3-(2,5-dimethoxyphenyl)-2-thioxo-2,3-dihydro-4(1H)-quinazolinone

≥95%

Reagent Code: #197794
fingerprint
CAS Number 380436-98-6

science Other reagents with same CAS 380436-98-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 314.36 g/mol
Formula C₁₆H₁₄N₂O₃S
badge Registry Numbers
MDL Number MFCD01933667
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used in pharmaceutical research as a key scaffold for developing bioactive compounds, particularly in the design of CNS-targeted agents due to its affinity for serotonin and dopamine receptors. Shows potential in the synthesis of novel antipsychotic and antidepressant candidates. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies of quinazolinone derivatives. Its thioxo and methoxy substitutions enhance binding selectivity and metabolic stability, making it valuable in optimizing drug-like properties. Additionally, utilized in fluorescence-based assays owing to its inherent photophysical characteristics, supporting high-throughput screening in drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿7,380.00
$product.analytical_desc - NULL

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-(2,5-dimethoxyphenyl)-2-thioxo-2,3-dihydro-4(1H)-quinazolinone
No image available

Used in pharmaceutical research as a key scaffold for developing bioactive compounds, particularly in the design of CNS-targeted agents due to its affinity for serotonin and dopamine receptors. Shows potential in the synthesis of novel antipsychotic and antidepressant candidates. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies of quinazolinone derivatives. Its thioxo and methoxy substitutions enhance binding selectivity and metabolic stability, making it valuable in

Used in pharmaceutical research as a key scaffold for developing bioactive compounds, particularly in the design of CNS-targeted agents due to its affinity for serotonin and dopamine receptors. Shows potential in the synthesis of novel antipsychotic and antidepressant candidates. Also employed in medicinal chemistry for structure-activity relationship (SAR) studies of quinazolinone derivatives. Its thioxo and methoxy substitutions enhance binding selectivity and metabolic stability, making it valuable in optimizing drug-like properties. Additionally, utilized in fluorescence-based assays owing to its inherent photophysical characteristics, supporting high-throughput screening in drug discovery.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...