N-(2-(1H-Benzo[d]imidazol-2-yl)phenyl)-3,4,5-trimethoxybenzamide

98%

Reagent Code: #215616
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CAS Number 313275-18-2

science Other reagents with same CAS 313275-18-2

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Weight 403.43 g/mol
Formula C₂₃H₂₁N₃O₄
inventory_2 Storage & Handling
Density 1.296±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used in pharmaceutical research as a key scaffold in the development of kinase inhibitors, particularly targeting cyclin-dependent kinases (CDKs) involved in cell cycle regulation. Shows potential in anticancer drug design due to its ability to induce apoptosis and inhibit tumor cell proliferation. Also investigated for anti-inflammatory and antimicrobial properties, leveraging its benzimidazole core for interaction with biological targets. Employed in structure-activity relationship (SAR) studies to optimize potency and selectivity in drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿26,690.00
inventory 250mg
10-20 days ฿45,370.00

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N-(2-(1H-Benzo[d]imidazol-2-yl)phenyl)-3,4,5-trimethoxybenzamide
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Used in pharmaceutical research as a key scaffold in the development of kinase inhibitors, particularly targeting cyclin-dependent kinases (CDKs) involved in cell cycle regulation. Shows potential in anticancer drug design due to its ability to induce apoptosis and inhibit tumor cell proliferation. Also investigated for anti-inflammatory and antimicrobial properties, leveraging its benzimidazole core for interaction with biological targets. Employed in structure-activity relationship (SAR) studies to opt

Used in pharmaceutical research as a key scaffold in the development of kinase inhibitors, particularly targeting cyclin-dependent kinases (CDKs) involved in cell cycle regulation. Shows potential in anticancer drug design due to its ability to induce apoptosis and inhibit tumor cell proliferation. Also investigated for anti-inflammatory and antimicrobial properties, leveraging its benzimidazole core for interaction with biological targets. Employed in structure-activity relationship (SAR) studies to optimize potency and selectivity in drug candidates.

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