메뉴 건너뛰기




Volumn 63, Issue 1, 2005, Pages 35-43

Acronycine revisited: Development of benzo[b]acronycine antitumor agents;De l'acronycine aux dérivés de la benzo[b]acronycine: Conception et développement d'une nouvelle série d'antitumoraux

Author keywords

Acronycine; Alkylating agent; Antitumor activity; S23906; Sarcomelicope

Indexed keywords

1,2 DIACETOXY 1,2 DIHYDROBENZ[B]ACRONYCINE; 1,2 DIHYDROXY 1,2 DIHYDROACRONYCINE; ACRONINE; ANTINEOPLASTIC AGENT; BENZ[B]ACRONYCINE; S 239061; UNCLASSIFIED DRUG;

EID: 14244265661     PISSN: 00034509     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0003-4509(05)82249-7     Document Type: Article
Times cited : (15)

References (26)
  • 1
    • 33751062476 scopus 로고
    • Alkaloids of the Australian Rutaceae
    • Hughes GK, Lahey FN, Price JR. Alkaloids of the Australian Rutaceae. Nature 1948; 162: 223-4.
    • (1948) Nature , vol.162 , pp. 223-224
    • Hughes, G.K.1    Lahey, F.N.2    Price, J.R.3
  • 2
    • 84971074351 scopus 로고
    • A revision of the genus Sarcomelicope (Rutaceae)
    • Hartley TG. A revision of the genus Sarcomelicope (Rutaceae). Aust J Bot 1982; 30: 359-72.
    • (1982) Aust J Bot , vol.30 , pp. 359-372
    • Hartley, T.G.1
  • 5
    • 0001139190 scopus 로고
    • Alkaloids of Acronichia baueri - Extraction of the alkaloids and structure - Activity relationships
    • Svoboda GH. Alkaloids of Acronichia baueri - Extraction of the alkaloids and structure - activity relationships. Lloydia 1966; 29: 206-24.
    • (1966) Lloydia , vol.29 , pp. 206-224
    • Svoboda, G.H.1
  • 6
    • 0013937331 scopus 로고
    • Alkaloids of Acronychia baueri - Isolation of the alkaloids and study of the antitumor and other biological properties of acronycine
    • Svoboda GH, Poore GA, Simpson PJ, Boder GB. Alkaloids of Acronychia baueri - Isolation of the alkaloids and study of the antitumor and other biological properties of acronycine. J Pharm Sci 1966; 55: 758-68.
    • (1966) J Pharm Sci , vol.55 , pp. 758-768
    • Svoboda, G.H.1    Poore, G.A.2    Simpson, P.J.3    Boder, G.B.4
  • 7
    • 0020696419 scopus 로고
    • Phase I-II evaluation of acronycine in patients with multiple myeloma
    • Scarffe JH, Beaumont AR, Crowther D. Phase I-II evaluation of acronycine in patients with multiple myeloma. Cancer Treat Rep 1983; 67: 93-4.
    • (1983) Cancer Treat Rep , vol.67 , pp. 93-94
    • Scarffe, J.H.1    Beaumont, A.R.2    Crowther, D.3
  • 8
    • 0036024723 scopus 로고    scopus 로고
    • Structure-activity relationships in the acronycine series
    • Michel S, Tillequin F, Seguin E. Structure-activity relationships in the acronycine series. Curr Med Chem 2002; 9: 1241-53.
    • (2002) Curr Med Chem , vol.9 , pp. 1241-1253
    • Michel, S.1    Tillequin, F.2    Seguin, E.3
  • 9
    • 0015305826 scopus 로고
    • Synthesis and biological activity of acronycine analogs
    • Schneider J, Evans EL, Grunberg E, Fryer RI. Synthesis and biological activity of acronycine analogs. J Med Chem 1972; 15: 266-70.
    • (1972) J Med Chem , vol.15 , pp. 266-270
    • Schneider, J.1    Evans, E.L.2    Grunberg, E.3    Fryer, R.I.4
  • 11
    • 77957214926 scopus 로고
    • How anti-juvenile hormones work
    • Bowers SW. How anti-juvenile hormones work. Amer Zool 1981; 21: 737-42.
    • (1981) Amer Zool , vol.21 , pp. 737-742
    • Bowers, S.W.1
  • 12
    • 0030464450 scopus 로고    scopus 로고
    • Synthesis and cytotoxic and antitumor activity of esters in the 1,2-dihydroxy-1,2-dihydroacronycine series
    • Elomri A, Mitaku S, Michel S, Skaltsounis AL, Tillequin F, Koch M, et al. Synthesis and cytotoxic and antitumor activity of esters in the 1,2-dihydroxy-1,2-dihydroacronycine series. J Med Chem 1996; 39: 4762-6.
    • (1996) J Med Chem , vol.39 , pp. 4762-4766
    • Elomri, A.1    Mitaku, S.2    Michel, S.3    Skaltsounis, A.L.4    Tillequin, F.5    Koch, M.6
  • 13
    • 0031929359 scopus 로고    scopus 로고
    • Synthesis and biological activity of esters in the trans-1,2-dihydroxy-1, 2-dihydroacronycine series
    • Magiatis P, Mitaku S, Skaltsounis AL, Tillequin F, Koch M, Pierré A. Synthesis and biological activity of esters in the trans-1,2-dihydroxy-1,2- dihydroacronycine series. J Nat Prod 1998; 61: 198-201.
    • (1998) J Nat Prod , vol.61 , pp. 198-201
    • Magiatis, P.1    Mitaku, S.2    Skaltsounis, A.L.3    Tillequin, F.4    Koch, M.5    Pierré, A.6
  • 14
    • 0032916316 scopus 로고    scopus 로고
    • Chiral dihydroxylation of acronycine: Absolute configuration of natural cis-1,2-dihydroxy-1,2-dihydroacronycine and cytotoxicity of (1R, 2R)- and (1S, 2S)-1,2-diacetoxy-1,2-dihydroacronycine
    • Costes N, Michel S, Tillequin F, Koch M, Pierré A, Atassi Gh. Chiral dihydroxylation of acronycine: absolute configuration of natural cis-1,2-dihydroxy-1,2-dihydroacronycine and cytotoxicity of (1R, 2R)- and (1S, 2S)-1,2-diacetoxy-1,2-dihydroacronycine. J Nat Prod 1999; 62: 490-2.
    • (1999) J Nat Prod , vol.62 , pp. 490-492
    • Costes, N.1    Michel, S.2    Tillequin, F.3    Koch, M.4    Pierré, A.5    Atassi, Gh.6
  • 15
    • 0023795194 scopus 로고
    • Development of a parenteral formulation of the antitumour agent acronycine
    • Dorr RT, Liddil JD. Development of a parenteral formulation of the antitumour agent acronycine. J Drug Dev 1988; 1: 31-9.
    • (1988) J Drug Dev , vol.1 , pp. 31-39
    • Dorr, R.T.1    Liddil, J.D.2
  • 16
    • 0033945548 scopus 로고    scopus 로고
    • Synthesis and cytotoxic and antitumor activity of benzo[b]pyrano[3,2-h] acridine-7-one analogues of acronycine
    • Costes N, Le Deit H, Michel S, Tillequin F, Koch M, Pfeiffer B, et al. Synthesis and cytotoxic and antitumor activity of benzo[b]pyrano[3,2-h]acridine- 7-one analogues of acronycine. J Med Chem 2000; 43: 2395-402.
    • (2000) J Med Chem , vol.43 , pp. 2395-2402
    • Costes, N.1    Le Deit, H.2    Michel, S.3    Tillequin, F.4    Koch, M.5    Pfeiffer, B.6
  • 17
    • 0037698962 scopus 로고    scopus 로고
    • Structure-activity relationships and mechanism of action of antitumor benzo[b]pyrano [3,2-h]acridine-7-one acronycine analogues
    • Doan Thi Mai H, Gaslonde T, Michel S, Tillequin F, Koch M, Bongui JB, et al. Structure-Activity relationships and mechanism of action of antitumor benzo[b]pyrano [3,2-h]acridine-7-one acronycine analogues. J Med Chem 2003; 46: 3072-82.
    • (2003) J Med Chem , vol.46 , pp. 3072-3082
    • Doan Thi Mai, H.1    Gaslonde, T.2    Michel, S.3    Tillequin, F.4    Koch, M.5    Bongui, J.B.6
  • 18
    • 3242749631 scopus 로고    scopus 로고
    • Synthesis and cytotoxic and antitumor activity of 1,2-dihydroxy-1,2- dihydrobenzo[b] acronycine diacid hemiesters and carbamates
    • Doan Thi Mai H, Gaslonde T, Michel S, Koch M, Tillequin F, Pfeiffer B, et al. Synthesis and cytotoxic and antitumor activity of 1,2-dihydroxy-1,2- dihydrobenzo[b] acronycine diacid hemiesters and carbamates. Chem Pharm Bull 2004; 52: 293-7.
    • (2004) Chem Pharm Bull , vol.52 , pp. 293-297
    • Doan Thi Mai, H.1    Gaslonde, T.2    Michel, S.3    Koch, M.4    Tillequin, F.5    Pfeiffer, B.6
  • 23
    • 0035213896 scopus 로고    scopus 로고
    • Induction of cyclin E and inhibition of DNA synthesis by the novel acronycine derivative S23906-1 precede the irreversible arrest of the tumor cells in S phase leading to apoptosis
    • Léonce S, Perez V, Lambel S, Peyroulan D, Tillequin F, Michel S, Koch M, Pfeiffer B, Atassi Gh, Hickman J, Pierré A. Induction of cyclin E and inhibition of DNA synthesis by the novel acronycine derivative S23906-1 precede the irreversible arrest of the tumor cells in S phase leading to apoptosis. Mol Pharmacol 2001; 60: 1383-91.
    • (2001) Mol Pharmacol , vol.60 , pp. 1383-1391
    • Léonce, S.1    Perez, V.2    Lambel, S.3    Peyroulan, D.4    Tillequin, F.5    Michel, S.6    Koch, M.7    Pfeiffer, B.8    Atassi, Gh.9    Hickman, J.10    Pierré, A.11
  • 24
    • 0037090938 scopus 로고    scopus 로고
    • Induction of apoptosis in HL-60 leukemia and B16 melanoma cells by the acronycine derivative S23906-1
    • Kluza J, Lansiaux A, Wattez N, Hildebrand MP, Léonce S, Pierré A et al. Induction of apoptosis in HL-60 leukemia and B16 melanoma cells by the acronycine derivative S23906-1. Biochem Pharmacol 2002; 63: 1443-52.
    • (2002) Biochem Pharmacol , vol.63 , pp. 1443-1452
    • Kluza, J.1    Lansiaux, A.2    Wattez, N.3    Hildebrand, M.P.4    Léonce, S.5    Pierré, A.6
  • 25
    • 0037031292 scopus 로고    scopus 로고
    • Alkylation of guanine in DNA by S23906-1, a novel potent antitumor compound derived from the plant alkaloid acronycine
    • David-Cordonnier MH, Laine W, Lansiaux A, Kouach M, Briand G, Pierré A et al. Alkylation of guanine in DNA by S23906-1, a novel potent antitumor compound derived from the plant alkaloid acronycine. Biochemistry 2002; 41: 9911-20.
    • (2002) Biochemistry , vol.41 , pp. 9911-9920
    • David-Cordonnier, M.H.1    Laine, W.2    Lansiaux, A.3    Kouach, M.4    Briand, G.5    Pierré, A.6
  • 26
    • 0347301864 scopus 로고    scopus 로고
    • A transesterification reaction is implicated in the covalent binding of benzo[blacronycine anticancer agents with DNA and glutathione
    • David-Cordonnier MH, Laine W, Kouach M, Briand G, Vézin H, Gaslonde T et al. A transesterification reaction is implicated in the covalent binding of benzo[blacronycine anticancer agents with DNA and glutathione. Bioorg Med Chem 2004; 12: 23-9.
    • (2004) Bioorg Med Chem , vol.12 , pp. 23-29
    • David-Cordonnier, M.H.1    Laine, W.2    Kouach, M.3    Briand, G.4    Vézin, H.5    Gaslonde, T.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.