N-[(1,3-dimethyl-1H-pyrazol-4-yl)methyl]-N-methyl-5-phenyl-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidine-2-carboxamide

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Reagent Code: #245773
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CAS Number 489410-37-9

science Other reagents with same CAS 489410-37-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 428.41 g/mol
Formula C₂₁H₁₉F₃N₆O
inventory_2 Storage & Handling
Density 1.37±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a starting material or intermediate in the development of drugs targeting the central nervous system, particularly in research on GABA-A receptors, which are involved in seizures, anxiety, and insomnia. This compound acts as a positive modulator of GABA-A receptors of subtypes α1, α2, α3, or α5 depending on the substructure, offering potential for development into sedatives or hypnotics that are more selective and have fewer side effects than benzodiazepines. In vitro and animal studies demonstrate anti-seizure and calming effects without severe respiratory inhibition, making it a key approach for designing safer and more effective new drugs.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿6,590.00
inventory 10mg
10-20 days ฿10,440.00
inventory 25mg
10-20 days ฿20,890.00

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N-[(1,3-dimethyl-1H-pyrazol-4-yl)methyl]-N-methyl-5-phenyl-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidine-2-carboxamide
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Used as a starting material or intermediate in the development of drugs targeting the central nervous system, particularly in research on GABA-A receptors, which are involved in seizures, anxiety, and insomnia. This compound acts as a positive modulator of GABA-A receptors of subtypes α1, α2, α3, or α5 depending on the substructure, offering potential for development into sedatives or hypnotics that are more selective and have fewer side effects than benzodiazepines. In vitro and animal studies demonstra

Used as a starting material or intermediate in the development of drugs targeting the central nervous system, particularly in research on GABA-A receptors, which are involved in seizures, anxiety, and insomnia. This compound acts as a positive modulator of GABA-A receptors of subtypes α1, α2, α3, or α5 depending on the substructure, offering potential for development into sedatives or hypnotics that are more selective and have fewer side effects than benzodiazepines. In vitro and animal studies demonstrate anti-seizure and calming effects without severe respiratory inhibition, making it a key approach for designing safer and more effective new drugs.

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