dcterms.isReferencedBy |
Kam, D., Kim, K., Kim, H.-S., Liu, H.K., Studies on film formation on cathodes using pyrazole derivatives as electrolyte additives in the Li-ion battery (2009) Electrochem. Commun., 11, pp. 1657-1660; Keter, F.K., Darkwa, J., Perspective: The potential of pyrazole-based compounds in medicine Biometals, 2012 (25), pp. 9-21; Yutilov, Y.M., Smolyar, N.N., Minkina, L., Synthesis of 3-(3 -Aminobenzoylamido)-1-(2 ,4 ,6 -trichlorophenyl) pyrazol-5-one, an intermediate in the synthesis of the purple component of color photographic materials (2005) Russ. J. Appl. Chem., 78, pp. 278-280; Tingle, C.C., Rother, J.A., Dewhurst, C.F., Lauer, S., King, W.J., Fipronil: Environmental fate, ecotoxicology, and human health concerns (2003) Rev. Environ. Contam. Toxicol., 176, pp. 1-66; Metwally, M.A., Abdel-Galil, E., Metwally, A., Amer, F.A., New azodisperse dyes with thiazole, thiophene, pyridone and pyrazolone moiety for dyeing polyester fabrics (2012) Dyes Pigment., 92, pp. 902-908; Aly, H.M., El-Gazzar, M.G., Novel pyrazole derivatives as anticancer and radiosensitizing agents (2012) Arzneimittelforschung, 62, pp. 105-112; Puthiyapurayil, P., Poojary, B., Chikkanna, C., Buridipad, S.K., Design, synthesis and biological evaluation of a novel series of 1,3,4-oxadiazole bearing N-methyl-4-(trifluoromethyl) phenyl pyrazole moiety as cytotoxic agents (2012) Eur. J. Med. Chem., 53, pp. 203-210; Hassan, G.S., Kadry, H.H., Abou-Seri, S.M., Ali, M.M., Mahmoud, A.E., Synthesis and in vitro cytotoxic activity of novel pyrazolo[3,4-d]pyrimidines and related pyrazole hydrazones toward breast adenocarcinoma MCF-7 cell line (2011) Bioorg. Med. Chem., 19, pp. 6808-6817; El-Zahar, M.I., El-Karim, S.S.A., Haiba, M.E., Khedr, M.A., Synthesis, antitumor activity and molecular docking study of novel benzofuran-2-yl pyrazole pyrimidine derivatives (2011) Acta Pol. Pharm., 68, pp. 357-373; El-Gamal, M.I., Sim, T.B., Hong, J.H., Cho, J.-H., Yoo, K.H., Oh, C.-H., Synthesis of 1H-pyrazole-1-carboxamide derivatives and their antiproliferative activity against melanoma cell line (2011) Arch. Pharm., 344, p. 197; Sharshira, E.M., Hamada, N.M.M., Synthesis and antimicrobial evaluation of some pyrazole derivatives (2012) Molecules, 17, pp. 4962-4971; Ragavan, R.V., Vijayakumar, V., Kumari, N.S., Synthesis and antimicrobial activities of novel 1,5-diaryl pyrazoles (2010) Eur. J. Med. Chem., 45, pp. 1173-1180; Ouyang, G., Chen, Z., Cai, X.-J., Song, B.-A., Bhadury, P.S., Yang, S., Jin, L.-H., Zeng, S., Synthesis and antiviral activity of novel pyrazole derivatives containing oxime esters group (2008) Bioorg. Med. Chem., 16, pp. 9699-9707; Sanchez-Moreno, M., Gomez-Contreras, F., Navarro, P., Marin, C., Ramirez-Macias, I., Olmo, F., Sanz, A.M., Yunta, M.J., In vitro leishmanicidal activity of imidazole- or pyrazole-based benzo[g]phthalazine derivatives against Leishmania infantum and Leishmania braziliensis species (2012) J. Antimicrob. Chemoth., 67, pp. 387-397; El-Din, M.M.M., Senbel, A.M., Bistawroos, A.A., El-Mallah, A., El-Din, N.A.N., Bekhit, A.A., El Razik, H.A.A., A novel COX-2 inhibitor pyrazole derivative proven effective as an anti-inflammatory and analgesic drug (2011) Basic Clin. Pharmacol., 108, pp. 263-273; Raffa, D., Migliara, O., Maggio, B., Plescia, F., Cascioferro, S., Cusimano, M.G., Tringali, G., Plescia, F., Pyrazolobenzotriazinone derivatives as COX inhibitors: Synthesis, biological activity, and molecularmodeling studies (2010) Arch. Pharm. Chem. Life Sci., 10, pp. 631-638; Tomazetti, J., Avila, D.S., Ferreira, A.P., Martins, J.S., Souza, F.R., Royer, C., Baker yeast-induced fever in young rats: Characterization and validation of an animal model for antipyretics screening (2005) J. Neurosci. Methods, 147, pp. 29-35; Dekhane, D.V., Pawar, S.S., Gupta, S., Shingare, M.S., Patil, C.R., Thore, S.N., Synthesis and anti-inflammatory activity of some new 4,5-dihydro-1,5-diaryl-1H-pyrazole-3-substituted-heteroazole derivatives (2011) Bioorg. Med. Chem. Lett., 21, pp. 6527-6532; Agrawal, R., Jain, P., Dikshit, S.N., Apixaban: A new player in the anticoagulant class (2012) Curr. Drug Targets, 13, pp. 863-875; Backhouse, K., Sarac, I., Shojaee-Moradie, F., Stolinski, M., Robertson, M.D., Frost, G.S., Bell, J.D., Russell-Jones, D., Fatty acid flux and oxidation are increased by rimonabant in obese women (2012) Metabolis, 61, pp. 1220-1223; Ranu, B.C., Jana, R., Sowmiah, S., An improved procedure for the three-component synthesis of highly substituted pyridines using ionic liquid (2007) J. Org. Chem., 72, pp. 3152-3154; Abbas, I.M., Gomha, S.M., Elaasser, M.M., Bauomi, M.A., Synthesis and biological evaluation of new pyridines containing imidazole moiety as antimicrobial and anticancer agents (2015) Turk. J. Chem., 39, pp. 334-346; Xu, W.C., Zhou, Q., Ashendel, C.L., Chang, C.T., Chang, C.J., Novel protein kinase C inhibitors: Synthesis and PKC inhibition of ?-substituted polythiophene derivatives (1999) Bioorg. Med. Chem. Lett., 9, pp. 2279-2282; Zhao, L.X., Moon, Y.S., Basnet, A., Kim, E.K., Jahng, Y., Park, J.G., Jeong, T.C., Lee, C.O., The discovery and synthesis of novel adenosine receptor (A2A) antagonists (2004) Bioorg. Med. Chem. Lett., 14, pp. 1333-1336; Zhao, L.X., Sherchan, J., Park, J.K., Jahng, Y., Jeong, B.S., Jeong, T.C., Lee, C.S., Lee, E.S., Synthesis, cytotoxicity and structure-activity relationship study of terpyridines (2006) Arch. Pharm. Res., 29, pp. 1091-1095; Son, J.K., Zhao, L.X., Basnet, A., Thapa, P., Karki, R., Na, Y., Jahng, Y., Lee, C.S., Synthesis of 2,6-diaryl-substituted pyridines and their antitumor activities (2008) Eur. J. Med. Chem., 43, pp. 675-682; Thapa, P., Karki, R., Choi, H.Y., Choi, J.H., Yun, M., Jeong, B.S., Jung, M.J., Cho, W.J., Synthesis of 2-(thienyl-2-yl or -3-yl)-4-furyl-6-aryl pyridine derivatives and evaluation of their topoisomerase I and II inhibitory activity, cytotoxicity, and structure�activity relationship (2010) Bioorg. Med. Chem., 18, pp. 2245-2254; Jeong, B.S., Choi, H.Y., Thapa, P., Karki, R., Lee, E., Nam, J.M., Na, Y., Lee, E.S., Synthesis, Topoisomerase I and II Inhibitory activity, cytotoxicity, and structure-activity relationship study of rigid analogues of 2,4,6-trisubstituted pyridine containing 5,6-dihydrobenzo[h]quinoline moiety (2011) Bull. Korean Chem. Soc., 32, pp. 303-306; Eryazici, I., Moorefield, C.N., Newkome, G.R., Square-Planar Pd(II), Pt(II), and Au(III) Terpyridine Complexes: Their Syntheses, Physical Properties, Supramolecular Constructs, and Biomedical Activities (2008) Chem. Rev., 108, pp. 1834-1895; Patel, K.K., Plummer, E.A., Darwish, M., Rodger, A., Hannon, M.J., Aryl substituted ruthenium bis-terpyridine complexes: Intercalation and groove binding with DNA (2002) J. Inorg. Biochem., 91, pp. 220-229; Weber, L., The application of multi-component reactions in drug discovery (2002) Curr. Med. Chem., 9, pp. 2085-2093; Hulme, C., Gore, V., Multi-component reactions: Emerging chemistry in drug discovery from xylocain to crixivan (2003) Curr. Med. Chem., 10, pp. 51-80; Nair, V., Rajesh, C., Vinod, A.U., Bindu, S., Sreekanth, A.R., Mathen, J.S., Balagopal, L., Strategies for heterocyclic construction via novel multicomponent reactions based on isocyanides and nucleophilic carbenes (2003) Acc. Chem. Res., 36, pp. 899-907; Andrade, C.K.Z., Barreto, A.S., Silva, W.A., Microwave assisted solvent-, support- and catalyst-free synthesis of enaminones (2008) Ark. Arch. Org. Chem., 12, pp. 226-232; Bortolini, O., D'Agostino, M., De Nino, A., Maiuolo, L., Nardi, M., Sindona, G., Solvent-free, microwave assisted 1,3-cycloaddition of nitrones with vinyl nucleobases for the synthesis of N,O-nucleosides (2008) Tetrahedron, 64, pp. 8078-8081; Ganesan, S., Muthuraaman, B., Madhavan, J., Mathew, V., Maruthamuthu, P., Suthanthiraraj, S.A., The use of 2,6-bis (N-pyrazolyl) pyridine as an efficient dopant in conjugation with poly(ethylene oxide) for nanocrystalline dye-sensitized solar cells (2008) Electrochim. Acta, 53, pp. 7903-7907; Manikandan, P., Padmakumar, K., Justin Thomas, K.R., Varghese, B., Onodera, H., Manoharan, P.T., Lattice-Dictated Conformers in Bis(pyrazolyl)pyridine-Based Iron(II) Complexes: M�ssbauer, NMR, and Magnetic Studies (2001) Inorg. Chem., 40, pp. 6930-6939; Jameson, D.L., Goldsby, K.A., 2,6-bis(N-pyrazolyl)pyridines: The convenient synthesis of a family of planar tridentate N3 ligands that are terpyridine analogs (1990) J. Org. Chem., 55, pp. 4992-4994; Zoppellaro, G., Enkelmann, V., Geies, A., Baumgarten, M., A Multifunctional High-Spin Biradical Pyrazolylbipyridine-bisnitronylnitroxide (2004) Org. Lett., 6, pp. 4929-4932; Prakash, O., Hussain, K., Kumar, R., Wadhwa, D., Sharma, C., Aneja, K.R., Synthesis and antimicrobial evaluation of new1,4-dihydro-4-pyrazolylpyridines and 4-Pyrazolylpyridines (2011) Org. Med. Chem. Lett., 1, pp. 1-7; Motaung, M.P., Ajibade, P.A., Ru(II) and Co(II) Complexes of bis(pyrazolyl)pyridine and pyridine-2,6-dicarboxylic Acid: Synthesis, Photo Physical Studies and Evaluation of Solar Cell Conversion Efficiencies (2015) Int. J. Electrochem. Sci., 10, pp. 8087-8096; Zoppellaro, G., Geies, G., Enkelmann, V., Baumgarten, M., 2,6-Bis(pyrazolyl)pyridine Functionalised with Two Nitronylnitroxide and Iminonitroxide Radicals (2004) Eur. J. Org. Chem., 2004, pp. 2367-2374; Gomha, S.M., Salah, T.A., Abdelhamid, A.O., Synthesis, characterization and pharmacological evaluation of some novel thiadiazoles and thiazoles incorporating pyrazole moiety as potent anticancer agents (2015) Monatsh. Chem., 146, pp. 149-158; Gomha, S.M., Abdel-aziz, H.M., Synthesis and antitumor activity of 1,3,4-thiadiazole derivatives bearing coumarine ring (2015) Heterocycles, 91, pp. 583-592; Dawood, K.M., Gomha, S.M., Synthesis and anti-cancer activity of 1,3,4-thiadiazole and 1,3-thiazole derivatives having 1,3,4-oxadiazole moiety (2015) J. Heterocycl. Chem., 52, pp. 1400-1405; Abbas, I.M., Gomha, S.M., Elneairy, M.A.A., Elaasser, M.M., Mabrouk, B.K.A., Antimicrobial and anticancer evaluation of novel synthetic tetracyclic system through Dimroth rearrangement (2015) J. Serb. Chem. Soc., 80, pp. 1251-1264; Gomha, S.M., Abbas, I.M., Elneairy, M.A.A., Elaasser, M.M., Mabrouk, B.K.A., Synthesis and biological evaluation of novel fused triazolo[4,3-a] pyrimidinones (2015) Turk. J. Chem., 39, pp. 510-531; Gomha, S.M., Zaki, Y.H., Abdelhamid, A.O., Utility of 3-acetyl-6-bromo-2H-chromen-2-one for synthesis of new heterocycles as potential anticancer agents (2015) Molecules, 20, pp. 21826-21839; Gomha, S.M., Riyadh, S.M., Mahmmoud, E.A., Elaasser, M.M., Chitosan-grafted-poly(4-vinylpyridine) as a novel copolymer basic catalyst for synthesis of arylazothiazoles and 1,3,4-thiadiazoles under microwave irradiation (2015) Chem. Heterocycl. Comp., 51, pp. 1030-1038; Gomha, S.M., Salah, T.A., Hassaneen, H.M.E., Abdel-aziz, H., Khedr, M.A., Synthesis, characterization and molecular docking of novel bioactive thiazolyl-thiazole derivatives as promising cytotoxic antitumor drug (2016) Molecules, 21 (3); Gomha, S.M., Badrey, M.G., Edrees, M.M., Heterocyclization of a bis-thiosemicarbazone of 2,5-diacetyl-3,4-disubstituted-thieno[2,3-b]thiophene bis-thiosemicarbazones leading to bis-thiazoles and bis-1,3,4-thiadiazoles as anti-breast cancer agents (2016) J. Chem. Res., 40, pp. 120-125; Gomha, S.M., Abdallah, M.A., Mourad, M.A., Elaasser, M.M., Application of Mannich and Michael reactions in synthesis of pyridopyrimido[2,1-b][1,3,5]thiadiazinones and pyridopyrimido[2,1-b][1,3]thiazinones and their biological activity (2016) Heterocycles, (92), pp. 688-699; Ibrahim, M.K., El-Ghandour, A.H.H., Abou-hadeed, K., Abdelhafiz, I.S. Utility of hydzidoyl chlorides: Synthesis of new pyrazoles, pyrazolo[3,4-d]pyridazines, pyrazolo[4,5-b]pyridines and pyrazolo[4,5-d] pyrimidine derivatives (1992) J. Ind. Chem. Soc., 69, pp. 378-380; Gomha, S.M., Abdalla, M.A., Abdelaziz, M., Serag, N., Eco-friendly one-pot synthesis and antiviral evaluation of pyrazolyl chalcones and pyrazolines of medicinal interest (2016) Turk. J. Chem., 40, pp. 484-498; Shawali, A.S., Gomha, S.M., A new entry for short and regioselective synthesis of [1,2,4]triazolo[4,3-b][1,2,4]-triazin-7(1H)-one (2000) Adv. Synth. Catal., (342), pp. 599-604; Gomha, S.M., Riyadh, S.M., Abbas, I.M., Bauomi, M.A., Synthetic utility of ethylidenethiosemicarbazide: Synthesis and and anti-cancer activity of 1,3-thiazines and thiazoles with imidazole moiety (2012) Heterocycles, 87, pp. 341-356 |
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