1H-Pyrazolo[3,4-d]pyrimidin-6-amine

≥95%

Reagent Code: #195559
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CAS Number 287177-82-6

science Other reagents with same CAS 287177-82-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 135.13 g/mol
Formula C₅H₅N₅
badge Registry Numbers
MDL Number MFCD11559009
thermostat Physical Properties
Boiling Point 482.4°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.612g/cm3
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly kinase inhibitors. It plays a role in developing drugs for cancer treatment due to its ability to mimic purine bases, allowing it to bind effectively to enzyme active sites. Commonly found in research targeting tyrosine kinases and cyclin-dependent kinases, it contributes to the modulation of cell signaling pathways involved in tumor growth and proliferation. Also utilized in the development of anti-inflammatory and antiviral compounds. Its scaffold is valued in medicinal chemistry for enabling structural modifications that enhance selectivity and potency in drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,630.00
inventory 250mg
10-20 days ฿9,580.00
inventory 1g
10-20 days ฿27,030.00
inventory 5g
10-20 days ฿75,950.00

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1H-Pyrazolo[3,4-d]pyrimidin-6-amine
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly kinase inhibitors. It plays a role in developing drugs for cancer treatment due to its ability to mimic purine bases, allowing it to bind effectively to enzyme active sites. Commonly found in research targeting tyrosine kinases and cyclin-dependent kinases, it contributes to the modulation of cell signaling pathways involved in tumor growth and proliferation. Also utilized in the development of anti-inflammatory and antiviral
Used as a key intermediate in the synthesis of pharmaceutical agents, particularly kinase inhibitors. It plays a role in developing drugs for cancer treatment due to its ability to mimic purine bases, allowing it to bind effectively to enzyme active sites. Commonly found in research targeting tyrosine kinases and cyclin-dependent kinases, it contributes to the modulation of cell signaling pathways involved in tumor growth and proliferation. Also utilized in the development of anti-inflammatory and antiviral compounds. Its scaffold is valued in medicinal chemistry for enabling structural modifications that enhance selectivity and potency in drug candidates.
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