N-(5-((4-(1-cyclopropyl-1H-indol-3-yl)pyrimidin-2-yl)amino)-2-((2-(dimethylamino)ethyl)(methyl)amino)-4-methoxyphenyl)acrylamide mesylate

98%

Reagent Code: #214781
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CAS Number 2134096-06-1

science Other reagents with same CAS 2134096-06-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 621.757 g/mol
Formula C₃₁H₃₉N₇O₅S
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used in research as a potent and selective inhibitor of the epidermal growth factor receptor (EGFR), particularly effective against mutant forms associated with non-small cell lung cancer (NSCLC). Shows high activity against EGFR T790M and C797S mutations, which are linked to resistance to earlier generations of EGFR inhibitors. Enables the study of signaling pathways in cancer cells and supports the development of next-generation targeted therapies. Due to its ability to cross the blood-brain barrier, it is also investigated for treating brain metastases of lung cancer. Primarily utilized in preclinical studies for evaluating antitumor efficacy and pharmacokinetic profiles.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿15,300.00
inventory 10mg
10-20 days ฿24,480.00
inventory 25mg
10-20 days ฿42,840.00

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N-(5-((4-(1-cyclopropyl-1H-indol-3-yl)pyrimidin-2-yl)amino)-2-((2-(dimethylamino)ethyl)(methyl)amino)-4-methoxyphenyl)acrylamide mesylate
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Used in research as a potent and selective inhibitor of the epidermal growth factor receptor (EGFR), particularly effective against mutant forms associated with non-small cell lung cancer (NSCLC). Shows high activity against EGFR T790M and C797S mutations, which are linked to resistance to earlier generations of EGFR inhibitors. Enables the study of signaling pathways in cancer cells and supports the development of next-generation targeted therapies. Due to its ability to cross the blood-brain barrier, i

Used in research as a potent and selective inhibitor of the epidermal growth factor receptor (EGFR), particularly effective against mutant forms associated with non-small cell lung cancer (NSCLC). Shows high activity against EGFR T790M and C797S mutations, which are linked to resistance to earlier generations of EGFR inhibitors. Enables the study of signaling pathways in cancer cells and supports the development of next-generation targeted therapies. Due to its ability to cross the blood-brain barrier, it is also investigated for treating brain metastases of lung cancer. Primarily utilized in preclinical studies for evaluating antitumor efficacy and pharmacokinetic profiles.

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