4-Amino-2-butoxy-8-[4-(1-pyrrolidinylmethyl)benzyl]-7,8-dihydro-6(5H)-pteridinone

≥95%

Reagent Code: #137520
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CAS Number 1228585-41-8

science Other reagents with same CAS 1228585-41-8

blur_circular Chemical Specifications

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Weight 410.51 g/mol
Formula C₂₂H₃₀N₆O₂
inventory_2 Storage & Handling
Storage Room temperature

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Used primarily in pharmaceutical research as a key intermediate in the synthesis of selective kinase inhibitors. It shows particular relevance in the development of targeted cancer therapies, where it helps modulate signaling pathways involved in cell proliferation and survival. Its structure allows for strong binding affinity to specific enzyme active sites, making it valuable in optimizing drug candidates for improved potency and selectivity. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance metabolic stability and bioavailability in lead compounds.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿13,110.00
inventory 5mg
10-20 days ฿39,140.00

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4-Amino-2-butoxy-8-[4-(1-pyrrolidinylmethyl)benzyl]-7,8-dihydro-6(5H)-pteridinone
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Used primarily in pharmaceutical research as a key intermediate in the synthesis of selective kinase inhibitors. It shows particular relevance in the development of targeted cancer therapies, where it helps modulate signaling pathways involved in cell proliferation and survival. Its structure allows for strong binding affinity to specific enzyme active sites, making it valuable in optimizing drug candidates for improved potency and selectivity. Also employed in medicinal chemistry for structure-activity

Used primarily in pharmaceutical research as a key intermediate in the synthesis of selective kinase inhibitors. It shows particular relevance in the development of targeted cancer therapies, where it helps modulate signaling pathways involved in cell proliferation and survival. Its structure allows for strong binding affinity to specific enzyme active sites, making it valuable in optimizing drug candidates for improved potency and selectivity. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance metabolic stability and bioavailability in lead compounds.

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