(R)-5-Chloro-N-(2-hydroxy-3-((4-(3-oxomorpholino)phenyl)amino)propyl)thiophene-2-carboxamide

97%

Reagent Code: #230532
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CAS Number 721401-53-2

science Other reagents with same CAS 721401-53-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 409.89 g/mol
Formula C₁₈H₂₀ClN₃O₄S
badge Registry Numbers
MDL Number MFCD26227280
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used in the treatment of chronic inflammatory diseases, particularly rheumatoid arthritis. It functions as a selective kinase inhibitor, modulating immune response by suppressing the activity of key signaling proteins involved in inflammation. Its structure allows targeted interaction with intracellular enzymes, reducing cytokine production and preventing joint damage. Due to its chiral specificity, the (R)-enantiomer shows higher potency and lower off-target effects compared to the racemic mixture. Employed in oral dosage forms, it offers improved bioavailability and sustained therapeutic action with once-daily administration.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5mg
10-20 days ฿1,940.00
25mg
10-20 days ฿6,410.00
100mg
10-20 days ฿21,360.00
(R)-5-Chloro-N-(2-hydroxy-3-((4-(3-oxomorpholino)phenyl)amino)propyl)thiophene-2-carboxamide
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Used in the treatment of chronic inflammatory diseases, particularly rheumatoid arthritis. It functions as a selective kinase inhibitor, modulating immune response by suppressing the activity of key signaling proteins involved in inflammation. Its structure allows targeted interaction with intracellular enzymes, reducing cytokine production and preventing joint damage. Due to its chiral specificity, the (R)-enantiomer shows higher potency and lower off-target effects compared to the racemic mixture. Empl

Used in the treatment of chronic inflammatory diseases, particularly rheumatoid arthritis. It functions as a selective kinase inhibitor, modulating immune response by suppressing the activity of key signaling proteins involved in inflammation. Its structure allows targeted interaction with intracellular enzymes, reducing cytokine production and preventing joint damage. Due to its chiral specificity, the (R)-enantiomer shows higher potency and lower off-target effects compared to the racemic mixture. Employed in oral dosage forms, it offers improved bioavailability and sustained therapeutic action with once-daily administration.

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