Stephen G. Pyne. "Binaphthyl-1,2,3-triazole peptidomimetics with activity against Clostridium difficile and other pathogenic bacteria". Organic & Biomolecular Chemistry 13, n.º 20 (2015): 5743–56. http://dx.doi.org/10.1039/c5ob00576k.
Texto completoTautz, Markus, Juan Torras, Santiago Grijalvo, Ramón Eritja, César Saldías, Carlos Alemán y David Díaz Díaz. "Expanding the limits of amide–triazole isosteric substitution in bisamide-based physical gels". RSC Advances 9, n.º 36 (2019): 20841–51. http://dx.doi.org/10.1039/c9ra03316e.
Texto completoTautz, Markus, César Saldías, Antonio Diego Lozano-Gorrín y 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, n.º 35 (2019): 13850–56. http://dx.doi.org/10.1039/c9nj03427g.
Texto completoJunaid, Lim, Zhou, Chui y Dolzhenko. "Fused Heterocyclic Systems with an s-Triazine Ring. 34. Development of a Practical Approach for the Synthesis of 5-Aza-isoguanines". Molecules 24, n.º 8 (12 de abril de 2019): 1453. http://dx.doi.org/10.3390/molecules24081453.
Texto completoRani, Alisha, Gurjaspreet Singh, Akshpreet Singh, Ubair Maqbool, Gurpreet Kaur y Jandeep Singh. "CuAAC-ensembled 1,2,3-triazole-linked isosteres as pharmacophores in drug discovery: review". RSC Advances 10, n.º 10 (2020): 5610–35. http://dx.doi.org/10.1039/c9ra09510a.
Texto completoRjabovs, Vitālijs, Pāvels Ostrovskis, Daniels Posevins, Gļebs Kiseļovs, Viktors Kumpiņš, Anatoly Mishnev y Māris Turks. "Synthesis of Building Blocks for Carbopeptoids and Their Triazole Isoster Assembly". European Journal of Organic Chemistry 2015, n.º 25 (23 de julio de 2015): 5572–84. http://dx.doi.org/10.1002/ejoc.201500695.
Texto completoBachl, Jürgen, Judith Mayr, Francisco J. Sayago, Carlos Cativiela y David Díaz Díaz. "Amide–triazole isosteric substitution for tuning self-assembly and incorporating new functions into soft supramolecular materials". Chemical Communications 51, n.º 25 (2015): 5294–97. http://dx.doi.org/10.1039/c4cc08593k.
Texto completoRep, 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, n.º 7 (29 de marzo de 2020): 1570. http://dx.doi.org/10.3390/molecules25071570.
Texto completoBock, Victoria D., Dave Speijer, Henk Hiemstra y Jan H. van Maarseveen. "1,2,3-Triazoles as peptide bond isosteres: synthesis and biological evaluation of cyclotetrapeptide mimics". Organic & Biomolecular Chemistry 5, n.º 6 (2007): 971. http://dx.doi.org/10.1039/b616751a.
Texto completoHäring, Marleen, Julio Rodríguez-López, Santiago Grijalvo, Markus Tautz, Ramón Eritja, Víctor S. Martín y 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, n.º 8 (15 de febrero de 2018): 2963–72. http://dx.doi.org/10.1021/acs.molpharmaceut.7b01049.
Texto completoGrob, Nathalie M., Roger Schibli, Martin Béhé, Ibai E. Valverde y 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, n.º 4 (16 de marzo de 2021): 585–92. http://dx.doi.org/10.1021/acsmedchemlett.0c00636.
Texto completoSahu, Adarsh, Debashree Das, Ram Kishore Agrawal y 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 (julio de 2019): 176–88. http://dx.doi.org/10.1016/j.lfs.2019.05.004.
Texto completoZálešák, František, Jan Slouka y Jakub Stýskala. "General Synthesis of 1-Aryl-6-azaisocytosines and Their Utilization for the Preparation of Related Condensed 1,2,4-Triazines". Molecules 24, n.º 19 (1 de octubre de 2019): 3558. http://dx.doi.org/10.3390/molecules24193558.
Texto completoCorredor, Miriam, Jordi Bujons, Mar Orzáez, Mónica Sancho, Enrique Pérez-Payá, Ignacio Alfonso y Angel Messeguer. "Optimizing the control of apoptosis by amide/triazole isosteric substitution in a constrained peptoid". European Journal of Medicinal Chemistry 63 (mayo de 2013): 892–96. http://dx.doi.org/10.1016/j.ejmech.2013.03.004.
Texto completoShultz, Michael D., Dyuti Majumdar, Donovan N. Chin, Pascal D. Fortin, Yun Feng, Ty Gould, Christina A. Kirby, Travis Stams, Nigel J. Waters y Wenlin Shao. "Structure–Efficiency Relationship of [1,2,4]Triazol-3-ylamines as Novel Nicotinamide Isosteres that Inhibit Tankyrases". Journal of Medicinal Chemistry 56, n.º 17 (14 de agosto de 2013): 7049–59. http://dx.doi.org/10.1021/jm400826j.
Texto completoKaras, John, Fazel Shabanpoor, Mohammed Akhter Hossain, James Gardiner, Frances Separovic, John D. Wade y 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 (28 de octubre de 2013): 1–8. http://dx.doi.org/10.1155/2013/504260.
Texto completoZavodskaya, Anna V., Vladimir V. Bakharev, Victor E. Parfenov, Alexander A. Gidaspov, Pavel A. Slepukhin, Maksim L. Isenov y 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, n.º 9 (febrero de 2015): 1103–6. http://dx.doi.org/10.1016/j.tetlet.2015.01.151.
Texto completoMonceaux, Christopher J., Chiho Hirata-Fukae, Polo C. H. Lam, Maxim M. Totrov, Yasuji Matsuoka y 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, n.º 13 (julio de 2011): 3992–96. http://dx.doi.org/10.1016/j.bmcl.2011.05.007.
Texto completoLim, Felicia Phei Lin y 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 (octubre de 2014): 371–90. http://dx.doi.org/10.1016/j.ejmech.2014.07.112.
Texto completoNishimura, Natsu, Ai Kato y Isamu Maeba. "Synthesis of pyrrolo[2,1-f][1,2,4]triazine C-nucleosides. Isosteres of sangivamycin, tubercidin, and toyocamycin". Carbohydrate Research 331, n.º 1 (marzo de 2001): 77–82. http://dx.doi.org/10.1016/s0008-6215(01)00017-9.
Texto completoZhang, Jian-Wei, Man-Cheng Hu, Shu-Ni Li, Yu-Cheng Jiang y 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, n.º 3 (2017): 836–44. http://dx.doi.org/10.1039/c6dt04433f.
Texto completoBakharev, Vladimir V., Victor E. Parfenov, Irina V. Ul'yankina, Anna V. Zavodskaya, Evgeniya V. Selezneva, Alexander A. Gidaspov, Oleg S. Eltsov y 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, n.º 38 (septiembre de 2014): 6825–30. http://dx.doi.org/10.1016/j.tet.2014.07.058.
Texto completoLim, Felicia Phei Lin y Anton V. Dolzhenko. "ChemInform Abstract: 1,3,5-Triazine-Based Analogues of Purine: From Isosteres to Privileged Scaffolds in Medicinal Chemistry". ChemInform 45, n.º 45 (23 de octubre de 2014): no. http://dx.doi.org/10.1002/chin.201445288.
Texto completoChopra, Pratiksha N. y Jagdish K. Sahu. "Biological Significance of Imidazole-based Analogues in New Drug Development". Current Drug Discovery Technologies 17, n.º 5 (23 de diciembre de 2020): 574–84. http://dx.doi.org/10.2174/1570163816666190320123340.
Texto completoBauer, Michaela, Wei Wang, Mélanie M. Lorion, Chuan Dong y Lutz Ackermann. "Internal Peptide Late-Stage Diversification: Peptide-Isosteric Triazoles for Primary and Secondary C(sp3 )−H Activation". Angewandte Chemie International Edition 57, n.º 1 (5 de diciembre de 2017): 203–7. http://dx.doi.org/10.1002/anie.201710136.
Texto completoBauer, Michaela, Wei Wang, Mélanie M. Lorion, Chuan Dong y Lutz Ackermann. "Internal Peptide Late-Stage Diversification: Peptide-Isosteric Triazoles for Primary and Secondary C(sp3 )−H Activation". Angewandte Chemie 130, n.º 1 (5 de diciembre de 2017): 209–13. http://dx.doi.org/10.1002/ange.201710136.
Texto completoPerissutti, Elisa, Francesco Frecentese, Ferdinando Fiorino, Beatrice Severino, Donatella Cirillo, Vincenzo Santagada y 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, n.º 4 (julio de 2007): 815–19. http://dx.doi.org/10.1002/jhet.5570440410.
Texto completoNishimura, Natsu, Ai Kato y Isamu Maeba. "ChemInform Abstract: Synthesis of Pyrrolo[2,1-f][1,2,4]triazine C-Nucleosides. Isosteres of Sangivamycin, Tubercidin, and Toyocamycin." ChemInform 32, n.º 26 (25 de mayo de 2010): no. http://dx.doi.org/10.1002/chin.200126214.
Texto completoFedorczyk, Bartlomiej, Piotr F. J. Lipiński, Anna K. Puszko, Dagmara Tymecka, Beata Wilenska, Wioleta Dudka, Gerard Y. Perret, Rafal Wieczorek y Aleksandra Misicka. "Triazolopeptides Inhibiting the Interaction between Neuropilin-1 and Vascular Endothelial Growth Factor-165". Molecules 24, n.º 9 (6 de mayo de 2019): 1756. http://dx.doi.org/10.3390/molecules24091756.
Texto completoCaulkett, Peter W. R., Geraint Jones, Mary McPartlin, Nigel D. Renshaw, Sarah K. Stewart y 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, n.º 7 (1995): 801. http://dx.doi.org/10.1039/p19950000801.
Texto completoIvanenkov, 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, n.º 5 (8 de agosto de 2019): 346–54. http://dx.doi.org/10.2174/1386207322666190412165316.
Texto completoBakharev, Vladimir V., Victor E. Parfenov, Irina V. Ul'yankina, Anna V. Zavodskaya, Evgeniya V. Selezneva, Alexander A. Gidaspov, Oleg S. Eltsov y 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, n.º 6 (23 de enero de 2015): no. http://dx.doi.org/10.1002/chin.201506175.
Texto completoOstrowski, T. y 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, n.º 1 (1 de septiembre de 2008): 585–86. http://dx.doi.org/10.1093/nass/nrn296.
Texto completoCAULKETT, P. W. R., G. JONES, M. MCPARTLIN, N. D. RENSHAW, S. K. STEWART y 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, n.º 34 (17 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199534183.
Texto completoBradbury, Robert H., John S. Major, Alec A. Oldham, Janet E. Rivett, David A. Roberts, Anthony M. Slater, David Timms y 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, n.º 9 (septiembre de 1990): 2335–42. http://dx.doi.org/10.1021/jm00171a006.
Texto completoSampognaro, Anthony J., Mark D. Wittman, Joan M. Carboni, Chiehying Chang, Ann F. Greer, Warren W. Hurlburt, John S. Sack y 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, n.º 17 (septiembre de 2010): 5027–30. http://dx.doi.org/10.1016/j.bmcl.2010.07.045.
Texto completoBRADBURY, R. H., J. S. MAJOR, A. A. OLDHAM, J. E. RIVETT, D. A. ROBERTS, A. M. SLATER, D. TIMMS y 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, n.º 8 (23 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199108220.
Texto completoFocken, 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, n.º 11 (8 de mayo de 2018): 4810–31. http://dx.doi.org/10.1021/acs.jmedchem.7b01826.
Texto completoRoma, Giorgio, Giancarlo Grossi, Mario Di Braccio, Daniela Piras, Vigilio Ballabeni, Massimiliano Tognolini, Simona Bertoni y 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, n.º 8 (agosto de 2008): 1665–80. http://dx.doi.org/10.1016/j.ejmech.2007.10.010.
Texto completoKumar, Sachin, Sukhbir Lal Khokra y Akash Yadav. "Triazole analogues as potential pharmacological agents: a brief review". Future Journal of Pharmaceutical Sciences 7, n.º 1 (25 de mayo de 2021). http://dx.doi.org/10.1186/s43094-021-00241-3.
Texto completoLal, Kashmiri, Aman Kumar, Yajat Rohila y Vijay Kumar. "A Mini Review on Pharmacological Significance of Isatin-1,2,3-Triazole Hybrids". Current Topics in Medicinal Chemistry 23 (2 de febrero de 2023). http://dx.doi.org/10.2174/1568026623666230202160925.
Texto completoPerissutti, Elisa, Francesco Frecentese, Ferdinando Fiorino, Beatrice Severino, Donatella Cirillo, Vincenzo Santagada y 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, n.º 47 (20 de noviembre de 2007). http://dx.doi.org/10.1002/chin.200747133.
Texto completo"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, n.º 4 (17 de octubre de 2021): 5217–33. http://dx.doi.org/10.33263/briac124.52175233.
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