Ozanimod (RPC1063)

10mM in DMSO

Reagent Code: #221215
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CAS Number 1306760-87-1

science Other reagents with same CAS 1306760-87-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 404.46 g/mol
Formula C₂₃H₂₄N₄O₃
badge Registry Numbers
MDL Number MFCD28386168
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Ozanimod is primarily used in the treatment of multiple sclerosis (MS), specifically for relapsing forms of the disease, including relapsing-remitting MS. It helps reduce the frequency of clinical relapses and slows the accumulation of physical disability. The drug also shows efficacy in managing moderately to severely active ulcerative colitis, an inflammatory bowel disease. By modulating the immune system—specifically through selective targeting of sphingosine 1-phosphate receptors—it reduces the migration of lymphocytes into inflamed tissues, thereby decreasing inflammation and autoimmune activity. Its oral formulation offers a convenient dosing option compared to injectable therapies, improving patient adherence. Due to its targeted mechanism, it has a favorable safety profile with fewer cardiovascular and hepatic side effects compared to earlier non-selective agents.

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inventory 1ml
10-20 days ฿3,680.00

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Ozanimod (RPC1063)
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Ozanimod is primarily used in the treatment of multiple sclerosis (MS), specifically for relapsing forms of the disease, including relapsing-remitting MS. It helps reduce the frequency of clinical relapses and slows the accumulation of physical disability. The drug also shows efficacy in managing moderately to severely active ulcerative colitis, an inflammatory bowel disease. By modulating the immune system—specifically through selective targeting of sphingosine 1-phosphate receptors—it reduces the migration of lymphocytes into inflamed tissues, thereby decreasing inflammation and autoimmune activity. Its oral formulation offers a convenient dosing option compared to injectable therapies, improving patient adherence. Due to its targeted mechanism, it has a favorable safety profile with fewer cardiovascular and hepatic side effects compared to earlier non-selective agents.
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