Product Name |
(S)-Cinacalcet-D3 |
Alternate Names |
Cinacalcet Stable Isotopes, Stable Isotopes of Cinacalcet |
CAT No. |
CS-O-38751
|
CAS No. |
694495-47-1 (unlabelled) |
Category |
Stable Isotopes |
Stock |
Enquire
|
Mol. Wt. |
360.43 g/mol |
Mol. For. |
C22H19D3F3N
|
Hazardous |
This is not a Hazardous Compound
|
COA |
View Sample COA
|
MSDS |
View Sample MSDS
|
Parent API |
Cinacalcet |
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 |
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(S)-Cinacalcet-D3 is a deuterated analog of the drug Cinacalcet, which is used for the treatment of hyperparathyroidism and hypercalcemia in patients with chronic kidney disease. The deuterated form of the drug, (S)-Cinacalcet-D3, is used in research and development to study the pharmacokinetics and metabolism of Cinacalcet.
The mechanism of action of Cinacalcet and its deuterated analog involves binding to the calcium-sensing receptor (CaSR) on the parathyroid gland, which suppresses the secretion of parathyroid hormone (PTH). This leads to a decrease in the levels of calcium in the blood, which is beneficial for patients with hyperparathyroidism and hypercalcemia.
The chemical formula of (S)-Cinacalcet-D3 is C22H22D3F3N, and it has a molecular weight of 351.42 g/mol. The drug is administered orally, with a recommended dosage of 30-180 mg per day. (S)-Cinacalcet-D3 is metabolized by the liver, primarily through the cytochrome P450 system. The drug has a half-life of approximately 30 hours and is excreted in the urine and feces.
(S)-Cinacalcet-D3 is an important tool in the study of the pharmacokinetics and metabolism of Cinacalcet. Its deuterated form allows for more accurate measurements of the drug's distribution, elimination, and bioavailability in the body.