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Journal Abstract Search

276 related items for PubMed ID: 9067317

  • 1. Temocaprilat, a novel angiotensin-converting enzyme inhibitor, is excreted in bile via an ATP-dependent active transporter (cMOAT) that is deficient in Eisai hyperbilirubinemic mutant rats (EHBR).
    Ishizuka H, Konno K, Naganuma H, Sasahara K, Kawahara Y, Niinuma K, Suzuki H, Sugiyama Y.
    J Pharmacol Exp Ther; 1997 Mar; 280(3):1304-11. PubMed ID: 9067317
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  • 2. Trandolaprilat, an angiotensin-converting enzyme inhibitor, is not excreted in bile via an ATP-dependent active transporter (cMOAT).
    Shionoiri H, Takasaki I, Minamisawa K, Ishizuka H, Konno K, Naganuma H, Sasahara K, Kawahara Y.
    Hypertens Res; 2001 May; 24(3):235-40. PubMed ID: 11409646
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  • 3. Carrier-mediated mechanism for the biliary excretion of the quinolone antibiotic grepafloxacin and its glucuronide in rats.
    Sasabe H, Tsuji A, Sugiyama Y.
    J Pharmacol Exp Ther; 1998 Mar; 284(3):1033-9. PubMed ID: 9495864
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  • 4. Species differences in the transport activity for organic anions across the bile canalicular membrane.
    Ishizuka H, Konno K, Shiina T, Naganuma H, Nishimura K, Ito K, Suzuki H, Sugiyama Y.
    J Pharmacol Exp Ther; 1999 Sep; 290(3):1324-30. PubMed ID: 10454510
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  • 5. Methotrexate is excreted into the bile by canalicular multispecific organic anion transporter in rats.
    Masuda M, I'izuka Y, Yamazaki M, Nishigaki R, Kato Y, Ni'inuma K, Suzuki H, Sugiyama Y.
    Cancer Res; 1997 Aug 15; 57(16):3506-10. PubMed ID: 9270020
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  • 6. Biliary excretion of pravastatin in rats: contribution of the excretion pathway mediated by canalicular multispecific organic anion transporter.
    Yamazaki M, Akiyama S, Ni'inuma K, Nishigaki R, Sugiyama Y.
    Drug Metab Dispos; 1997 Oct 15; 25(10):1123-9. PubMed ID: 9321514
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  • 7. Kinetic analysis of the primary active transport of conjugated metabolites across the bile canalicular membrane: comparative study of S-(2,4-dinitrophenyl)-glutathione and 6-hydroxy-5,7-dimethyl-2-methylamino-4-(3-pyridylmethyl)benzothiazole glucuronide.
    Niinuma K, Takenaka O, Horie T, Kobayashi K, Kato Y, Suzuki H, Sugiyama Y.
    J Pharmacol Exp Ther; 1997 Aug 15; 282(2):866-72. PubMed ID: 9262353
    [Abstract] [Full Text] [Related]

  • 8. Carrier-mediated hepatobiliary transport of a novel antifolate, N-[4-[(2,4-dianninopteridine-6-yl)methyl]-3,4-dihydro-2H-1,4-benzothiazin-7-yl]carbonyl-L-homoglutamic acid, in rats.
    Han YH, Kato Y, Watanabe Y, Terao K, Asoh Y, Sugiyama Y.
    Drug Metab Dispos; 2001 Apr 15; 29(4 Pt 1):394-400. PubMed ID: 11259322
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  • 14. Reduced folate derivatives are endogenous substrates for cMOAT in rats.
    Kusuhara H, Han YH, Shimoda M, Kokue E, Suzuki H, Sugiyama Y.
    Am J Physiol; 1998 Oct 15; 275(4):G789-96. PubMed ID: 9756510
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  • 16. Primary active transport of pravastatin across the liver canalicular membrane in normal and mutant Eisai hyperbilirubinaemic rats.
    Yamazaki M, Kobayashi K, Sugiyama Y.
    Biopharm Drug Dispos; 1996 Nov 15; 17(8):645-59. PubMed ID: 8950045
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  • 18. Primary active transport of peptidic endothelin antagonists by rat hepatic canalicular membrane.
    Akhteruzzaman S, Kato Y, Hisaka A, Sugiyama Y.
    J Pharmacol Exp Ther; 1999 Feb 15; 288(2):575-81. PubMed ID: 9918561
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  • 20. Stereoselective hepatobiliary transport of the quinolone antibiotic grepafloxacin and its glucuronide in the rat.
    Sasabe H, Kato Y, Tsuji A, Sugiyama Y.
    J Pharmacol Exp Ther; 1998 Feb 15; 284(2):661-8. PubMed ID: 9454812
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