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Volumn 20, Issue 5, 2011, Pages 615-625

Design, synthesis, and QSAR study of novel 2-(2,3-dioxo-2,3- dihydro-1H-indol-1-yl)-N-phenylacetamide derivatives as cytotoxic agents

Author keywords

Cytotoxic assay; Isatin; QSAR; XTT assay

Indexed keywords

2 (5,7 DIBROMO 2,3 DIOXO 2,3 DIHYDRO 1H INDOL 1 YL) N (4 NITROPHENYL)ACETAMIDE; 5,7 DIBROMOISATIN; ACETANILIDE; CYTOTOXIC AGENT; ISATIN; UNCLASSIFIED DRUG; VINBLASTINE;

EID: 80052022639     PISSN: 10542523     EISSN: 15548120     Source Type: Journal    
DOI: 10.1007/s00044-010-9361-y     Document Type: Article
Times cited : (30)

References (26)
  • 1
    • 33645981950 scopus 로고    scopus 로고
    • Synthesis of 3-substituted-2-oxoindole analogues and their evaluation as kinase inhibitors, anticancer and antiangiogenic agents
    • Abadi AH, Abou-Seri SM, Abdel-Rahman DE, Klein C, Lozach O, Meijer L (2006) Synthesis of 3-substituted-2-oxoindole analogues and their evaluation as kinase inhibitors, anticancer and antiangiogenic agents. Eur J Med Chem 41:296-305
    • (2006) Eur J Med Chem , vol.41 , pp. 296-305
    • Abadi, A.H.1    Abou-Seri, S.M.2    Abdel-Rahman, D.E.3    Klein, C.4    Lozach, O.5    Meijer, L.6
  • 3
    • 0035133804 scopus 로고    scopus 로고
    • D-24851, a novel synthetic microtubule inhibitor, exerts curative antitumoral activity in vivo, shows efficacy toward multidrug-resistant tumor cells, and lacks neurotoxicity
    • Bacher G, Nickel B, Emig P, Vanhoefer U, Seeber S, Shandra A, Klenner T, Beckers T (2001) D-24851, a novel synthetic microtubule inhibitor, exerts curative antitumoral activity in vivo, shows efficacy toward multidrug-resistant tumor cells, and lacks neurotoxicity. Cancer Res 61:392-399 (Pubitemid 32106651)
    • (2001) Cancer Research , vol.61 , Issue.1 , pp. 392-399
    • Bacher, G.1    Nickel, B.2    Emig, P.3    Vanhoefer, U.4    Seeber, S.5    Shandra, A.6    Klenner, T.7    Beckers, T.8
  • 6
    • 18044378037 scopus 로고    scopus 로고
    • A-432411, a novel indolinone compound that disrupts spindle pole formation and inhibits human cancer cell growth
    • DOI 10.1158/1535-7163.MCT-04-0229
    • Chen Z, Merta PJ, Lin NH, Tahir SK, Kovar P, Sham HL, Zhang H. (2005) A-432411, a novel indolinone compound that disrupts spindle pole formation and inhibits human cancer cell growth. Mol Cancer Ther 4:562-568 (Pubitemid 40601837)
    • (2005) Molecular Cancer Therapeutics , vol.4 , Issue.4 , pp. 562-568
    • Chen, Z.1    Merta, P.J.2    Lin, N.-H.3    Tahir, S.K.4    Kovar, P.5    Sham, H.L.6    Zhang, H.7
  • 7
    • 38749095499 scopus 로고    scopus 로고
    • Regioselective synthesis and antitumor screening of some novel N-phenylpyrazole derivatives
    • DOI 10.1016/j.bmc.2007.10.015, PII S0968089607008814
    • Farag AM, Mayhoub AS, Barakat SE, Bayomi AH (2008) Regioselective synthesis and antitumor screening of some novel Nphenylpyrazole derivatives. Bioorganic Med Chem 16:881-889 (Pubitemid 351175638)
    • (2008) Bioorganic and Medicinal Chemistry , vol.16 , Issue.2 , pp. 881-889
    • Farag, A.M.1    Mayhoub, A.S.2    Barakat, S.E.3    Bayomi, A.H.4
  • 10
    • 42149182035 scopus 로고    scopus 로고
    • Synthesis of 1-substituted 3-pyridinylmethylidenylindolin-2-ones and 1-substituted 3-quinolinylmethylidenylindolin-2-ones as the enhancers of ATRA-induced differentiation in HL-60 cells
    • DOI 10.1016/j.bmc.2008.02.093, PII S096808960800206X
    • Hung CY, Hsu MH, Huang LJ, Hwang CS, Lee O, Wu CY, Chen CH, Kuo SC (2008) Synthesis of 1-substituted 3-pyridinylmethylidenylindolin- 2-ones and 1-substituted 3-quinolinylmethylidenylindolin- 2-ones as the enhancers of ATRA-induced differentiation in HL-60 cells. Bioorganic Med Chem 16:4222-4232 (Pubitemid 351539054)
    • (2008) Bioorganic and Medicinal Chemistry , vol.16 , Issue.8 , pp. 4222-4232
    • Hung, C.-Y.1    Hsu, M.-H.2    Huang, L.-J.3    Hwang, C.-S.4    Lee, O.5    Wu, C.-Y.6    Chen, C.-H.7    Kuo, S.-C.8
  • 11
    • 0001269899 scopus 로고
    • Preparation of certain brominated cinchophens
    • Lindwall HG, Bandes J, Weinberg I (1931) Preparation of certain brominated cinchophens. J Am Chem Soc 53:317-319
    • (1931) J Am Chem Soc , vol.53 , pp. 317-319
    • Lindwall, H.G.1    Bandes, J.2    Weinberg, I.3
  • 13
    • 34447280628 scopus 로고    scopus 로고
    • Effect of formaldehyde and resveratrol on the viability of Vero, HepG2 and MCF-7 cells
    • DOI 10.1016/j.cellbi.2007.01.039, PII S1065699507001199
    • Marcsek ZL, Kocsis Z, Szende B, Tompa A (2007) Effect of formaldehyde and resveratrol on the viability of Vero, HepG2 and MCF-7 cells. Cell Biol Int 31:1214-1219 (Pubitemid 47044855)
    • (2007) Cell Biology International , vol.31 , Issue.10 , pp. 1214-1219
    • Marcsek, Z.L.1    Kocsis, Zs.2    Szende, B.3    Tompa, A.4
  • 17
    • 0032822045 scopus 로고    scopus 로고
    • Synthesis, antibacterial, antifungal and anti-HIV activities of Schiff and Mannich bases derived from isatin derivatives and N-[4-(4'-chlorophenyl) thiazol-2-yl] thiosemicarbazide
    • DOI 10.1016/S0928-0987(99)00038-X, PII S092809879900038X
    • Pandeya SN, Sriram D, Nath G, DeClercq E (1999) Synthesis, antibacterial, antifungal and anti-HIV activities of Schiff and Mannich bases derived from isatin derivatives and N-[4-(4- chlorophenyl) thiazol-2-yl] thiosemicarbazide. Eur J Pharm Sci 9:25-31 (Pubitemid 29430189)
    • (1999) European Journal of Pharmaceutical Sciences , vol.9 , Issue.1 , pp. 25-31
    • Pandeya, S.N.1    Sriram, D.2    Nath, G.3    Declercq, E.4
  • 19
    • 52949129170 scopus 로고    scopus 로고
    • QSAR study of 1,3-dioxo-4-methyl-2,3-dihydro-1h-pyrrolo [3,4-c] quinolines as caspase-3 inhibitors
    • Sharma S, Sahu K, Jain P, Mourya VK, Agrawal RK (2008) QSAR study of 1,3-dioxo-4-methyl-2,3-dihydro-1h-pyrrolo [3,4-c] quinolines as caspase-3 inhibitors. Med Chem Res 17:399-411
    • (2008) Med Chem Res , vol.17 , pp. 399-411
    • Sharma, S.1    Sahu, K.2    Jain, P.3    Mourya, V.K.4    Agrawal, R.K.5
  • 20
    • 65349195105 scopus 로고    scopus 로고
    • Discovery of substituted N -(2-oxoindolin-3-ylidene) benzohydrazides as new apoptosis inducers using a cell-and caspase-based HTS assay
    • Sirisoma N, Pervin A, Drewe J, Tseng B, Cai SX (2009) Discovery of substituted N -(2-oxoindolin-3-ylidene) benzohydrazides as new apoptosis inducers using a cell-and caspase-based HTS assay. Bioorganic Med Chem Lett 19:2710-2713
    • (2009) Bioorganic Med Chem Lett , vol.19 , pp. 2710-2713
    • Sirisoma, N.1    Pervin, A.2    Drewe, J.3    Tseng, B.4    Cai, S.X.5
  • 22
    • 73949084441 scopus 로고    scopus 로고
    • Hybrid pharmacophore design and synthesis of isatin-benzothiazole analogs for their anti-breast cancer activity
    • Solomon VR, Hu C, Lee H (2009) Hybrid pharmacophore design and synthesis of isatin-benzothiazole analogs for their anti-breast cancer activity. Bioorganic Med Chem 17:7585-7592
    • (2009) Bioorganic Med Chem , vol.17 , pp. 7585-7592
    • Solomon, V.R.1    Hu, C.2    Lee, H.3
  • 23
    • 4644360018 scopus 로고    scopus 로고
    • Application of a catalytic palladium biaryl synthesis reaction, via C-H functionalization, to the total synthesis of Amaryllidaceae alkaloids
    • DOI 10.1016/j.tet.2004.08.030, PII S0040402004013481
    • Torres JC, Pinto AC, Garden SJ (2004) Application of a catalytic palladium biaryl synthesis reaction, via C-H functionalization, to the total synthesis of Amaryllidaceae alkaloids. Tetrahedron 60:9889-9900 (Pubitemid 39296778)
    • (2004) Tetrahedron , vol.60 , Issue.44 , pp. 9889-9900
    • Torres, J.C.1    Pinto, A.C.2    Garden, S.J.3
  • 25
    • 35348823755 scopus 로고    scopus 로고
    • An investigation into the cytotoxicity and mode of action of some novel N-alkyl-substituted isatins
    • DOI 10.1021/jm0704189
    • Vine KL, Locke JM, Ranson M, Pyne SG, Bremner JB (2007a) An Investigation into the cytotoxicity and mode of action of some novel N-alkyl-substituted isatins. J Med Chem 50:5109-5117 (Pubitemid 47585708)
    • (2007) Journal of Medicinal Chemistry , vol.50 , Issue.21 , pp. 5109-5117
    • Vine, K.L.1    Locke, J.M.2    Ranson, M.3    Pyne, S.G.4    Bremner, J.B.5
  • 26
    • 33845324541 scopus 로고    scopus 로고
    • In vitro cytotoxicity evaluation of some substituted isatin derivatives
    • DOI 10.1016/j.bmc.2006.10.035, PII S0968089606008686
    • Vine KL, Locke JM, Ranson M, Pyne SG, Bremner JB (2007b) In vitro cytotoxicity evaluation of some substituted isatin derivatives. Bioorganic Med Chem 15:931-938 (Pubitemid 44880712)
    • (2007) Bioorganic and Medicinal Chemistry , vol.15 , Issue.2 , pp. 931-938
    • Vine, K.L.1    Locke, J.M.2    Ranson, M.3    Pyne, S.G.4    Bremner, J.B.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.