Product Name |
Sorafenib D3 |
Alternate Names |
Sorafenib Stable Isotopes, Stable Isotopes of Sorafenib |
CAT No. |
CS-O-10301
|
CAS No. |
1130115-44-4 |
Category |
Stable Isotopes |
Stock |
IN-Stock
|
Mol. Wt. |
467.84 g/mol |
Mol. For. |
C21H13D3ClF3N4O3
|
Hazardous |
This is not a Hazardous Compound
|
COA |
View Sample COA
|
MSDS |
View Sample MSDS
|
Parent API |
Sorafenib |
Purity |
Not less than 90 % |
Therapeutic |
Anti-Cancer / Oncology |
Smileys |
O=C(NC([2H])([2H])[2H])C1=CC(OC2=CC=C(NC(NC3=CC(C(F)(F)F)=C(Cl)C=C3)=O)C=C2)=CC=N1 |
Canonical Smiles |
CNC(=O)C1=NC=CC(=C1)OC2=CC=C(C=C2)NC(=O)NC3=CC(=C(C=C3)Cl)C(F)(F)F |
InchIKey |
MLDQJTXFUGDVEO-FIBGUPNXSA-N |
Inchl |
InChI=1S/C21H16ClF3N4O3/c1-26-19(30)18-11-15(8-9-27-18)32-14-5-2-12(3-6-14)28-20(31)29-13-4-7-17(22)16(10-13)21(23,24)25/h2-11H,1H3,(H,26,30)(H2,28,29,31)/i1D3 |
IUPAC |
4-[4-[[4-chloro-3-(trifluoromethyl)phenyl]carbamoylamino]phenoxy]-N-(trideuteriomethyl)pyridine-2-carboxamide |
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.
Sorafenib D3 is a chemical compound that is commonly used as a targeted therapy for cancer treatment. It is a derivative of Sorafenib, which is an FDA-approved drug used to treat kidney, liver, and thyroid cancers. Sorafenib D3 is a deuterated form of Sorafenib, meaning that it contains three deuterium atoms in place of three hydrogen atoms in its chemical structure. This modification results in improved pharmacokinetic properties, which can lead to better efficacy and safety of the drug.
The mechanism of action of Sorafenib D3 involves inhibition of several protein kinases involved in cancer cell proliferation and angiogenesis. It prevents the growth of tumor cells by blocking the activity of a protein called RAF kinase, which is involved in cell signaling pathways that promote cancer cell growth. Additionally, Sorafenib D3 inhibits the activity of vascular endothelial growth factor receptors (VEGFRs) and platelet-derived growth factor receptors (PDGFRs), which are involved in the formation of new blood vessels that supply nutrients to cancer cells.
Sorafenib D3 is typically administered orally in the form of tablets or capsules. It is recommended to be taken on an empty stomach, either one hour before or two hours after a meal. The dosage and duration of treatment may vary depending on the type and stage of cancer being treated, as well as the patient's overall health and other medications being taken.
In conclusion, Sorafenib D3 is an effective targeted therapy for cancer treatment, with improved pharmacokinetic properties compared to its parent compound Sorafenib. Its mechanism of action involves inhibition of several protein kinases involved in cancer cell proliferation and angiogenesis. It is typically administered orally, and the dosage and duration of treatment may vary depending on the specific cancer being treated and the patient's individual needs.