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Volumn 21, Issue 2 A, 2001, Pages 847-856

Influence of beta-adrenergic antagonists, H1-receptor blockers, analgesics, diuretics, and quinolone antibiotics on the cellular accumulation of the anticancer drug, daunorubicin: P-glycoprotein modulation

Author keywords

Daunorubicin; Drug classes; Multidrug resistance; P glycoprotein

Indexed keywords

ACEBUTOLOL; ANALGESIC AGENT; ANTINEOPLASTIC AGENT; ASTEMIZOLE; ATENOLOL; BETA ADRENERGIC RECEPTOR BLOCKING AGENT; CLEMASTINE; DAUNORUBICIN; DEXTROPROPOXYPHENE; DIPHENHYDRAMINE; DIURETIC AGENT; GLYCOPROTEIN P; HISTAMINE H1 RECEPTOR ANTAGONIST; HYDROXYZINE; KETOCONAZOLE; LABETALOL; LOPERAMIDE; METOPROLOL; MULTIDRUG RESISTANCE PROTEIN; NADOLOL; PETHIDINE; PINDOLOL; PIROXICAM; PROPRANOLOL; QUINOLONE DERIVATIVE; RHODAMINE 123; TERFENADINE; TRIPROLIDINE; UNINDEXED DRUG;

EID: 0035021840     PISSN: 02507005     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (18)

References (48)
  • 4
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    • Expression and function of P-glycoprotein (MDR1 gene product) in normal and malignant tissues
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    • Sugawara, I.1
  • 8
    • 0029983195 scopus 로고    scopus 로고
    • High level expression of the multidrug resistance (MDR1) gene in normal bladder urothelium: A potential involvement in protection against carcinogens
    • (1996) Carcinogenesis , vol.17 , pp. 601-604
    • Clifford, S.C.1    Neal, D.E.2    Lunec, J.3
  • 9
    • 0033328139 scopus 로고    scopus 로고
    • The contribution of P-glycoprotein to pharmacokinetic drug-drug interactions
    • (1999) J Clin Pharmacol , vol.39 , pp. 1203-0121
    • Yu, D.K.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.