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Volumn 34, Issue 4, 2014, Pages 1673-1678

Anticancer activity of novel pyrido[2,3-b] indolizine derivatives: The relevance of phenolic substituents

Author keywords

Cell cycle; Colorectal cancer; Cytotoxicity; HCT116; HT 29 and RKO cell lines; Indolizine derivatives

Indexed keywords

4 (3,4) DIHYDROXYPHENYL) 2 PHENYLPYRIDO[2,3B]INDOLIZINE 10 CARBONITRILE; ANTINEOPLASTIC AGENT; INDOLIZINE DERIVATIVE; UNCLASSIFIED DRUG; INDOLIZINE; PHENOL DERIVATIVE;

EID: 84902241819     PISSN: 02507005     EISSN: 17917530     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (17)

References (23)
  • 2
    • 79953272159 scopus 로고    scopus 로고
    • Genetics, cytogenetics, and epigenetics of colorectal cancer
    • Migliore L, Migheli F, Spisni R, and Coppede F: Genetics, cytogenetics, and epigenetics of colorectal cancer. J Biomed Biotechnol 2011: 792362, 2011.
    • (2011) J Biomed Biotechnol , vol.2011 , pp. 792362
    • Migliore, L.1    Migheli, F.2    Spisni, R.3    Coppede, F.4
  • 3
    • 0036175062 scopus 로고    scopus 로고
    • Emerging pathways in colorectal-cancer development
    • Haydon AM and Jass JR: Emerging pathways in colorectal-cancer development. Lancet Oncol 3: 83-88, 2002.
    • (2002) Lancet Oncol , vol.3 , pp. 83-88
    • Haydon, A.M.1    Jass, J.R.2
  • 5
    • 77949435827 scopus 로고    scopus 로고
    • Molecular mechanisms of resistance to cetuximab and panitumumab in colorectal cancer
    • Bardelli A and Siena S: Molecular mechanisms of resistance to cetuximab and panitumumab in colorectal cancer. J Clin Oncol 28: 1254-1261, 2010.
    • (2010) J Clin Oncol , vol.28 , pp. 1254-1261
    • Bardelli, A.1    Siena, S.2
  • 7
    • 77953725220 scopus 로고    scopus 로고
    • Targeted treatments in colorectal cancer: State of the art and future perspectives
    • Arnold D and Seufferlein T: Targeted treatments in colorectal cancer: state of the art and future perspectives. Gut 59: 838-858, 2010.
    • (2010) Gut , vol.59 , pp. 838-858
    • Arnold, D.1    Seufferlein, T.2
  • 9
    • 84880116104 scopus 로고    scopus 로고
    • Synthesis and biological evaluation of bis-imidazolidineiminothiones: A comparative study
    • El-Sharief MA, Moussa Z and El-Sharief AM: Synthesis and biological evaluation of bis-imidazolidineiminothiones: a comparative study. Arch Pharm (Weinheim) 346: 542-555, 2013.
    • (2013) Arch Pharm (Weinheim) , vol.346 , pp. 542-555
    • El-Sharief, M.A.1    Moussa, Z.2    El-Sharief, A.M.3
  • 10
    • 77954348728 scopus 로고    scopus 로고
    • Synthesis and antiproliferative activity of indolizine derivatives incorporating a cyclopropylcarbonyl group against Hep-G2 cancer cell line
    • Shen YM, Lv PC, Chen W, Liu PG, Zhang MZ and Zhu HL: Synthesis and antiproliferative activity of indolizine derivatives incorporating a cyclopropylcarbonyl group against Hep-G2 cancer cell line. Eur J Med Chem 45: 3184-3190, 2010.
    • (2010) Eur J Med Chem , vol.45 , pp. 3184-3190
    • Shen, Y.M.1    Lv, P.C.2    Chen, W.3    Liu, P.G.4    Zhang, M.Z.5    Zhu, H.L.6
  • 11
    • 40749158239 scopus 로고    scopus 로고
    • Indole- and indolizine-glyoxylamides displaying cytotoxicity against multidrug resistant cancer cell lines
    • James DA, Koya K, Li H, Liang G, Xia Z, Ying W, Wu Y and Sun L: Indole- and indolizine-glyoxylamides displaying cytotoxicity against multidrug resistant cancer cell lines. Bioorg Med Chem Lett 18: 1784-1787, 2008.
    • (2008) Bioorg Med Chem Lett , vol.18 , pp. 1784-1787
    • James, D.A.1    Koya, K.2    Li, H.3    Liang, G.4    Xia, Z.5    Ying, W.6    Wu, Y.7    Sun, L.8
  • 12
    • 0034607947 scopus 로고    scopus 로고
    • Sugar-mimic glycosidase inhibitors: Natural occurrence, biological activity and prospects for therapeutic application
    • Asano N, Nash RJ, Molyneux RJ and Fleet GWJ: Asano, N. Sugar-mimic glycosidase inhibitors: natural occurrence, biological activity and prospects for therapeutic application. Tetrahedron: Asymmetry 11: 1645-1680, 2000.
    • (2000) Tetrahedron: Asymmetry , vol.11 , pp. 1645-1680
    • Asano, N.1    Nash, R.J.2    Molyneux, R.J.3    Fleet, G.W.J.4    Asano, N.5
  • 13
    • 0031799484 scopus 로고    scopus 로고
    • Topical anti-inflammatory activity of new 2-(1-indolizinyl)propionic acid derivatives in mice
    • Malonne H, Hanuise J and Fontaine J: Topical anti-inflammatory activity of new 2-(1-indolizinyl)propionic acid derivatives in mice. Pharm Pharmacol Commun 4: 241-243, 1998.
    • (1998) Pharm Pharmacol Commun , vol.4 , pp. 241-243
    • Malonne, H.1    Hanuise, J.2    Fontaine, J.3
  • 14
    • 0031978292 scopus 로고    scopus 로고
    • Crystal structure of human secretory phospholipase A2-IIA complex with the potent indolizine inhibitor 120-1032
    • Kitadokoro K, Hagishita S, Sato T, Ohtani M and Miki K: Crystal structure of human secretory phospholipase A2-IIA complex with the potent indolizine inhibitor 120-1032. J Biochem 123: 619-623, 1998.
    • (1998) J Biochem , vol.123 , pp. 619-623
    • Kitadokoro, K.1    Hagishita, S.2    Sato, T.3    Ohtani, M.4    Miki, K.5
  • 16
    • 33845380273 scopus 로고    scopus 로고
    • Synthesis of indolizine derivatives with selective antibacterial activity against Mycobacterium tuberculosis
    • Gundersen LL, Charnock C, Negussie AH, Rise F, and Teklu S: Synthesis of indolizine derivatives with selective antibacterial activity against Mycobacterium tuberculosis. Eur J Pharm Sci 30: 26-35, 2007.
    • (2007) Eur J Pharm Sci , vol.30 , pp. 26-35
    • Gundersen, L.L.1    Charnock, C.2    Negussie, A.H.3    Rise, F.4    Teklu, S.5
  • 17
    • 84880699191 scopus 로고    scopus 로고
    • Design, synthesis and biological evaluation of indolizine derivatives as HIV-1 VIF-ElonginC interaction inhibitors
    • Huang W, Zuo T, Jin H, Liu Z, Yang Z, Yu X, Zhang L and Zhang L: Design, synthesis and biological evaluation of indolizine derivatives as HIV-1 VIF-ElonginC interaction inhibitors. Mol Divers 17: 221-243, 2013.
    • (2013) Mol Divers , vol.17 , pp. 221-243
    • Huang, W.1    Zuo, T.2    Jin, H.3    Liu, Z.4    Yang, Z.5    Yu, X.6    Zhang, L.7    Zhang, L.8
  • 18
    • 9144257874 scopus 로고    scopus 로고
    • Potent, selective and cell-mediated inhibition of human herpesvirus 6 at an early stage of viral replication by the non-nucleoside compound CMV423
    • de Bolle L, Andrei G, Snoeck R, Zhang Y, Van LA, Otto M, Bousseau A, Roy C, De CE and Naesens L: Potent, selective and cell-mediated inhibition of human herpesvirus 6 at an early stage of viral replication by the non-nucleoside compound CMV423. Biochem Pharmacol 67: 325-336, 2004.
    • (2004) Biochem Pharmacol , vol.67 , pp. 325-336
    • De Bolle, L.1    Andrei, G.2    Snoeck, R.3    Zhang, Y.4    Van, L.A.5    Otto, M.6    Bousseau, A.7    Roy, C.8    De, C.E.9    Naesens, L.10
  • 19
    • 0038268719 scopus 로고    scopus 로고
    • Phospholipid microspheres: A novel delivery mode for targeting antileishmanial agent in experimental leishmaniasis
    • Medda S, Jaisankar P, Manna RK, Pal B, Giri VS, and Basu MK: Phospholipid microspheres: a novel delivery mode for targeting antileishmanial agent in experimental leishmaniasis. J Drug Target 11: 123-128, 2003.
    • (2003) J Drug Target , vol.11 , pp. 123-128
    • Medda, S.1    Jaisankar, P.2    Manna, R.K.3    Pal, B.4    Giri, V.S.5    Basu, M.K.6
  • 20
    • 0036462605 scopus 로고    scopus 로고
    • Recent developments of transition-state analogue glycosidase inhibitors of non-natural product origin
    • Lillelund VH, Jensen HH, Liang X and Bols M: Recent developments of transition-state analogue glycosidase inhibitors of non-natural product origin. Chem Rev 102: 515-553, 2002.
    • (2002) Chem Rev , vol.102 , pp. 515-553
    • Lillelund, V.H.1    Jensen, H.H.2    Liang, X.3    Bols, M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.