Product Name |
Nicardipine-D3 |
Alternate Names |
Nicardipine Stable Isotopes, Stable Isotopes of Nicardipine |
CAT No. |
CS-O-41299
|
CAS No. |
Not Available |
Category |
Stable Isotopes |
Stock |
IN-Stock
|
Mol. Wt. |
482.22 g/mol |
Mol. For. |
C₂₆H₂₆D₃N₃O₆
|
Hazardous |
This is not a Hazardous Compound
|
COA |
View Sample COA
|
MSDS |
View Sample MSDS
|
Parent API |
Nicardipine |
Controlled |
No |
Shipping |
Free for purchase above 1000$ |
Delivery |
In-Stock, products will be dispatched within 24 hours via FedEx for USA, Europe, and other countries. |
Return |
Returns/replacement accepted if you are not satisfied with the quality of the product, (please send us an email with the reason/issues which are facing, within 15 days, after receipt of the product). |
Ordering |
Place your order online or by email sales@clearsynth.com |
If you find a better price anywhere else we guarantee Price match.
Nicardipine-D3 is a deuterated version of the calcium channel blocker Nicardipine. It is commonly used in the treatment of high blood pressure, angina, and other cardiovascular conditions. Nicardipine-D3 is a selective dihydropyridine calcium channel blocker that works by inhibiting the influx of calcium ions into vascular smooth muscle cells and cardiac myocytes.
The deuterium substitution in Nicardipine-D3 provides a useful tool for pharmacokinetic and pharmacodynamic studies. Deuterium is a stable isotope of hydrogen that has a slightly higher mass, which can result in slower metabolism and elimination of the drug from the body. This can lead to longer-lasting and more consistent drug effects, making Nicardipine-D3 a valuable tool in clinical research.
In terms of chemical information, Nicardipine-D3 has a molecular formula of C26H27D3N2O6 and a molecular weight of 471.57 g/mol. It has a half-life of approximately 8 hours and is primarily metabolized in the liver. Nicardipine-D3 is available in both oral and intravenous formulations and is typically administered under medical supervision.
Overall, Nicardipine-D3 is a valuable drug for the treatment of cardiovascular conditions and for use in clinical research. Its deuterium substitution provides a useful tool for pharmacokinetic and pharmacodynamic studies, and its selective calcium channel blocking properties make it a highly effective treatment option.