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azidopine

Known as: 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-4-(2-(trifluoromethyl)phenyl)-, 2-((4-azidobenzoyl)amino)ethyl ethyl ester 
 
National Institutes of Health

Papers overview

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Highly Cited
2003
Highly Cited
2003
The overexpression of P-glycoprotein (Pgp) or the multidrug resistance-associated protein (MRP) confers multidrug resistance (MDR… Expand
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Highly Cited
2003
Highly Cited
2003
In view of the importance of Candida drug resistance protein (Cdr1p) in azole resistance, we have characterized it by… Expand
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Highly Cited
1995
Highly Cited
1995
Identifying new chemotherapeutic agents and characterizing mechanisms of resistance may improve cancer treatment. The Anticancer… Expand
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Highly Cited
1992
Highly Cited
1992
We expressed human MDR1 cDNA isolated from the human adrenal gland in porcine LLC-PK1 cells. A highly polarized epithelium formed… Expand
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Highly Cited
1992
Highly Cited
1992
To determine the number of drug binding sites that exist on the multidrug transporter, P-glycoprotein, we used azidopine, a… Expand
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Highly Cited
1991
Highly Cited
1991
It is believed that P-glycoprotein (P-gp) is an energy-dependent drug efflux pump responsible for decreased drug accumulation in… Expand
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1991
1991
To identify the binding domain for dihydropyridine Ca2+ antagonists, skeletal muscle Ca2+ channels were photolabeled with [3H… Expand
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1991
1991
The dihydropyridine binding site of the rabbit skeletal muscle calcium channel alpha 1 subunit was identified using tritiated… Expand
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1989
1989
Cells that express P-glycoprotein are resistant to many unrelated anticancer drugs. All evidence suggests that P-glycoprotein is… Expand
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Highly Cited
1988
Highly Cited
1988
  • Ahmad R. Safa
  • Proceedings of the National Academy of Sciences…
  • 1988
  • Corpus ID: 46234938
Verapamil, a phenylalkylamine calcium channel blocker, has been shown to reverse multidrug resistance in tumor cells, possibly by… Expand
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