메뉴 건너뛰기




Volumn 25, Issue 8, 1997, Pages 940-952

Orally active inhibitors of human leukocyte elastase. III. Identification and characterization of metabolites of L-694,458 by liquid chromatography-tandem mass spectrometry

Author keywords

[No Author keywords available]

Indexed keywords

DRUG METABOLITE; ENZYME INHIBITOR; LEUKOCYTE ELASTASE; N [(1,3 BENZODIOXOL 5 YL)BUTYL] 3,3 DIETHYL[4 [(4 METHYL 1 PIPERAZINYL)CARBONYL]PHENOXY] 4 OXO 1 AZETIDINECARBOXAMIDE; N [1 (1,3 BENZODIOXOL 5 YL)BUTYL] 3,3 DIETHYL 2 [4 [(4 METHYL 1 PIPERAZINYL)CARBONYL]PHENOXY] 4 OXO 1 AZETIDINECARBOXAMIDE; UNCLASSIFIED DRUG;

EID: 0030745408     PISSN: 00909556     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (16)

References (30)
  • 1
    • 0023220439 scopus 로고
    • Protease-antiprotease imbalance in the pathogenesis of emphysema and chronic bronchial injury: A potential target for drug development
    • G. L. Snider: Protease-antiprotease imbalance in the pathogenesis of emphysema and chronic bronchial injury: a potential target for drug development. Drug Dev. Res. 10, 235-253 (1987).
    • (1987) Drug Dev. Res. , vol.10 , pp. 235-253
    • Snider, G.L.1
  • 2
    • 0021318932 scopus 로고
    • Sputum soluble phase proteins and elastase activity in patients with cystic fibrosis
    • A. H. Jackson, S. L. Hill, S. C. Afford, and R. A. Stockley: Sputum soluble phase proteins and elastase activity in patients with cystic fibrosis. J. Respir. Dis. 65, 114-124 (1984).
    • (1984) J. Respir. Dis. , vol.65 , pp. 114-124
    • Jackson, A.H.1    Hill, S.L.2    Afford, S.C.3    Stockley, R.A.4
  • 3
    • 0023595113 scopus 로고
    • Synthetic inhibitors of human neutrophil elastase
    • D. A. Trainor: Synthetic inhibitors of human neutrophil elastase. Trends Pharmacol. Sci. 8, 303-307 (1987).
    • (1987) Trends Pharmacol. Sci. , vol.8 , pp. 303-307
    • Trainor, D.A.1
  • 7
    • 0026668818 scopus 로고
    • Inhibition of human serine proteases by substituted 2-azetidinones
    • W. B. Knight, R. Chabin, and B. Green: Inhibition of human serine proteases by substituted 2-azetidinones. Arch. Biochem. Biophys. 296, 704-708 (1992).
    • (1992) Arch. Biochem. Biophys. , vol.296 , pp. 704-708
    • Knight, W.B.1    Chabin, R.2    Green, B.3
  • 14
    • 0029839451 scopus 로고    scopus 로고
    • An asymmetric synthesis of L-694,458, a human leukocyte elastase inhibitor, via novel enzyme resolution of β-lactam esters
    • R. J. Cvetovich, M. Chartrain, F. W. Hartner, Jr., C. Roberge, J. S. Amato, and E. J. J. Grabowski: An asymmetric synthesis of L-694,458, a human leukocyte elastase inhibitor, via novel enzyme resolution of β-lactam esters. J. Org. Chem. 61, 6575-6580 (1996).
    • (1996) J. Org. Chem. , vol.61 , pp. 6575-6580
    • Cvetovich, R.J.1    Chartrain, M.2    Hartner Jr., F.W.3    Roberge, C.4    Amato, J.S.5    Grabowski, E.J.J.6
  • 15
    • 0025944905 scopus 로고
    • Biotransformation of lovastatin. IV. Identification of cytochrome P450 3A as the major enzyme responsible for the oxidative metabolism of lovastatin in rat and human liver microsomes
    • R. W. Wang, P. H. Kari, A. Y. H. Lu, P. E. Thomas, F. P. Guengerich, and K. P. Vyas: Biotransformation of lovastatin. IV. Identification of cytochrome P450 3A as the major enzyme responsible for the oxidative metabolism of lovastatin in rat and human liver microsomes. Arch. Biochem. Biophys. 290, 355-361 (1991).
    • (1991) Arch. Biochem. Biophys. , vol.290 , pp. 355-361
    • Wang, R.W.1    Kari, P.H.2    Lu, A.Y.H.3    Thomas, P.E.4    Guengerich, F.P.5    Vyas, K.P.6
  • 16
    • 0017101039 scopus 로고
    • Preparation of isolated rat liver cells
    • D.M. Prescot, ed., Academic Press, New York
    • P. O. Seglen: Preparation of isolated rat liver cells. In "Methods in Cell Biology," vol. 19 (D.M. Prescot, ed.), pp. 29-83. Academic Press, New York, 1976.
    • (1976) Methods in Cell Biology , vol.19 , pp. 29-83
    • Seglen, P.O.1
  • 17
    • 0024308532 scopus 로고
    • Methyltransferase pharmacogenetics
    • R. Weinshilboum: Methyltransferase pharmacogenetics. Pharmacol. Ther. 43, 77-90 (1989).
    • (1989) Pharmacol. Ther. , vol.43 , pp. 77-90
    • Weinshilboum, R.1
  • 18
    • 0015508735 scopus 로고
    • Accumulation and elimination of a novel metabolite during chronic administration of the phenothiazine drug perazine to rats
    • U. Breyer: Accumulation and elimination of a novel metabolite during chronic administration of the phenothiazine drug perazine to rats. Biochem. Pharmacol. 21, 1419-1429 (1972).
    • (1972) Biochem. Pharmacol. , vol.21 , pp. 1419-1429
    • Breyer, U.1
  • 19
    • 0016301083 scopus 로고
    • Tissue metabolites of trifluoperazine, fluphenazine, prochlorperazine and perphenazine in the rat: Identification and synthesis
    • U. Breyer, A. Prox, R. Bertele, and H. J. Gaertner: Tissue metabolites of trifluoperazine, fluphenazine, prochlorperazine and perphenazine in the rat: identification and synthesis. J. Pharm. Sci. 63, 1842-1848 (1974).
    • (1974) J. Pharm. Sci. , vol.63 , pp. 1842-1848
    • Breyer, U.1    Prox, A.2    Bertele, R.3    Gaertner, H.J.4
  • 20
    • 0015355592 scopus 로고
    • In vivo piperazine ring degradation in neuroleptic and antihistaminic drugs
    • H. J. Gaertner and U. Breyer: In vivo piperazine ring degradation in neuroleptic and antihistaminic drugs. Arzneim.-Forsch. (Drug Res.) 22, 1084-1085 (1972).
    • (1972) Arzneim.-Forsch. (Drug Res.) , vol.22 , pp. 1084-1085
    • Gaertner, H.J.1    Breyer, U.2
  • 21
    • 0015719725 scopus 로고
    • Chronic administration of chlorcyclizine and meclizine to rats: Accumulation of a metabolite formed by piperazine ring cleavage
    • H. J. Gaertner, U. Breyer, and G. Liomin: Chronic administration of chlorcyclizine and meclizine to rats: Accumulation of a metabolite formed by piperazine ring cleavage. J. Pharmacol. Exp. Ther. 185, 195-201 (1973).
    • (1973) J. Pharmacol. Exp. Ther. , vol.185 , pp. 195-201
    • Gaertner, H.J.1    Breyer, U.2    Liomin, G.3
  • 22
    • 0023792429 scopus 로고
    • Metabolism of a new positive inotropic agent, 3,4-dihydro-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-2(1H)-quinolinone (OPC-8212) in the rat, mouse, dog, monkey and human
    • G. Miyamoto, H. Sasabe, N. Tominaga, N. Uegaki, M. Tominaga, and T. Shimizu: Metabolism of a new positive inotropic agent, 3,4-dihydro-6-[4-(3,4-dimethoxybenzoyl)-1-piperazinyl]-2(1H)-quinolinone (OPC-8212) in the rat, mouse, dog, monkey and human. Xenobiotica 18, 1143-1155 (1988).
    • (1988) Xenobiotica , vol.18 , pp. 1143-1155
    • Miyamoto, G.1    Sasabe, H.2    Tominaga, N.3    Uegaki, N.4    Tominaga, M.5    Shimizu, T.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.