(4-(3-Chlorophenyl)piperazin-1-yl)(2-(3,4-dimethoxyphenyl)quinolin-4-yl)methanone

98%

Reagent Code: #156839
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CAS Number 544662-95-5

science Other reagents with same CAS 544662-95-5

blur_circular Chemical Specifications

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Weight 487.98 g/mol
Formula C₂₈H₂₆ClN₃O₃
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in research as a potent and selective antagonist for serotonin receptors, particularly 5-HT2A, making it valuable in neuroscience studies related to mood, perception, and psychiatric disorders. It serves as a pharmacological tool to investigate the role of serotonergic signaling in behavioral models and is also employed in the development of novel CNS-active compounds. Its structural features support binding affinity and selectivity, enabling detailed structure-activity relationship (SAR) studies in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,480.00
inventory 250mg
10-20 days ฿28,020.00
inventory 1g
10-20 days ฿75,630.00

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(4-(3-Chlorophenyl)piperazin-1-yl)(2-(3,4-dimethoxyphenyl)quinolin-4-yl)methanone
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Used in research as a potent and selective antagonist for serotonin receptors, particularly 5-HT2A, making it valuable in neuroscience studies related to mood, perception, and psychiatric disorders. It serves as a pharmacological tool to investigate the role of serotonergic signaling in behavioral models and is also employed in the development of novel CNS-active compounds. Its structural features support binding affinity and selectivity, enabling detailed structure-activity relationship (SAR) studies in

Used in research as a potent and selective antagonist for serotonin receptors, particularly 5-HT2A, making it valuable in neuroscience studies related to mood, perception, and psychiatric disorders. It serves as a pharmacological tool to investigate the role of serotonergic signaling in behavioral models and is also employed in the development of novel CNS-active compounds. Its structural features support binding affinity and selectivity, enabling detailed structure-activity relationship (SAR) studies in medicinal chemistry.

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