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Volumn 16, Issue 2, 2005, Pages 145-150

Cytotoxicities of three rebeccamycin derivatives in the National Cancer Institute screening of 60 human tumor cell lines

Author keywords

COMPARE analysis; Cytotoxicity; DNA binding; Indolocarbazoles; Inhibition; Topoisomerase I

Indexed keywords

BMS 181176; CARBAZOLE DERIVATIVE; DNA TOPOISOMERASE; INDOLE DERIVATIVE; NSC 726576; NSC 726577; NSC 726578; POISON; REBECCAMYCIN;

EID: 13844267548     PISSN: 09594973     EISSN: None     Source Type: Journal    
DOI: 10.1097/00001813-200502000-00005     Document Type: Article
Times cited : (13)

References (18)
  • 1
    • 0032936474 scopus 로고    scopus 로고
    • Advances in indolo[2,3-a]carbazole chemistry: Design and synthesis of protein kinase C and topoisomerase I inhibitors
    • Pindur U, Kim Y-S, Mehrabani F. Advances in indolo[2,3-a]carbazole chemistry: design and synthesis of protein kinase C and topoisomerase I inhibitors. Curr Med Chem 1999; 6:29-69.
    • (1999) Curr Med Chem , vol.6 , pp. 29-69
    • Pindur, U.1    Kim, Y.-S.2    Mehrabani, F.3
  • 2
    • 0033755667 scopus 로고    scopus 로고
    • Recent developments of rebeccamycin analogues as topoisomerase I inhibitors and antitumor agents
    • Prudhomme M. Recent developments of rebeccamycin analogues as topoisomerase I inhibitors and antitumor agents. Curr Med Chem 2000; 7:1189-1212.
    • (2000) Curr Med Chem , vol.7 , pp. 1189-1212
    • Prudhomme, M.1
  • 3
    • 0002487727 scopus 로고    scopus 로고
    • Recent developments in the synthesis of indolocarbazoles, topoisomerase I inhibitors
    • Prudhomme M, Anizon F, Moreau P. Recent developments in the synthesis of indolocarbazoles, topoisomerase I inhibitors. Recent Res Dev Synth Organic Chem 1999; 2:79-106.
    • (1999) Recent Res Dev Synth Organic Chem , vol.2 , pp. 79-106
    • Prudhomme, M.1    Anizon, F.2    Moreau, P.3
  • 4
    • 0000714445 scopus 로고    scopus 로고
    • Structure-activity relationships in a series of substituted indolocarbazoles: Topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties
    • Rodrigues-Pereira E, Belin L, Sancelme M, Prudhomme M, Ollier M, Rapp M, et al. Structure-activity relationships in a series of substituted indolocarbazoles: topoisomerase I and protein kinase C inhibition and antitumoral and antimicrobial properties. J Med Chem 1996; 39:4471-4477.
    • (1996) J Med Chem , vol.39 , pp. 4471-4477
    • Rodrigues-Pereira, E.1    Belin, L.2    Sancelme, M.3    Prudhomme, M.4    Ollier, M.5    Rapp, M.6
  • 5
    • 0023178261 scopus 로고
    • Production and biological activity of rebeccamycin, a novel antitumor agent
    • Bush JA, Long JJ, Catino WT, Bradner K, Tomita K. Production and biological activity of rebeccamycin, a novel antitumor agent. J Antibiotics 1987; 40:668-678.
    • (1987) J Antibiotics , vol.40 , pp. 668-678
    • Bush, J.A.1    Long, J.J.2    Catino, W.T.3    Bradner, K.4    Tomita, K.5
  • 7
    • 9844260513 scopus 로고    scopus 로고
    • Syntheses and biological activities (Topoisomerase inhibition and antitumor and antimicrobial properties) of rebeccamycin analogues bearing modified sugar moieties and substituted on the imide nitrogen with a methyl group
    • Anizon F, Belin L, Moreau P, Sancelme M, Voldoire A, Prudhomme M, et al. Syntheses and biological activities (Topoisomerase inhibition and antitumor and antimicrobial properties) of rebeccamycin analogues bearing modified sugar moieties and substituted on the imide nitrogen with a methyl group. J Med Chem 1997; 40:3456-3465.
    • (1997) J Med Chem , vol.40 , pp. 3456-3465
    • Anizon, F.1    Belin, L.2    Moreau, P.3    Sancelme, M.4    Voldoire, A.5    Prudhomme, M.6
  • 8
    • 15144351325 scopus 로고    scopus 로고
    • Syntheses and biological evaluation of indolocarbazoles, analogues of rebeccamycin, modified at the imide heterocycle
    • Moreau P, Anizon F, Sancelme M, Prudhomme M, Bailly C, Carrasco C, et al. Syntheses and biological evaluation of indolocarbazoles, analogues of rebeccamycin, modified at the imide heterocycle. J Med Chem 1998; 41:1631-1640.
    • (1998) J Med Chem , vol.41 , pp. 1631-1640
    • Moreau, P.1    Anizon, F.2    Sancelme, M.3    Prudhomme, M.4    Bailly, C.5    Carrasco, C.6
  • 9
    • 0032168946 scopus 로고    scopus 로고
    • Syntheses, biochemical and biological evaluation of staurosporine analogues from microbial metabolite rebeccamycin
    • Anizon F, Moreau P, Sancelme M, Voldoire A, Prudhomme M, Ollier M, et al. Syntheses, biochemical and biological evaluation of staurosporine analogues from microbial metabolite rebeccamycin. Bioorg Med Chem 1998; 6:1597-1604.
    • (1998) Bioorg Med Chem , vol.6 , pp. 1597-1604
    • Anizon, F.1    Moreau, P.2    Sancelme, M.3    Voldoire, A.4    Prudhomme, M.5    Ollier, M.6
  • 10
    • 0042121548 scopus 로고    scopus 로고
    • Rebeccamycin analogues bearing amine substituents or other groups on the sugar moiety
    • Anizon F, Moreau P, Sancelme M, Laine W, Bailly C, Prudhomme M. Rebeccamycin analogues bearing amine substituents or other groups on the sugar moiety. Bioorg Med Chem 2003; 11:3709-3722.
    • (2003) Bioorg Med Chem , vol.11 , pp. 3709-3722
    • Anizon, F.1    Moreau, P.2    Sancelme, M.3    Laine, W.4    Bailly, C.5    Prudhomme, M.6
  • 11
    • 0242361216 scopus 로고    scopus 로고
    • Semi-synthesis, topoisomerase I and kinases inhibitory properties, and antiproliferative activities of new rebeccamycin derivatives
    • Moreau P, Gaillard N, Marminon C, Anizon F, Dias N, Baldeyrou B, et al. Semi-synthesis, topoisomerase I and kinases inhibitory properties, and antiproliferative activities of new rebeccamycin derivatives. Bioorg Med Chem 2003; 11:4871-4879.
    • (2003) Bioorg Med Chem , vol.11 , pp. 4871-4879
    • Moreau, P.1    Gaillard, N.2    Marminon, C.3    Anizon, F.4    Dias, N.5    Baldeyrou, B.6
  • 12
    • 0033602140 scopus 로고    scopus 로고
    • Syntheses and biological activities of rebeccamycin analogues. Introduction of a halogenoacetyl substituent
    • Moreau P, Anizon F, Sancelme M, Prudhomme M, Bailly C, Severe D, et al. Syntheses and biological activities of rebeccamycin analogues. Introduction of a halogenoacetyl substituent. J Med Chem. 1999; 42:584-592.
    • (1999) J Med Chem , vol.42 , pp. 584-592
    • Moreau, P.1    Anizon, F.2    Sancelme, M.3    Prudhomme, M.4    Bailly, C.5    Severe, D.6
  • 13
    • 0033587125 scopus 로고    scopus 로고
    • Synthesis, mode of action, and biological activities of rebeccamycin bromoderivatives
    • Moreau P, Anizon F, Sancelme M, Prudhomme M, Sevėre D, Riou J-F, et al. Synthesis, mode of action, and biological activities of rebeccamycin bromoderivatives. J Med Chem 1999; 42:1816-1822.
    • (1999) J Med Chem , vol.42 , pp. 1816-1822
    • Moreau, P.1    Anizon, F.2    Sancelme, M.3    Prudhomme, M.4    Severe, D.5    Riou, J.-F.6
  • 14
    • 0344809977 scopus 로고    scopus 로고
    • ATP-site directed inhibitors of cyclin-dependent kinases
    • Gray N, Dėtivaud L, Doerig C, Meijer L. ATP-site directed inhibitors of cyclin-dependent kinases. Curr Med Chem. 1999; 6:859-875.
    • (1999) Curr Med Chem , vol.6 , pp. 859-875
    • Gray, N.1    Detivaud, L.2    Doerig, C.3    Meijer, L.4
  • 15
    • 0035672148 scopus 로고    scopus 로고
    • Synthesis and biological activities of indolocarbazoles bearing amino acid residues
    • Moreau P, Sancelme M, Bailly C, Léonce S, Pierré A, Hickman J, et al. Synthesis and biological activities of indolocarbazoles bearing amino acid residues. Eur J Med Chem 2001; 36:887-897.
    • (2001) Eur J Med Chem , vol.36 , pp. 887-897
    • Moreau, P.1    Sancelme, M.2    Bailly, C.3    Léonce, S.4    Pierré, A.5    Hickman, J.6
  • 16
    • 0025775062 scopus 로고
    • Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human tumor cell lines
    • Monks A, Scudiero D, Skehan P, Shoemaker R, Paull K, Vistica D, et al. Feasibility of a high-flux anticancer drug screen using a diverse panel of cultured human tumor cell lines. J Nat Cancer Inst 1991; 83:757-766.
    • (1991) J Nat Cancer Inst , vol.83 , pp. 757-766
    • Monks, A.1    Scudiero, D.2    Skehan, P.3    Shoemaker, R.4    Paull, K.5    Vistica, D.6
  • 18
    • 0024312538 scopus 로고
    • Display and analysis of patterns of differential activity of drugs against human tumor cell lines: Development of mean graph and COMPARE algorithm
    • Paull KD, Shoemaker RH, Hodes L, Monks A, Scudiero DA, Rubinstein L, et al. Display and analysis of patterns of differential activity of drugs against human tumor cell lines: development of mean graph and COMPARE algorithm. J Natl Cancer Inst 1989; 81:1088-1092.
    • (1989) J Natl Cancer Inst , vol.81 , pp. 1088-1092
    • Paull, K.D.1    Shoemaker, R.H.2    Hodes, L.3    Monks, A.4    Scudiero, D.A.5    Rubinstein, L.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.