azidopine

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

Topic mentions per year

Topic mentions per year

1987-2006
051019872006

Papers overview

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1996
1996
Using three different cell lines exhibiting the MDR phenotype, we have studied the ability of eight different modulators to… (More)
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1995
Highly Cited
1995
Identifying new chemotherapeutic agents and characterizing mechanisms of resistance may improve cancer treatment. The Anticancer… (More)
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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… (More)
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1992
1992
To determine the number of drug binding sites that exist on the multidrug transporter, P-glycoprotein, we used azidopine, a… (More)
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1991
1991
It is believed that P-glycoprotein (P-gp) is an energy-dependent drug efflux pump responsible for decreased drug accumulation in… (More)
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1991
1991
To identify the binding domain for dihydropyridine Ca2+ antagonists, skeletal muscle Ca2+ channels were photolabeled with [3H… (More)
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1991
1991
The dihydropyridine binding site of the rabbit skeletal muscle calcium channel alpha 1 subunit was identified using tritiated… (More)
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1990
1990
Verapamil has been proposed to modulate the multidrug resistance phenotype by competitive inhibition of an energy dependent… (More)
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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… (More)
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1987
1987
A radioactive photoactive dihydropyridine calcium channel blocker, [3H]azidopine, was used to photoaffinity label plasma… (More)
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