Synthesis and in vitro antitumor activity of some new Mannich bases

dc.AffiliationOctober University for modern sciences and Arts (MSA)
dc.contributor.authorKandeel M.M.
dc.contributor.authorAbdou N.A.
dc.contributor.authorKadry H.H.
dc.contributor.authorEl-Masry R.M.
dc.contributor.otherPharmaceutical Organic Chemistry Department
dc.contributor.otherFaculty of Pharmacy
dc.contributor.otherCairo University
dc.contributor.otherCairo
dc.contributor.other11562
dc.contributor.otherEgypt; Organic Chemistry Department
dc.contributor.otherOctober University for Modern Sciences and Arts
dc.contributor.other6 October City
dc.contributor.otherEgypt
dc.date.accessioned2020-01-09T20:42:29Z
dc.date.available2020-01-09T20:42:29Z
dc.date.issued2013
dc.descriptionScopus
dc.description.abstractTwo series of Novel Mannich bases has been synthesized from chalcones 3 and 7 and evaluated for their in vitro cytotoxic activity. Out of the newly synthesized compounds, four derivatives 4a, 4b, 4e, 4f were selected by the National Cancer Institute (NCI) to be evaluated for their in-vitro antitumor activity by in-vitro disease-oriented human cells screening panel assay. All the tested compounds exhibited a broad spectrum of antitumor activity against renal cancer UO-31.en_US
dc.description.urihttps://www.scimagojr.com/journalsearch.php?q=19700175055&tip=sid&clean=0
dc.identifier.doihttps://doi.org/
dc.identifier.issn9744290
dc.identifier.otherhttps://doi.org/
dc.identifier.urihttps://t.ly/2dwYb
dc.language.isoEnglishen_US
dc.relation.ispartofseriesInternational Journal of ChemTech Research
dc.relation.ispartofseries5
dc.subjectAntitumor activityen_US
dc.subjectChalconesen_US
dc.subjectCytotoxicityen_US
dc.subjectMannich basesen_US
dc.subjectSynthesisen_US
dc.subjectantineoplastic agenten_US
dc.subjectchalcone derivativeen_US
dc.subjectMannich baseen_US
dc.subjectantineoplastic activityen_US
dc.subjectarticleen_US
dc.subjectcell counten_US
dc.subjectcolon canceren_US
dc.subjectcontrolled studyen_US
dc.subjectcytotoxicityen_US
dc.subjectdrug synthesisen_US
dc.subjectgrowth inhibitionen_US
dc.subjecthumanen_US
dc.subjecthuman cellen_US
dc.subjectinfrared spectrophotometryen_US
dc.subjectkidney canceren_US
dc.subjectmass fragmentographyen_US
dc.subjectmelting pointen_US
dc.subjectmicroanalysisen_US
dc.subjectproton nuclear magnetic resonanceen_US
dc.subjectthin layer chromatographyen_US
dc.titleSynthesis and in vitro antitumor activity of some new Mannich basesen_US
dc.typeArticleen_US
dcterms.isReferencedByDimmock, J.R., Kandepu, N.M., Hetherington, M., Quail, J.W., Pugazhenthi, U., Sudom, A.M., Chamankhah, M., Balzarini, J., Cytotoxic Activities of Mannich Bases of Chalcones and Related Compounds (1998) J. Med. Chem, 41, pp. 1014-1026; Gul, H.I., Yerdelen, K.O., Gul, M., Das, U., Pandit, B., Li, P.K., Secen, H., Sahin, F., Synthesis of 4'-Hydroxy-3'- piperidinomethylchalcone derivatives and their cytotoxicity against PC-3 cell lines (2007) Arch. Pharm. Chem. Life Sci, 340, pp. 195-201; Gul, H.I., Yerdelen, K.O., Das, U., Gul, M., Pandit, B., Li, P.K., Dimmock, J.R., Synthesis and Cytotoxicity of Novel 3-Aryl-1-(3'- dibenzylaminomethyl-4'-hydroxyphenyl)- propenones and Related Compounds (2008) Chem. Pharm. Bull, 56, pp. 1675-1681; Hieu, B.T., Thuy, L.T., Thuy, V.T., Tien, H.X., Chinh, L.V., Hoang, V.D., Vu, T.K., Design, Synthesis and In Vitro Cytotoxic Activity Evaluation of New Mannich Bases (2012) Bull Korean Chem Soc, 33, pp. 1586-1592; Reddy, M.V.B., Sua, C.R., Chioub, W.F., Liuc, Y.N., Chenc, R.Y.H., Bastowc, K.F., Leec, K.H., Wua, T.S., Design, synthesis, and biological evaluation of Mannich bases of heterocyclic chalcone analogs as cytotoxic agents (2008) Bioorg & Med. Chem, 16, pp. 7358-7370; Hua, G., Wang, G., Duana, N., Wena, X., Caoa, T., Xiea, S., Huangb, W., Design, synthesis and antitumor activities of fluoroquinolone C-3 heterocycles (IV): S-triazole Schiff-Mannich bases derived from ofloxacin (2012) Acta Pharmaceutica Sinica B, 2, pp. 312-317; Shawa, A.Y., Changa, C.Y., Hsua, M.Y., Lub, P.J., Yangc, C.N., Chenb, H.L., Loc, C.W., Cherna, M.K., Synthesis and structure-activity relationship study of 8- hydroxyquinoline-derived Mannich bases as anticancer agents (2010) Eur. J. Med. Chem, 45, pp. 2860-2867; Reddy, M.V.B., Shen, Y.C., Yang, J.S., Hwang, T.L., Bastow, K.F., Qian, K., Lee, K.H., Wua, T.S., New bichalcone analogs as NF-jB inhibitors and as cytotoxic agents inducing Fas/CD95-dependent apoptosis (2011) Bioorg & Med. Chem, 19, pp. 1895-1906; Dimmock, J.R., Advikolanu, K.M., Scott, H.E., Duffy, M.J., Reid, R.S., Quail, J.W., Jia, Z., Rutledge, J.M., Evaluation of cytotoxicity of some Mannich bases of various aryl and arylidene ketones and their corresponding arylhydrazones (1992) J. Pharm. Sci, 81, pp. 1147-1152; Dimmock, J.R., Kumar, P., Anticancer and Cytotoxic Properties of Mannich Bases (1997) Curr. Med. Chem, 4, pp. 1-22; Kumar, D., Kumar, N.M., Akamatsu, K., Kusaka, E., Harada, H., Ito, T., Synthesis and biological evaluation of indolyl chalcones as antitumor agents (2010) Bioorg & Med. Chem. Lett, 20, pp. 3916-3919; Bamnela, R., Shrivastava, S.P., Synthesis and Biological Activity of 4, 6-Substituted aryl-1-acetyl pyrimidine-2-ols (2010) Asian J. Chem, 22, pp. 6553-6558; Grever, M.R., Schepartz, S.A., Chabner, B.A., The National Cancer Institute: Cancer drug discovery and development program (1992) Semin. Oncol, 19, pp. 622-638; Monks, A., Scudiero, D., Skehan, P., Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human tumor cell lines (1991) J. Natl. Cancer Inst, 83, pp. 757-766; Boyd, M.R., Paull, K.D., Some practical considerations and applications of the national cancer institute in vitro anticancer drug discovery screen (1995) Drug Dev. Res, 34, pp. 91-109; Skehan, P., Storeng, R., Scudiero, D., Monks, A., McMahon, J., Vistica, D., Warren, J.R., Boyd, M.R., New colorimetric cytotoxic assay for anticancer drug screening (1990) J. Natl. Cancer Inst, 82, pp. 1107-1112
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