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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

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4 relations

Broader (4)

Affinity LabelsAzidesDihydropyridinesdihydropyridine

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2004
2004
Substitution of threonine-1351 in the multidrug transporter Cdr1p of Candida albicans results in hypersusceptibility to antifungal agents and threonine-1351 is essential for synergic effects of…
OBJECTIVES Functional characterization of a mutant Candida albicans drug resistance protein (Cdr1p) by overexpression in… 
2001
2001
Impact of the basic amine on the biological activity and intracellular distribution of an aza-anthrapyrazole: BBR 3422.
Highly Cited
1996
Highly Cited
1996
Synthetic hydrophobic peptides are substrates for P-glycoprotein and stimulate drug transport.
P-Glycoprotein functions as an ATP-driven active efflux pump for many natural products and chemotherapeutic drugs. Hydrophobic… 
1996
1996
On the mechanism of action of doxorubicin encapsulation in nanospheres for the reversal of multidrug resistance
Abstract We had previously shown that doxorubicin encapsulation in polyisohexylcyanocrylate nanospheres could circumvent the P… 
1996
1996
Reversal of multi‐drug resistance in vitro by fatty acid PEG fatty acid diesters
Fatty acid ester surfactants, e.g., Cremophor EL and Solutol HS 15, that modulate multi‐drug resistance (MDR) have been described… 
Highly Cited
1995
Highly Cited
1995
Effects of lipids on ATPase activity of purified Chinese hamster P-glycoprotein.
Chinese hamster P-glycoprotein ("multidrug-resistance protein") was purified and reconstituted in proteoliposomes by the… 
1993
1993
Expression of the multidrug transporter, P‐glycoprotein, in renal and transitional cell carcinomas
Background. Renal cell carcinomas (RCC) respond poorly to anthracyclines, Vinca alkaloids, and other agents. P‐glycoprotein is… 
1993
1993
Multidrug‐resistant human kb carcinoma cells are highly resistant to the protein phosphatase inhibitors okadaic acid and calyculin A. Analysis of potential mechanisms involved in toxin resistance
In this study we show that multidrug‐resistant (MDR) human KB‐VI cells are highly resistant to the cytotoxicity of okadaic acid… 
1993
1993
Effect of Staurosporine Derivatives on Protein Kinase Activity and Vinblastine Accumulation in Mouse Leukaemia P388/ADR Cells
Abstract— Inhibition by staurosporine derivatives of cyclic AMP‐dependent protein kinase (A‐kinase) and protein kinase C (C… 
Highly Cited
1991
Highly Cited
1991
Agents which reverse multidrug-resistance are inhibitors of [3H]vinblastine transport by isolated vesicles.
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