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Tariquidar-d4

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Product Code: CS-T-102052 Stable Isotopes Research Use Only
Tariquidar-d4
Category
Stable Isotopes
API Family
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Product Code
CS-T-102052
Research Status
For Laboratory Use

Tariquidar-d4

Stable Isotopes
Stock Status: : Enquire Live

CAT No.
CS-T-102052
CAS No.
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Molecular Formula
C38H34D4N4O6
Molecular Weight
650.76
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There is no hazardous surcharge associated with this product.
There is no packaging charge associated with this product.
For Research Purposes only. Not for Personal or Veterinary use.
All compounds supplied are strictly intended for laboratory, research, analytical, and scientific use only. They are not meant for human consumption, therapeutic use, or any form of clinical application.
CAS No.
-
Product Code
CS-T-102052
M.F.
C38H34D4N4O6
M.W.
650.76
Category
Stable Isotopes
Storage Condition
Refer MSDS for complete information.
IUPAC Name
Tariquidar-d4
References
"Fox, E., et al.: Expert. Rev. Ainticancer. Ther., 7, 447 (2007); Hernandez, D., et al.: Biochem. Pharmacol., 85, 21 (2013); Bauer, F., et al.: Euro. J. Pharmacol., 696, 18 (2012);"
Synonyms
"N-[2-[[[4-[2-(3,4-Dihydro-6,7-dimethoxy-2(1H)-isoquinolinyl)ethyl]phenyl]amino]carbonyl]-4,5-dimethoxyphenyl]-3-quinolinecarboxamide-d4; XR 9576-d4;"
Application Notes
"Isotope Labelled analogue of Tariquidar (T007600), a p-glycoprotein drug efflux pump inhibitor. Tariquidar inhibits the ATPase activity of P-glycoprotein, suggesting that the modulating effect is derived from the inhibition of substrate binding, inhibition of ATP hydrolysis or both.Tariquidar can be considered an ideal agent for testing the role of P-glycoprotein inhibition in cancer"
Hazard Compound
Refer MSDS for complete information.
Overview
"Isotope Labelled analogue of Tariquidar (T007600), a p-glycoprotein drug efflux pump inhibitor. Tariquidar inhibits the ATPase activity of P-glycoprotein, suggesting that the modulating effect is derived from the inhibition of substrate binding, inhibition of ATP hydrolysis or both.Tariquidar can be considered an ideal agent for testing the role of P-glycoprotein inhibition in cancer"

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