CAS 1609392-27-9
:Deucravacitinib
Description:
Deucravacitinib is a novel small molecule that functions as a selective inhibitor of the enzyme tyrosine kinase 2 (TYK2), which plays a crucial role in the signaling pathways of various cytokines involved in immune responses. This compound is primarily investigated for its therapeutic potential in treating autoimmune diseases, particularly psoriasis and other inflammatory conditions. Deucravacitinib exhibits a unique mechanism of action by selectively targeting TYK2, thereby modulating the immune response with potentially fewer side effects compared to broader immunosuppressants. Its pharmacokinetic profile suggests good oral bioavailability and a favorable half-life, allowing for convenient dosing regimens. The substance is characterized by its specific chemical structure, which contributes to its selectivity and efficacy. Ongoing clinical trials are assessing its safety, tolerability, and effectiveness in various patient populations, making it a promising candidate in the field of immunology and dermatology. As research progresses, further insights into its long-term effects and potential applications in other diseases may emerge.
Formula:C20H22N8O3
Synonyms:- Deucravacitinib BMS986165
- 6-(cyclopropanecarboxamido)-4-((2-methoxy-3-(1-methyl-1H-1,2,4-triazol-3-yl) phenyl)amino)-N-(methyl-d3)pyridazine-3-carboxamide
- 6-cyclopropaneamido-4-{[2-methoxy-3-(1-methyl-1H-1,2,4-triazol-3-yl)phenyl]amino}-N-(2H?)methylpyridazine-3-carboxamide
- BMS-986165
- Tyk2-IN-4
- Deucravacitinib (TYK2-IN-4
- Deucravacitinib
- TYK2-IN-4;BMS986165;BMS-986165;BMS 986165
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 6 products.
Deucravacitinib
CAS:Deucravacitinib (BMS-986165) is a highly selective, orally bioavailable, allosteric TYK2 inhibitor.Cost-effective and quality-assured.Formula:C20H19D3N8O3Purity:98.52% - >99.99%Color and Shape:SolidMolecular weight:425.46Deucravacitinib
CAS:Controlled ProductFormula:C20D3H19N8O3Color and Shape:NeatMolecular weight:425.459BMS-986165
CAS:Controlled ProductBMS-986165 is a P-glycoprotein (P-gp) inhibitor that has been shown to reduce the absorption of ciclosporin, tacrolimus, and everolimus in vitro. BMS-986165 has an activity index of 100% and inhibits the inflammatory response by inhibiting the production of cytokines. It has been found to be effective for treating bowel diseases, such as ulcerative colitis and Crohn's disease. The drug also may be used for the treatment of autoimmune diseases, such as psoriasis or rheumatoid arthritis. BMS-986165 is administered orally and is rapidly absorbed. It is metabolized by CYP3A4 and excreted in urine as metabolites. END>> END>>Formula:C20H19D3N8O3Purity:Min. 95%Molecular weight:425.46 g/mol





