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E 3040
Known as:
E-3040
, E3040
National Institutes of Health
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Related topics
Related topics
3 relations
Broader (2)
Benzothiazoles
Pyridines
Narrower (1)
E3040 sulfate
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2009
2009
Construction of Triple-Transfected Cells [Organic Anion-Transporting Polypeptide (OATP) 1B1/Multidrug Resistance-Associated Protein (MRP) 2/MRP3 and OATP1B1/MRP2/MRP4] for Analysis of the Sinusoidal…
Masakazu Hirouchi
,
H. Kusuhara
,
R. Onuki
,
B. Ogilvie
,
A. Parkinson
,
Y. Sugiyama
Drug Metabolism And Disposition
2009
Corpus ID: 11792623
Multidrug resistance-associated protein (MRP) 3/ABCC3 and MRP4/ABCC4 are ATP-binding cassette (ABC) transporters expressed in the…
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Highly Cited
2005
Highly Cited
2005
Role of Breast Cancer Resistance Protein (Bcrp1/Abcg2) in the Extrusion of Glucuronide and Sulfate Conjugates from Enterocytes to Intestinal Lumen
Y. Adachi
,
H. Suzuki
,
A. Schinkel
,
Y. Sugiyama
Molecular Pharmacology
2005
Corpus ID: 9591434
The purpose of this study is to examine the significance of efflux transporters in the small intestine to extrude glucuronide (G…
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2001
2001
In vitro effects of E3040, a dual inhibitor of 5-lipoxygenase and thromboxane A(2) synthetase, on eicosanoid production.
K. Oketani
,
N. Nagakura
,
K. Harada
,
T. Inoue
European Journal of Pharmacology
2001
Corpus ID: 46404775
2001
2001
Effect of E3040, an inhibitor of 5-lipoxygenase and thromboxane synthase, on rat bowel damage induced by lipopolysaccharide.
K. Oketani
,
T. Inoue
,
M. Murakami
European Journal of Pharmacology
2001
Corpus ID: 31564865
2000
2000
Hepatic disposition of the acyl glucuronide 1-O-gemfibrozil-beta-D-glucuronide: effects of clofibric acid, acetaminophen, and acetaminophen glucuronide.
L. Sabordo
,
B. Sallustio
,
A. Evans
,
R. Nation
Journal of Pharmacology and Experimental…
2000
Corpus ID: 6077542
Glucuronidation of carboxylic acid compounds results in the formation of electrophilic acyl glucuronides. Because of their…
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Highly Cited
1997
Highly Cited
1997
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…
K. Niinuma
,
O. Takenaka
,
+4 authors
Y. Sugiyama
Journal of Pharmacology and Experimental…
1997
Corpus ID: 32468151
UNLABELLED Eisai hyperbilirubinemic rat (EHBR) is a mutant strain with a hereditary defect in canalicular multispecific organic…
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1997
1997
Carrier-mediated active transport of the glucuronide and sulfate of 6-hydroxy-5,7-dimethyl-2-methylamino-4-(3-pyridylmethyl) benzothiazole (E3040) into rat liver: quantitative comparison of…
O. Takenaka
,
T. Horie
,
H. Suzuki
,
Y. Sugiyama
Journal of Pharmacology and Experimental…
1997
Corpus ID: 30204110
The hepatic uptake of glucuronic acid and sulfate conjugates of 6-hydroxy-5,7-dimethyl-2-methylamino-4-(3-pyridylmethyl…
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Highly Cited
1995
Highly Cited
1995
Different biliary excretion systems for glucuronide and sulfate of a model compound; study using Eisai hyperbilirubinemic rats.
Osamu Takenaka
,
T. Horie
,
Hiroshi Suzuki
,
Yuichi Sugiyama
Journal of Pharmacology and Experimental…
1995
Corpus ID: 1450741
The disposition of conjugated metabolites (sulfate and glucuronide) was investigated in Eisai hyperbilirubinemic rats (EHBR) and…
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1995
1995
Kinetic Analysis of Hepatobiliary Transport for Conjugated Metabolites in the Perfused Liver of Mutant Rats (EHBR) with Hereditary Conjugated Hyperbilirubinemia
O. Takenaka
,
T. Horie
,
Kazuo Kobayashi
,
H. Suzuki
,
Y. Sugiyama
Pharmaceutical Research
1995
Corpus ID: 22995718
AbstractPurpose. Previously, we found that the biliary excretion of the 6-hydroxy-5,7-dimethyl-2-methylamino-4-(3-pyridylmethyl…
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1994
1994
Novel dual inhibitors of 5-lipoxygenase and thromboxane A2 synthetase: synthesis and structure-activity relationships of 3-pyridylmethyl-substituted 2-amino-6-hydroxybenzothiazole derivatives.
S. Hibi
,
Y. Okamoto
,
+7 authors
T. Inoue
Journal of Medicinal Chemistry
1994
Corpus ID: 25336476
As part of our search for novel antiinflammatory drug candidates, we have designed and synthesized a series of 3-pyridylmethyl…
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