N-(Benzo[d][1,3]dioxol-5-yl)-2-((3-(furan-2-ylmethyl)-4-oxo-3,4-dihydroquinazolin-2-yl)thio)acetamide

98%

Reagent Code: #215817
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CAS Number 853351-76-5

science Other reagents with same CAS 853351-76-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 435.45 g/mol
Formula C₂₂H₁₇N₃O₅S
inventory_2 Storage & Handling
Density 1.48±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used in pharmaceutical research as a potential inhibitor of inflammatory and oncogenic pathways. Shows activity in modulating signaling proteins involved in cancer cell proliferation and apoptosis. Investigated for its antitumor properties, particularly in studies related to kinase inhibition and suppression of tumor growth in preclinical models. Also explored for anti-inflammatory effects due to structural features that interact with cellular targets like NF-κB and cytokine production pathways. Its furan and quinazoline moieties contribute to binding affinity with biological targets, making it a scaffold for developing new therapeutic agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿22,890.00
inventory 250mg
10-20 days ฿38,890.00

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N-(Benzo[d][1,3]dioxol-5-yl)-2-((3-(furan-2-ylmethyl)-4-oxo-3,4-dihydroquinazolin-2-yl)thio)acetamide
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Used in pharmaceutical research as a potential inhibitor of inflammatory and oncogenic pathways. Shows activity in modulating signaling proteins involved in cancer cell proliferation and apoptosis. Investigated for its antitumor properties, particularly in studies related to kinase inhibition and suppression of tumor growth in preclinical models. Also explored for anti-inflammatory effects due to structural features that interact with cellular targets like NF-κB and cytokine production pathways. Its fura

Used in pharmaceutical research as a potential inhibitor of inflammatory and oncogenic pathways. Shows activity in modulating signaling proteins involved in cancer cell proliferation and apoptosis. Investigated for its antitumor properties, particularly in studies related to kinase inhibition and suppression of tumor growth in preclinical models. Also explored for anti-inflammatory effects due to structural features that interact with cellular targets like NF-κB and cytokine production pathways. Its furan and quinazoline moieties contribute to binding affinity with biological targets, making it a scaffold for developing new therapeutic agents.

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