1-Cyclohexyl-N-(pyridin-3-ylmethyl)-2-(1-tosylpiperidin-4-yl)-1H-benzo[d]imidazole-5-carboxamide

95%

Reagent Code: #215728
fingerprint
CAS Number 898220-69-4

science Other reagents with same CAS 898220-69-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 571.73 g/mol
Formula C₃₂H₃₇N₅O₃S
inventory_2 Storage & Handling
Density 1.33±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used in pharmaceutical research as a potent and selective antagonist of the histamine H4 receptor, this compound is investigated for its anti-inflammatory and immunomodulatory effects. It shows potential in treating allergic diseases such as asthma and atopic dermatitis, as well as autoimmune conditions like rheumatoid arthritis. Due to its ability to cross the blood-brain barrier, it is also explored for central nervous system disorders involving neuroinflammation. Its structure allows for high receptor binding affinity and improved metabolic stability, making it a valuable scaffold in drug development targeting H4 receptor-mediated pathways.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1mg
10-20 days ฿14,100.00
1-Cyclohexyl-N-(pyridin-3-ylmethyl)-2-(1-tosylpiperidin-4-yl)-1H-benzo[d]imidazole-5-carboxamide
No image available
Used in pharmaceutical research as a potent and selective antagonist of the histamine H4 receptor, this compound is investigated for its anti-inflammatory and immunomodulatory effects. It shows potential in treating allergic diseases such as asthma and atopic dermatitis, as well as autoimmune conditions like rheumatoid arthritis. Due to its ability to cross the blood-brain barrier, it is also explored for central nervous system disorders involving neuroinflammation. Its structure allows for high receptor bi
Used in pharmaceutical research as a potent and selective antagonist of the histamine H4 receptor, this compound is investigated for its anti-inflammatory and immunomodulatory effects. It shows potential in treating allergic diseases such as asthma and atopic dermatitis, as well as autoimmune conditions like rheumatoid arthritis. Due to its ability to cross the blood-brain barrier, it is also explored for central nervous system disorders involving neuroinflammation. Its structure allows for high receptor binding affinity and improved metabolic stability, making it a valuable scaffold in drug development targeting H4 receptor-mediated pathways.
Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...