3-(4-(2-(3-(4-Chlorophenyl)-1,2,4-oxadiazol-5-yl)-2-(4-methoxyphenyl)ethyl)phenyl)isoxazole-5-carboxylic acid

95%

Reagent Code: #161819
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CAS Number 1373156-28-5

science Other reagents with same CAS 1373156-28-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 501.92 g/mol
Formula C₂₇H₂₀ClN₃O₅
badge Registry Numbers
MDL Number MFCD30532678
thermostat Physical Properties
Boiling Point 733.2±70.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used in pharmaceutical research as a potent and selective antagonist of the GPR139 receptor, which is implicated in neurological and psychiatric disorders. Shows potential in the development of treatments for conditions such as schizophrenia, depression, and Parkinson’s disease due to its ability to modulate dopaminergic and serotonergic pathways. Its carboxylic acid group allows for salt formation, improving solubility and bioavailability in preclinical studies. Also employed as a biochemical tool to investigate GPR139 receptor function in cellular and animal models.

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inventory 50mg
10-20 days ฿27,800.00

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3-(4-(2-(3-(4-Chlorophenyl)-1,2,4-oxadiazol-5-yl)-2-(4-methoxyphenyl)ethyl)phenyl)isoxazole-5-carboxylic acid
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Used in pharmaceutical research as a potent and selective antagonist of the GPR139 receptor, which is implicated in neurological and psychiatric disorders. Shows potential in the development of treatments for conditions such as schizophrenia, depression, and Parkinson’s disease due to its ability to modulate dopaminergic and serotonergic pathways. Its carboxylic acid group allows for salt formation, improving solubility and bioavailability in preclinical studies. Also employed as a biochemical tool to in

Used in pharmaceutical research as a potent and selective antagonist of the GPR139 receptor, which is implicated in neurological and psychiatric disorders. Shows potential in the development of treatments for conditions such as schizophrenia, depression, and Parkinson’s disease due to its ability to modulate dopaminergic and serotonergic pathways. Its carboxylic acid group allows for salt formation, improving solubility and bioavailability in preclinical studies. Also employed as a biochemical tool to investigate GPR139 receptor function in cellular and animal models.

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