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Volumn 21, Issue 4, 2003, Pages 413-420

Quinolizidinyl derivatives of iminodibenzyl and phenothiazine as multidrug resistance modulators in ovarian cancer cells

Author keywords

Chemosensitizers; Cytotoxicity; Iminodibenzyl derivatives; Ovarian cancer cells; Phenothiazine derivatives; Quinolizidinyl derivatives

Indexed keywords

BENZENE DERIVATIVE; BENZYL DERIVATIVE; CLOMIPRAMINE; DOXORUBICIN; GLYCOPROTEIN P; ISOPROTEIN; PHENOTHIAZINE DERIVATIVE; QUINOLIZIDINE DERIVATIVE;

EID: 1642452917     PISSN: 01676997     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1026295017158     Document Type: Article
Times cited : (18)

References (26)
  • 1
    • 0025007511 scopus 로고
    • Pharmacology of drugs that alter multidrug resistance in cancer
    • Ford JM, Hait WN: Pharmacology of drugs that alter multidrug resistance in cancer. Pharmacol Rev 42: 155-199, 1990
    • (1990) Pharmacol Rev , vol.42 , pp. 155-199
    • Ford, J.M.1    Hait, W.N.2
  • 2
    • 0030738677 scopus 로고    scopus 로고
    • Multidrug resistance: Molecular mechanisms and clinical relevance
    • Ling V: Multidrug resistance: molecular mechanisms and clinical relevance. Cancer Chemother Pharmacol 40(suppl.): S3-S8, 1997
    • (1997) Cancer Chemother Pharmacol , vol.40 , Issue.SUPPL.
    • Ling, V.1
  • 4
    • 0036405919 scopus 로고    scopus 로고
    • Overcoming multidrug resistance in taxane chemotherapy
    • Geney R, Ungureanu M, Li D, Ojima I: Overcoming multidrug resistance in taxane chemotherapy. Clin Chem Lab Med 40: 918-925, 2002
    • (2002) Clin Chem Lab Med , vol.40 , pp. 918-925
    • Geney, R.1    Ungureanu, M.2    Li, D.3    Ojima, I.4
  • 5
    • 0035047222 scopus 로고    scopus 로고
    • Structure-activity relationship of multidrug resistance reversers
    • Wiese M, Pajeva IK: Structure-activity relationship of multidrug resistance reversers. Curr Med Chem 8: 685-713, 2001
    • (2001) Curr Med Chem , vol.8 , pp. 685-713
    • Wiese, M.1    Pajeva, I.K.2
  • 6
    • 0037052062 scopus 로고    scopus 로고
    • The medicinal chemistry of multidrug resistance (MDR) reversing drugs
    • Teodori E, Dei S, Scapecchi S, Gualtieri F: The medicinal chemistry of multidrug resistance (MDR) reversing drugs. Farmaco 57: 385-415, 2002
    • (2002) Farmaco , vol.57 , pp. 385-415
    • Teodori, E.1    Dei, S.2    Scapecchi, S.3    Gualtieri, F.4
  • 7
    • 0024534226 scopus 로고
    • Structural features determining activity of phenothiazines and related drugs for inhibition of cell growth and reversal of multidrug resistance
    • Ford MJ, Prozialeck WC, Hait WN: Structural features determining activity of phenothiazines and related drugs for inhibition of cell growth and reversal of multidrug resistance. Mol Pharmacol 35: 105-115, 1989
    • (1989) Mol Pharmacol , vol.35 , pp. 105-115
    • Ford, M.J.1    Prozialeck, W.C.2    Hait, W.N.3
  • 8
    • 0025267821 scopus 로고
    • Cellular and biochemical characterization of thioxanthenes for reversal of multidrug resistance in human and murine cell lines
    • Ford JM, Bruggeman EP, Pastan I, Gottesman MM, Hait WN: Cellular and biochemical characterization of thioxanthenes for reversal of multidrug resistance in human and murine cell lines. Cancer Res 50: 1748-1756, 1990
    • (1990) Cancer Res , vol.50 , pp. 1748-1756
    • Ford, J.M.1    Bruggeman, E.P.2    Pastan, I.3    Gottesman, M.M.4    Hait, W.N.5
  • 9
    • 0026624915 scopus 로고
    • Reversal of multidrug resistance by phenothiazines and structurally related compounds
    • Ramu A, Ramu N: Reversal of multidrug resistance by phenothiazines and structurally related compounds. Cancer Chemother Pharmacol 30: 165-173, 1992
    • (1992) Cancer Chemother Pharmacol , vol.30 , pp. 165-173
    • Ramu, A.1    Ramu, N.2
  • 10
    • 0030898431 scopus 로고    scopus 로고
    • QSAR and molecular modelling of catamphiphilic drugs able to modulate multidrug resistance in tumors
    • Pajeva IK, Wiese M: QSAR and molecular modelling of catamphiphilic drugs able to modulate multidrug resistance in tumors. Quant Struct Act Relat 16: 1-10, 1997
    • (1997) Quant Struct Act Relat , vol.16 , pp. 1-10
    • Pajeva, I.K.1    Wiese, M.2
  • 11
    • 0032554868 scopus 로고    scopus 로고
    • Molecular modeling of phenothiazines and related drugs as multidrug resistance modifier: A comparative molecular field analysis study
    • Pajeva IK, Wiese M: Molecular modeling of phenothiazines and related drugs as multidrug resistance modifier: a comparative molecular field analysis study. J Med Chem 41: 1815-1826, 1998
    • (1998) J Med Chem , vol.41 , pp. 1815-1826
    • Pajeva, I.K.1    Wiese, M.2
  • 12
    • 1642551344 scopus 로고
    • Derivati di amminoalcoli e diammine naturali di interesse farmacologico. Nota III. Sintesi di derivati lupinilici di sistemi eterociclici trianellari
    • Sparatore F, Boido V: Derivati di amminoalcoli e diammine naturali di interesse farmacologico. Nota III. Sintesi di derivati lupinilici di sistemi eterociclici trianellari. Ann Chim 54: 591-601, 1964
    • (1964) Ann Chim , vol.54 , pp. 591-601
    • Sparatore, F.1    Boido, V.2
  • 13
    • 0020057908 scopus 로고
    • Chinolizidinil derivati di sistemi triciclici
    • Boido V, Sparatore A: Chinolizidinil derivati di sistemi triciclici. Farmaco 37: 63-73, 1982
    • (1982) Farmaco , vol.37 , pp. 63-73
    • Boido, V.1    Sparatore, A.2
  • 14
    • 0028350706 scopus 로고
    • Preparation and pharmacological activities of 10-homolupinanoyl-2-R- phenothiazines
    • Sparatore A, Sparatore F: Preparation and pharmacological activities of 10-homolupinanoyl-2-R-phenothiazines. Farmaco 49: 5-17, 1994
    • (1994) Farmaco , vol.49 , pp. 5-17
    • Sparatore, A.1    Sparatore, F.2
  • 15
    • 0033581641 scopus 로고    scopus 로고
    • Quinolizidinyl derivatives of 511-dihydro-6H-pyrido2,3-b-1,4 benzodiazepin-6-one as ligands for muscarinic receptors
    • Novelli F, Sparatore A, Tasso B, Sparatore F: Quinolizidinyl derivatives of 511-dihydro-6H-pyrido(2,3-b(-(1,4( benzodiazepin-6-one as ligands for muscarinic receptors. Bioorg Med Chem Lett 9: 3031-3034, 1999
    • (1999) Bioorg Med Chem Lett , vol.9 , pp. 3031-3034
    • Novelli, F.1    Sparatore, A.2    Tasso, B.3    Sparatore, F.4
  • 17
    • 0027179609 scopus 로고
    • Cytoplasmic membrane cholesterol and doxorubicin cytotoxicity in drug-sensitive and multidrug-resistant human ovarian cancer cells
    • Mazzoni A, Trave F: Cytoplasmic membrane cholesterol and doxorubicin cytotoxicity in drug-sensitive and multidrug-resistant human ovarian cancer cells. Oncol Res 5: 75-82, 1993
    • (1993) Oncol Res , vol.5 , pp. 75-82
    • Mazzoni, A.1    Trave, F.2
  • 18
    • 26744444772 scopus 로고
    • N-Acyl derivatives of iminodibenzyl
    • US2, 666,051
    • Häfliger F, Schindler W: N-Acyl derivatives of iminodibenzyl. US2, 666,051. Chem Abstr 49: 9041f, 1955
    • (1955) Chem Abstr , vol.49
    • Häfliger, F.1    Schindler, W.2
  • 19
    • 0141805132 scopus 로고
    • Phenothiazine derivatives of pharmacological interest
    • Ekstrand T: Phenothiazine derivatives of pharmacological interest. Acta Chem Scand 3: 302-303, 1949
    • (1949) Acta Chem Scand , vol.3 , pp. 302-303
    • Ekstrand, T.1
  • 20
    • 84986441082 scopus 로고
    • Phenothiazine derivatives
    • Brit 740, 932
    • Société des usines chimiques Rhone-Poulenc. Phenothiazine derivatives. Brit 740, 932. Chem Abstr 51: 500i, 1957
    • (1957) Chem Abstr , vol.51
  • 22
    • 0141693575 scopus 로고
    • Phenothiazine derivatives. VI. Experiments for the preparation of phenothiazines with selective coronary dilator activity
    • Toldy L, Toth I, Fekete M, Borsy J: Phenothiazine derivatives. VI. Experiments for the preparation of phenothiazines with selective coronary dilator activity. Acta Chim Acad Sci Hung 44: 301-325, 1965
    • (1965) Acta Chim Acad Sci Hung , vol.44 , pp. 301-325
    • Toldy, L.1    Toth, I.2    Fekete, M.3    Borsy, J.4
  • 23
    • 0027250018 scopus 로고
    • Thiolupinine and some derivatives of pharmacological interest
    • Novelli F, Sparatore F: Thiolupinine and some derivatives of pharmacological interest. Farmaco 48: 1021-1049, 1993
    • (1993) Farmaco , vol.48 , pp. 1021-1049
    • Novelli, F.1    Sparatore, F.2
  • 24
    • 0345410533 scopus 로고
    • Pharmacologie des Tofranil (N-(3-dymethylaminopropyl)-iminodibenzyl hydrochloride)
    • Domenjoz R, Theobald W: Pharmacologie des Tofranil (N-(3- dymethylaminopropyl)-iminodibenzyl hydrochloride). Arch Int Pharmacodyn 120: 450-489, 1959
    • (1959) Arch Int Pharmacodyn , vol.120 , pp. 450-489
    • Domenjoz, R.1    Theobald, W.2
  • 25
    • 0019361067 scopus 로고
    • Pharmacological evaluation of 2-(4-methylaminobuthoxy)diphenylmethane hydrochloride, a new psychotropic drug with antidepressant activity
    • Tobe A, Yoshida Y, Ikoma H, Tonomura S, Kikumoto R: Pharmacological evaluation of 2-(4-methylaminobuthoxy)diphenylmethane hydrochloride, a new psychotropic drug with antidepressant activity. Arzneim Forsch 31: 1278-1285, 1981
    • (1981) Arzneim Forsch , vol.31 , pp. 1278-1285
    • Tobe, A.1    Yoshida, Y.2    Ikoma, H.3    Tonomura, S.4    Kikumoto, R.5
  • 26
    • 0037142379 scopus 로고    scopus 로고
    • Design, synthesis and evaluation of new chemosensitizers in multi-drug resistant Plasmodium falciparum
    • Guan J, Kyle DE, Gerena L, Zhang Q, Milhous WK, Lin AJ: Design, synthesis and evaluation of new chemosensitizers in multi-drug resistant Plasmodium falciparum. J Med Chem 45: 2741-2748, 2002
    • (2002) J Med Chem , vol.45 , pp. 2741-2748
    • Guan, J.1    Kyle, D.E.2    Gerena, L.3    Zhang, Q.4    Milhous, W.K.5    Lin, A.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.