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1Academic Journal
المؤلفون: Lucia Sofrankova, Jana Spaldova, Pavol Stefik, Branislav Pavilek, Dusan Bortnak, Lucia Pavlikova, Ivana Zidekova, Daniel Vegh, Viktor Milata, Albert Breier, Zdena Sulova
المصدر: European Journal of Medicinal Chemistry Reports, Vol 13, Iss , Pp 100246- (2025)
مصطلحات موضوعية: 5-Aminopyrazoles, Cancer, Cell death, P-glycoprotein, Pharmacy and materia medica, RS1-441, Other systems of medicine, RZ201-999
Relation: http://www.sciencedirect.com/science/article/pii/S2772417425000020; https://doaj.org/toc/2772-4174; https://doaj.org/article/bf69d371f88e4bee9ed53481f3a376e9
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2Academic Journal
المؤلفون: Federica Rapetti, Andrea Spallarossa, Eleonora Russo, Debora Caviglia, Carla Villa, Bruno Tasso, Maria Grazia Signorello, Camillo Rosano, Erika Iervasi, Marco Ponassi, Chiara Brullo
المصدر: Molecules, Vol 29, Iss 10, p 2298 (2024)
مصطلحات موضوعية: 5-aminopyrazoles, MTT test, anti-cancer activity, DPPH, ROS, druglike properties, Organic chemistry, QD241-441
Relation: https://www.mdpi.com/1420-3049/29/10/2298; https://doaj.org/toc/1420-3049; https://doaj.org/article/f972d7ba951b4953b48e4c2552e77869
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3Academic Journal
المؤلفون: Chiara Brullo, Debora Caviglia, Andrea Spallarossa, Silvana Alfei, Scott G. Franzblau, Bruno Tasso, Anna Maria Schito
المصدر: Pharmaceutics; Volume 14; Issue 9; Pages: 1770
مصطلحات موضوعية: pyrazole, 5-aminopyrazoles, antibacterial activity, Gram-positive species, Staphylococcus genus, in silico pharmacokinetic properties prediction
وصف الملف: application/pdf
Relation: Biopharmaceutics; https://dx.doi.org/10.3390/pharmaceutics14091770
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4Academic Journal
المؤلفون: Abdallah AEM, Elgemeie GH
المصدر: Drug Design, Development and Therapy, Vol Volume 12, Pp 1785-1798 (2018)
مصطلحات موضوعية: Pyrazolo[1, 5-a]pyrimidines, 5-aminopyrazoles, 2-(hydroxymethylene)-1-cycloalkanones, 2-formylcycloalkanones, antimicrobial, docking studies., Therapeutics. Pharmacology, RM1-950
وصف الملف: electronic resource
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5Academic Journal
المؤلفون: Ranjana Aggarwal, Suresh Kumar
المصدر: Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 203-242 (2018)
مصطلحات موضوعية: 5-aminopyrazoles, fused pyrazole derivatives, pyrazolopyridines, pyrazolopyrimidines, pyrazolotriazines, Science, Organic chemistry, QD241-441
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1860-5397
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6Academic Journal
المصدر: Molecules; Volume 25; Issue 18; Pages: 4169
مصطلحات موضوعية: thiocyanate group, 5-aminopyrazoles, 1,3-dicarbonyl compounds, pyrazolo[1,5- a ]pyrimidines, anodic C–H thiocyanation, condensation, cyclic voltammetry
جغرافية الموضوع: agris
وصف الملف: application/pdf
Relation: Organic Chemistry; https://dx.doi.org/10.3390/molecules25184169
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7Academic Journal
المؤلفون: Mario A. Macías, Jessica Orrego-Hernández, Jaime Portilla
المصدر: Acta Crystallographica Section E: Crystallographic Communications, Vol 72, Iss 11, Pp 1672-1674 (2016)
مصطلحات موضوعية: crystal structure, pharmaceutical compound, 5-aminopyrazoles, nucleophilic substitution, hydrogen bonding, Crystallography, QD901-999
وصف الملف: electronic resource
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8Academic Journal
المؤلفون: Zemlyana, N. I., Karnozhitska, T. M., Pavlovska, T. L., Mazepa, O. V., Musatov, V. I., Lipson, V. V.
المصدر: Журнал органічної та фармацевтичної хімії; Том 16 № 4(64) (2018); 3-10 ; Journal of Organic and Pharmaceutical Chemistry; Vol. 16 No. 4(64) (2018); 3-10 ; Журнал органической и фармацевтической химии; Том 16 № 4(64) (2018); 3-10 ; 2518-1548 ; 2308-8303
مصطلحات موضوعية: pyrazolo[3, 4-b]pyridine-4-spiroindolinones, 3-(5-aminopyrazol-4-yl)-3-hydroxy-2-oxindolines, isatins, 5-aminopyrazoles, 2-dimethyl-1, 3-dioxane-4, 6-dione, domino-reactions, UDC, 547.859.1, пиразоло[3, 4-b]пиридин-4-спироиндолиноны, 3-(5-аминопиразол-4-ил)-3-гидрокси-2-оксиндолины, изатины, 5-аминопиразолы, 2-диметил-1, 3-диоксан-4, 6-дион, домино-реакции, УДК, піразоло[3, 4-b]піридин-4-спіроіндолінони, 3-(5-амінопіразол-4-іл)-3-гідрокси-2-оксіндоліни, ізатини, 5-амінопіразоли, 3-діоксан-4, 6-діон, доміно-реакції
Time: 2
وصف الملف: application/pdf
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9
المؤلفون: Lozano Oviedo, John Jair
المساهمون: Cuervo Prado, Paola Andrea, Grupo de Estudios en Síntesis y Aplicaciones de Compuestos Heterocíclicos (Gesach)
المصدر: Repositorio UN
Universidad Nacional de Colombia
instacron:Universidad Nacional de Colombiaمصطلحات موضوعية: Electron-rich olefins, olefinas ricas en electrones, síntesis, Química orgánica-Síntesis, Multicomponent, Compuestos heterocíclicos, 5-aminopirazoles, Pyrazolopyridine, 5-aminopyrazoles, 540 - Química y ciencias afines, Microwave reaction, pirazolopiridinas, Heterocyclic Compounds, in silico, Organic compounds-Synthesis, GABA-A receptor, receptor GABA-A, microondas
وصف الملف: 143 páginas; application/pdf
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10Academic Journal
المؤلفون: Ranjana Aggarwal, Vinod Kumar, Rajiv Kumar, Shiv P. Singh
المصدر: Beilstein Journal of Organic Chemistry, Vol 7, Iss 1, Pp 179-197 (2011)
مصطلحات موضوعية: alkylidenemalononitriles, 5-aminopyrazoles, hydrazines, β-ketonitriles, malononitriles, Science, Organic chemistry, QD241-441
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1860-5397
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11Dissertation/ Thesis
المؤلفون: Lozano Oviedo, John Jair
المساهمون: Cuervo Prado, Paola Andrea, Grupo de Estudios en Síntesis y Aplicaciones de Compuestos Heterocíclicos (Gesach)
مصطلحات موضوعية: 540 - Química y ciencias afines, Compuestos heterocíclicos, Química orgánica-Síntesis, Heterocyclic Compounds, Organic compounds-Synthesis, in silico, pirazolopiridinas, microondas, receptor GABA-A, síntesis, 5-aminopirazoles, olefinas ricas en electrones, 5-aminopyrazoles, Pyrazolopyridine, Electron-rich olefins, Multicomponent, Microwave reaction, GABA-A receptor
وصف الملف: 143 páginas; application/pdf
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Med. Chil. 2014, 142 (10), 1297–1305. https://doi.org/10.4067/S0034-98872014001000010.; Sullivan, P. F.; Neale, M. C.; Kendler, K. S. Genetic Epidemiology of Major Depression: Review and Meta-Analysis. Am. J. Psychiatry 2000, 157 (10), 1552–1562. https://doi.org/10.1176/APPI.AJP.157.10.1552.; Caspi, A.; Sugden, K.; Moffitt, T. E.; Taylor, A.; Craig, I. W.; Harrington, H. L.; McClay, J.; Mill, J.; Martin, J.; Braithwaite, A.; Poulton, R. Influence of Life Stress on Depression: Moderation by a Polymorphism in the 5-HTT Gene. Science (80-. ). 2003, 301 (5631), 386–389. https://doi.org/10.1126/SCIENCE.1083968.; Diaz Villa, B. A.; González González, C. Actualidades En Neurobiología de La Depresión. Rev Lationam Psiquitría 2012, 11 (3), 106–115.; Heim, C.; Nemeroff, C. B. The Role of Childhood Trauma in the Neurobiology of Mood and Anxiety Disorders: Preclinical and Clinical Studies. Biol. Psychiatry 2001, 49 (12), 1023–1039. https://doi.org/10.1016/S0006-3223(01)01157-X.; Gavernet, L. Introducción a La Química Medicinal; Editorial de la Universidad Nacional de La Plata (EDULP): Ciudad de la plata, 2021. https://doi.org/10.35537/10915/114312.; Medina-Franco, J. L.; Fernán-Dezde Gortari, E.; Jesús Naveja, J. Avances En El Diseño de Fármacos Asistido Por Computadora. Educ. Química 2015, 26 (3), 180–186. https://doi.org/10.1016/J.EQ.2015.05.002.; Saldívar-González, F.; Prieto-Martínez, F. D.; Medina-Franco, J. L. Descubrimiento y Desarrollo de Fármacos: Un Enfoque Computacional. Educ. Química 2017, 28 (1), 51–58. https://doi.org/10.1016/J.EQ.2016.06.002.; Rojas, W. M.; Oviedo, K. N. Acoplamiento Inverso Y Mapeo De Farmacóforo Como Herramientas Para Encontrar Nuevos Blancos Farmacológicos De Compuestos Naturales. Rev. la Acad. Colomb. Ciencias Exactas, Físicas y Nat. 2012, 36 (140), 411–420.; Claudio Viegas-Junior; Eliezer J. Barreiro; Carlos Alberto Manssour Fraga. Molecular Hybridization: A Useful Tool in the Design of New Drug Prototypes. Curr. Med. Chem. 2007, 14 (17), 1829–1852. https://doi.org/10.2174/092986707781058805.; Umar, T.; Shalini, S.; Raza, M. K.; Gusain, S.; Kumar, J.; Seth, P.; Tiwari, M.; Hoda, N. A Multifunctional Therapeutic Approach: Synthesis, Biological Evaluation, Crystal Structure and Molecular Docking of Diversified 1H-Pyrazolo[3,4-b]Pyridine Derivatives against Alzheimer’s Disease. Eur. J. Med. Chem. 2019, 175, 2–19. https://doi.org/10.1016/j.ejmech.2019.04.038.; Ansari, A.; Ali, A.; Asif, M.; Shamsuzzaman. Review: Biologically Active Pyrazole Derivatives. New J. Chem. 2016, 41 (1), 16–41. https://doi.org/10.1039/c6nj03181a.; Karrouchi, K.; Radi, S.; Ramli, Y.; Taoufik, J.; Mabkhot, Y. N.; Al-Aizari, F. A.; Ansar, M. Synthesis and Pharmacological Activities of Pyrazole Derivatives: A Review. Molecules. MDPI AG 2018. https://doi.org/10.3390/molecules23010134.; Tripathi, A. C.; Upadhyay, S.; Paliwal, S.; Saraf, S. K. Derivatives of 4,5-Dihydro (1H) Pyrazoles as Possible MAO-A Inhibitors in Depression and Anxiety Disorders: Synthesis, Biological Evaluation and Molecular Modeling Studies. Med. Chem. Res. 2018, 27 (5), 1485–1503. https://doi.org/10.1007/s00044-018-2167-z.; Faisal, M.; Saeed, A.; Hussain, S.; Dar, P.; Larik, F. A. Recent Developments in Synthetic Chemistry and Biological Activities of Pyrazole Derivatives. J. Chem. Sci. 2019, 131 (8). https://doi.org/10.1007/s12039-019-1646-1.; Yadav, J. S.; Purushothama Rao, P.; Sreenu, D.; Rao, R. S.; Naveen Kumar, V.; Nagaiah, K.; Prasad, A. R. Sulfamic Acid: An Efficient, Cost-Effective and Recyclable Solid Acid Catalyst for the Friedlander Quinoline Synthesis. Tetrahedron Lett. 2005, 46 (42), 7249–7253. https://doi.org/10.1016/j.tetlet.2005.08.042.; Gervasini, G.; Carrillo, J.; Benitez, J. Importancia Del Citocromo P-450 En Terapéutica Farmacológica. 2022.; Ritchie, T. J.; Ertl, P.; Lewis, R. The Graphical Representation of ADME-Related Molecule Properties for Medicinal Chemists. Drug Discov. Today 2011, 16 (1–2), 65–72. https://doi.org/10.1016/j.drudis.2010.11.002.; Brenk, R.; Schipani, A.; James, D.; Krasowski, A.; Gilbert, I. H.; Frearson, J.; Wyatt, P. G. Lessons Learnt from Assembling Screening Libraries for Drug Discovery for Neglected Diseases. ChemMedChem 2008, 3 (3), 435–444. https://doi.org/10.1002/cmdc.200700139.; Smith, G. B.; Olsen, R. W. Functional Domains of GABAA Receptors. Trends Pharmacol. Sci. 1995, 16 (5), 162–168. https://doi.org/10.1016/S0165-6147(00)89009-4.; Nitro bioisosteres. %7C News %7C Cambridge MedChem Consulting https://www.cambridgemedchemconsulting.com/news/index_files/e257c4796cad57a277e5b735ea47bf96-136.html (accessed May 4, 2022).; Hügel, H. Microwave Multicomponent Synthesis. Molecules 2009, 14 (12), 4936–4972. https://doi.org/10.3390/molecules14124936.; Alegre, J. V.; Marqués, E.; Herrera, R. P. Introduction. In Multicomponent Reactions; John Wiley & Sons, Inc: Hoboken, NJ, 2015; pp 1–15. https://doi.org/10.1002/9781118863992.ch1.; Sharma, A.; Appukkuttan, P.; Van der Eycken, E. Microwave-Assisted Synthesis of Medium-Sized Heterocycles. Chem. Commun. 2012, 48 (11), 1623–1637. https://doi.org/10.1039/c1cc15238f.; Alcázar, J.; de M. Muñoz, J. Microwave-Assisted Continuous Flow Organic Synthesis (MACOS). In Microwaves in Organic Synthesis; Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, Germany, 2013; Vol. 2, pp 1173–1204. https://doi.org/10.1002/9783527651313.ch25.; Perreux, L.; Loupy, A. Nonthermal Effects of Microwaves in Organic Synthesis. Microwaves Org. Synth. Second Ed. 2008, 1, 134–218. https://doi.org/10.1002/9783527619559.ch4.; Kappe, C. O.; Stadler, A. Microwaves in Organic and Medicinal Chemistry; Wiley Blackwell, 2006; Vol. 25. https://doi.org/10.1002/3527606556.; Parada, C.; Morán, E. Microwave-Assisted Synthesis and Magnetic Study of Nanosized Ni/NiO Materials. Chem. Mater. 2006, 18 (11), 2719–2725. https://doi.org/10.1021/cm0511365.; Leadbeater, N. E. Organic Synthesis Using Microwave Heating. In Comprehensive Organic Synthesis: Second Edition; Elsevier Ltd., 2014; Vol. 9, pp 234–286. https://doi.org/10.1016/B978-0-08-097742-3.00920-4.; Kappe, C. O.; Pieber, B.; Dallinger, D. Microwave Effects in Organic Synthesis: Myth or Reality? Angew. Chemie Int. Ed. 2013, 52 (4), 1088–1094. https://doi.org/10.1002/anie.201204103.; Perreux, L.; Loupy, A.; Petit, A. Nonthermal Effects of Microwaves in Organic Synthesis. In Microwaves in Organic Synthesis; Wiley-VCH Verlag GmbH & Co. KGaA: Weinheim, Germany, 2013; Vol. 1, pp 127–207. https://doi.org/10.1002/9783527651313.ch4.; Corey, E. . (harvard university); Li, J. Name Reactions in Heterocyclic Chemistry; Li, J., Ed.; 2004.; paquette, L. Fundamentos de Química Heterocíclica; Universidad estatal de Ohio, Ed.; Limusa Noriega, 2000.; Lager, E.; Nilsson, J.; Østergaard Nielsen, E.; Nielsen, M.; Liljefors, T.; Sterner, O. Affinity of 3-Acyl Substituted 4-Quinolones at the Benzodiazepine Site of GABAA Receptors. Bioorg. Med. Chem. 2008, 16 (14), 6936–6948. https://doi.org/10.1016/j.bmc.2008.05.049.; Shi, F.; Zhang, J.; Tu, S.; Jia, R.; Zhang, Y.; Jiang, B.; Jiang, H. An Efficient Synthesis of New Class of Pyrazolo[3,4- b ]Pyridine-6-One Derivatives by a Novel Cascade Reaction. J. Heterocycl. Chem. 2007, 44 (5), 1013–1017. https://doi.org/10.1002/jhet.5570440506.; Chen, Z.; Shi, Y.; Shen, Q.; Xu, H.; Zhang, F. Facile and Efficient Synthesis of Pyrazoloisoquinoline and Pyrazolopyridine Derivatives Using Recoverable Carbonaceous Material as Solid Acid Catalyst. Tetrahedron Lett. 2015, 56 (33), 4749–4752. https://doi.org/10.1016/j.tetlet.2015.06.044.; Shi, C.-L.; Chen, H.; Shi, D.-Q. An Efficient One-Pot Synthesis of Pyrazolo[3,4-b]Pyridinone Derivatives Catalyzed by L-Proline. J. Heterocycl. Chem. 2011, 48 (2), 351–354. https://doi.org/10.1002/jhet.573.; Orlov, V. D.; Kiroga, K.; Kolos, N. N. Synthesis of Aromatic Pyrazolo[4,5-b]Pyridine Derivatives. Chem. Heterocycl. Compd. 1988 239 1987, 23 (9), 997–1001. https://doi.org/10.1007/BF00475369.; Daniela Ahumada, C.; Segovia-Paccini, A.; Navas, G. R. S. Los 5-Aminopirazoles Como Bloque de Construcción de Compuestos Heterocíclicos Fusionados. Rev. la Acad. Colomb. Ciencias Exactas, Físicas y Nat. 2019, 43 (168), 531–538. https://doi.org/10.18257/RACCEFYN.762.; Gálvez, J.; Quiroga, J.; Insuasty, B.; Abonia, R. Microwave-Assisted and Iodine Mediated Synthesis of 5-n-Alkyl-Cycloalkane[d]-Pyrazolo[3,4-b]Pyridines from 5-Aminopyrazoles and Cyclic Ketones. Tetrahedron Lett. 2014, 55 (12), 1998–2002. https://doi.org/10.1016/j.tetlet.2014.02.015.; Chu, X. Q.; Wang, S. Y.; Ji, S. J. Recyclable NaHSO 4 Catalyzed Alkylation of Tert-Enamides with Indoles or Amines in Water: Facile Construction of Pharmaceutically Analogous Bis-Alkaloid Scaffolds. RSC Adv. 2013, 3 (22), 8380–8387. https://doi.org/10.1039/c3ra40833g.; Ziyaei Halimehjani, A.; Goudarzi, M.; Lotfi Nosood, Y. Alkylation of Aromatic Amines by Tert-Enamides: Direct Access to Protected Aminals. Synth. Commun. 2017, 47 (21), 2022–2029. https://doi.org/10.1080/00397911.2017.1363241.; Zaytsev, V. P.; Zubkov, F. I.; Toze, F. A. A.; Orlova, D. N.; Eliseeva, M. N.; Grudinin, D. G.; Nikitina, E. V.; Varlamov, A. V. 5-Amido- and 5-Amino-Substituted Epoxyisoindolo[2,1-a]Tetrahydroquinolines and 10-Carboxylic Acids: Their Synthesis and Reactivity. J. Heterocycl. Chem. 2013, 50 (SUPPL.1). https://doi.org/10.1002/jhet.1024.; Khadem, S.; Udachin, K. A.; Enright, G. D.; Prakesch, M.; Arya, P. One-Pot Construction of Isoindolo[2,1-a]Quinoline System. Tetrahedron Lett. 2009, 50 (48), 6661–6664. https://doi.org/10.1016/j.tetlet.2009.09.075.; Dagousset, G.; Drouet, F.; Masson, G.; Zhu, J. Chiral Brønsted Acid-Catalyzed Enantioselective Multicomponent Mannich Reaction: Synthesis of Anti-1,3-Diamines Using Enecarbamates as Nucleophiles. Org. Lett. 2009, 11 (23), 5546–5549. https://doi.org/10.1021/ol9023985; Terada, M.; Sorimachi, K. Enantioselective Friedel-Crafts Reaction of Electron-Rich Alkenes Catalyzed by Chiral Brønsted Acid. J. Am. Chem. Soc. 2007, 129 (2), 292–293. https://doi.org/10.1021/ja0678166.; Halimehjani, A. Z.; Dadras, A.; Ramezani, M.; Shamiri, E. V.; Hooshmand, S. E.; Hashemi, M. M. Synthesis of Dithiocarbamates by Markovnikov Addition Reaction in PEG and Their Application in Amidoalkylation of Naphthols and Indoles. J. Braz. Chem. Soc. 2015, 26 (7), 1500–1508. https://doi.org/10.5935/0103-5053.20150119.; Halimehjani, A.; Goudarzi, M.; Nosood, Y. Alkylation of Aromatic Amines by Tert-Enamides: Direct Access to Protected Aminals. Synth. Commun. 2017, 47 (21), 2022–2029. https://doi.org/10.1080/00397911.2017.1363241.; Tamaddon, F.; Khoobi, M.; Keshavarz, E. (P2O5/SiO2): A Useful Heterogeneous Alternative for the Ritter Reaction. Tetrahedron Lett. 2007, 48 (21), 3643–3646. https://doi.org/10.1016/J.TETLET.2007.03.134.; Reddy, P. N.; Reddy, B. V. S.; Padmaja, P. Current Organic Synthesis Current Organic Synthesis SCIENCE BENTHAM Send Orders for Reprints to Reprints@benthamscience.Ae Emerging Role of Green Oxidant I 2 /DMSO in Organic Synthesis. Curr. Org. Synth. 2018, 15, 815–838. https://doi.org/10.2174/1570179415666180530121312.; Becerra-Rivas, C.; Cuervo-Prado, P.; Orozco-Lopez, F. Efficient Catalyst-Free Tricomponent Synthesis of New Spiro[Cyclohexane-1,4′-Pyrazolo[3,4- e ][1, 4]Thiazepin]-7′(6′ H )-Ones. Synth. Commun. 2019, 49 (3), 367–376. https://doi.org/10.1080/00397911.2018.1554143.; Breugst, M.; von der Heiden, D. Mechanisms in Iodine Catalysis. Chem. - A Eur. J. 2018, 24 (37), 9187–9199. https://doi.org/10.1002/chem.201706136.; Yang, H.; Lou, C.; Sun, L.; Li, J.; Cai, Y.; Wang, Z.; Li, W.; Liu, G.; Tang, Y. AdmetSAR 2.0: Web-Service for Prediction and Optimization of Chemical ADMET Properties. Bioinformatics 2019, 35 (6), 1067–1069. https://doi.org/10.1093/BIOINFORMATICS/BTY70; Daina, A.; Michielin, O.; Zoete, V. SwissADME: A Free Web Tool to Evaluate Pharmacokinetics, Drug-Likeness and Medicinal Chemistry Friendliness of Small Molecules. Sci. Rep. 2017, 7. https://doi.org/10.1038/SREP42717.; Morris, G. M.; Ruth, H.; Lindstrom, W.; Sanner, M. F.; Belew, R. K.; Goodsell, D. S.; Olson, A. J. AutoDock4 and AutoDockTools4: Automated Docking with Selective Receptor Flexibility. J. Comput. Chem. 2009, 30 (16), 2785. https://doi.org/10.1002/JCC.21256.; Allen, W. J.; Balius, T. E.; Mukherjee, S.; Brozell, S. R.; Moustakas, D. T.; Lang, P. T.; Case, D. A.; Kuntz, I. D.; Rizzo, R. C. DOCK 6: Impact of New Features and Current Docking Performance. J. Comput. Chem. 2015, 36 (15), 1132–1156. https://doi.org/10.1002/JCC.23905.; LADIN, J. J. H.; Fabian Orozco López. DISEÑO, SÍNTESIS Y CARACTERIZACIÓN DE COMPUESTOS ESPIROTIAZAHETEROCÍCLICOS CON POTENCIAL ACTIVIDAD SOBRE SISTEMA NERVIOSO CENTRAL (SNC), Universidad Nacional de Colombia, 2019.; Bamoniri, A.; Mirjalili, B. B. F.; Jafari, A. A.; Abasaltian, F. Synthesis of 1,3,5-Tri-Substituted Pyrazoles Promoted by P2O5.SiO2. Iran. J. Catal. 2012, 2 (2), 75–78. https://doi.org/10.31857/s042485702109005x.; https://repositorio.unal.edu.co/handle/unal/82230; Universidad Nacional de Colombia; Repositorio Institucional Universidad Nacional de Colombia; https://repositorio.unal.edu.co/
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12Academic Journal
المؤلفون: Ashraf HASSAN, Taghrid HAFEZ, Souad OSMAN
المصدر: Scientia Pharmaceutica; Volume 83; Issue 1; Pages: 27-39
مصطلحات موضوعية: N -Substituted cyanoacetamide, Ketene N, S -acetals, Pyrazolo[1,5- a ]pyrimidines, 5-Aminopyrazoles, Cytotoxic activity
وصف الملف: application/pdf
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13
المصدر: Molecules, Vol 25, Iss 4169, p 4169 (2020)
Molecules
Volume 25
Issue 18مصطلحات موضوعية: Pyrimidine, Pharmaceutical Science, Ring (chemistry), 5-aminopyrazoles, Analytical Chemistry, lcsh:QD241-441, chemistry.chemical_compound, Thiocyanate ion, lcsh:Organic chemistry, Drug Discovery, Polymer chemistry, 1,3-dicarbonyl compounds, pyrazolo[1,5-a]pyrimidines, thiocyanate group, Physical and Theoretical Chemistry, Organic Chemistry, Condensation, Chemical condensation, Acceptor, cyclic voltammetry, condensation, chemistry, Chemistry (miscellaneous), Molecular Medicine, Cyclic voltammetry, anodic C–H thiocyanation
وصف الملف: application/pdf
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14
المصدر: Molecules
مصطلحات موضوعية: Molecular Structure, Chemistry Techniques, Synthetic, Carbon, Electrolysis, Article, 5-aminopyrazoles, cyclic voltammetry, pyrazolo[1,5-a]pyrimidines, Structure-Activity Relationship, condensation, Pyrimidines, 1,3-dicarbonyl compounds, Electrochemistry, Pyrazoles, thiocyanate group, anodic C–H thiocyanation, Electrodes, Thiocyanates, Hydrogen
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15Academic Journal
المؤلفون: Hashmi, I.A., Feist, H., Michalik, M., Reinke, H., Peseke, K.
مصطلحات موضوعية: Reversed' C-Nucleoside Analogues, 5-Aminopyrazoles, Benzo[4,5]imidazo[1,2-a]pyridine, Pyrazolo[1,5-a]pyrimidines, Pyrimidines
Time: 540
وصف الملف: application/pdf; text/plain; charset=utf-8
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16
المؤلفون: Suresh Kumar, Ranjana Aggarwal
المصدر: Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 203-242 (2018)مصطلحات موضوعية: 010405 organic chemistry, Chemistry, Condensation, Organic Chemistry, Review, fused pyrazole derivatives, 010402 general chemistry, 01 natural sciences, Combinatorial chemistry, 5-aminopyrazoles, 0104 chemical sciences, lcsh:QD241-441, lcsh:Organic chemistry, Organic reaction, pyrazolopyrimidines, lcsh:Q, lcsh:Science, pyrazolopyridines, pyrazolotriazines
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17
المؤلفون: Amira E M, Abdallah, Galal H, Elgemeie
المصدر: Drug Design, Development and Therapy
مصطلحات موضوعية: Antifungal Agents, Molecular Structure, 2-(hydroxymethylene)-1-cycloalkanones, Proton Magnetic Resonance Spectroscopy, Cycloparaffins, docking studies, Gram-Positive Bacteria, 2-formylcycloalkanones, Mass Spectrometry, 5-aminopyrazoles, Anti-Bacterial Agents, pyrazolo[1,5-a]pyrimidines, Molecular Docking Simulation, Structure-Activity Relationship, antibacterial, Pyrimidines, Disk Diffusion Antimicrobial Tests, Drug Design, Candida albicans, Gram-Negative Bacteria, Spectroscopy, Fourier Transform Infrared, Pyrazoles, antifungal, Aspergillus flavus, Original Research
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18
المؤلفون: Jessica Orrego-Hernández, Jaime Portilla, Mario A. Macías
المصدر: Acta Crystallographica Section E: Crystallographic Communications, Vol 72, Iss 11, Pp 1672-1674 (2016)
Acta Crystallographica Section E: Crystallographic Communicationsمصطلحات موضوعية: crystal structure, Crystal structure, Dihedral angle, Pyrazole, 010402 general chemistry, 01 natural sciences, Microwave assisted, pharmaceutical compound, 5-aminopyrazoles, Caesium carbonate, Research Communications, Catalysis, lcsh:Chemistry, chemistry.chemical_compound, Polymer chemistry, Nucleophilic substitution, Organic chemistry, General Materials Science, Quantitative Biology::Biomolecules, 010405 organic chemistry, Chemistry, Hydrogen bond, General Chemistry, hydrogen bonding, Condensed Matter Physics, 0104 chemical sciences, lcsh:QD1-999, 5-aminopyrazoles, nucleophilic substitution
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19Dissertation/ Thesis
المؤلفون: 劉柏麟, Po-Lin Liu
المساهمون: 藥物化學研究所碩士班
مصطلحات موضوعية: Vilsmeier反應, 5-氨基?紹, ?紹?[3,4-d]嘧啶, 甲?謋??承I, Vilsmeier reaction, 5-Aminopyrazoles, Pyrazolo[3,4-d]pyrimidine, Formamidine, Formamide
Relation: http://ir.cmu.edu.tw/ir/handle/310903500/54329; http://ir.cmu.edu.tw/ir/bitstream/310903500/54329/2/index.html; http://ir.cmu.edu.tw/ir/bitstream/310903500/54329/3/index.html; http://ir.cmu.edu.tw/ir/bitstream/310903500/54329/1/index.html
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20
المؤلفون: Chang, Chun-Hsi, 蔡建鈞, Tsai, Henry Jan-Jen, Huang, Yu-Ying, Lin, Hui-Yi, Wang, Li-Ya, Wu, Tian-Shung, Wong, Fung Fuh
المساهمون: 保健營養生技學系
مصطلحات موضوعية: Vilsmeier reaction, 5-Aminopyrazoles, Pyrazolo[3,4-d]pyrimidine, Formamidine, Formamide
Relation: TETRAHEDRON, 69(4):1378-1386.; http://asiair.asia.edu.tw/ir/handle/310904400/25284; http://asiair.asia.edu.tw/ir/bitstream/310904400/25284/1/index.html