849668-91-3 Usage
Description
BenzaMide, 2-aMino-N-[4-[2-(3,4-dihydro-6,7-diMethoxy-2(1H)-isoquinolinyl)ethyl]phenyl]-4,5-diMethoxyis a complex organic compound that serves as an intermediate in the synthesis of Tariquidar (T007600), a P-glycoprotein drug efflux pump inhibitor. BenzaMide, 2-aMino-N-[4-[2-(3,4-dihydro-6,7-diMethoxy-2(1H)-isoquinolinyl)ethyl]phenyl]-4,5-diMethoxyis characterized by its unique molecular structure, which includes a benzamide core with various substituents, such as amino, isoquinolinyl, and dimethoxy groups. Its role in the synthesis of Tariquidar highlights its potential applications in the pharmaceutical industry, particularly in the development of cancer treatments.
Uses
Used in Pharmaceutical Industry:
BenzaMide, 2-aMino-N-[4-[2-(3,4-dihydro-6,7-diMethoxy-2(1H)-isoquinolinyl)ethyl]phenyl]-4,5-diMethoxyis used as an intermediate in the synthesis of Tariquidar (T007600) for its potential application in cancer treatment. Tariquidar is a P-glycoprotein drug efflux pump inhibitor, which can help overcome multidrug resistance in cancer cells by inhibiting the efflux of chemotherapeutic agents, thereby increasing their intracellular concentration and effectiveness. This makes BenzaMide a valuable component in the development of novel cancer therapies and improving the efficacy of existing treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 849668-91-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,6,6 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 849668-91:
(8*8)+(7*4)+(6*9)+(5*6)+(4*6)+(3*8)+(2*9)+(1*1)=243
243 % 10 = 3
So 849668-91-3 is a valid CAS Registry Number.
849668-91-3Relevant articles and documents
DEUTERATED ANALOGS OF TARIQUIDAR
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Paragraph 0314-0315, (2019/11/22)
The present invention relates to efflux inhibitor compounds, compositions, and methods of using the same. More specifically, the instant invention comprises deuterated analogs of tariquidar with superior pharmacokinetic properties such that it is now poss
NOVEL P-GLYCOPROTEIN INHIBITOR, METHOD FOR THE PREPARATION THEREOF AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME
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Page/Page column 14-15, (2008/06/13)
A p-glycoprotein inhibitor of Formula 1 is capable of effectively preventing the development of multi-drug resistance directed to an anticancer agent in cancer cells, and greatly enhances the bioavailability of the drug, such as paclitaxel, which is not readily absorbed when orally administered.