2-Cyclobutyl-10-methyl-3-phenylpyrimido[4,5-b]quinoline-4,5(3H,10H)-dione

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Reagent Code: #157165
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CAS Number 1613509-49-1

science Other reagents with same CAS 1613509-49-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 357.4052 g/mol
Formula C₂₂H₁₉N₃O₂
thermostat Physical Properties
Boiling Point 495.3±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.35±0.1 g/cm3(Predicted)
Storage -20°C

description Product Description

Used in research as a potent inhibitor of cyclin-dependent kinases (CDKs), particularly CDK2 and CDK4, making it valuable in studies related to cell cycle regulation and cancer development. Shows promise in preclinical models for antitumor activity due to its ability to induce cell cycle arrest and apoptosis in cancer cells. Also employed as a molecular probe to investigate signaling pathways involved in proliferation and transcription. Its selective kinase inhibition profile supports its use in developing targeted cancer therapies.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿12,800.00
inventory 25mg
10-20 days ฿16,000.00
inventory 100mg
10-20 days ฿40,000.00
inventory 1g
10-20 days ฿160,000.00

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2-Cyclobutyl-10-methyl-3-phenylpyrimido[4,5-b]quinoline-4,5(3H,10H)-dione
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Used in research as a potent inhibitor of cyclin-dependent kinases (CDKs), particularly CDK2 and CDK4, making it valuable in studies related to cell cycle regulation and cancer development. Shows promise in preclinical models for antitumor activity due to its ability to induce cell cycle arrest and apoptosis in cancer cells. Also employed as a molecular probe to investigate signaling pathways involved in proliferation and transcription. Its selective kinase inhibition profile supports its use in developi

Used in research as a potent inhibitor of cyclin-dependent kinases (CDKs), particularly CDK2 and CDK4, making it valuable in studies related to cell cycle regulation and cancer development. Shows promise in preclinical models for antitumor activity due to its ability to induce cell cycle arrest and apoptosis in cancer cells. Also employed as a molecular probe to investigate signaling pathways involved in proliferation and transcription. Its selective kinase inhibition profile supports its use in developing targeted cancer therapies.

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