N-[Benzo[1,3]dioxol-5-yl-(5-chloro-8-hydroxy-quinolin-7-yl)-methyl]-butyramide

98%

Reagent Code: #219436
fingerprint
CAS Number 423145-35-1

science Other reagents with same CAS 423145-35-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 398.846 g/mol
Formula C₂₁H₁₉ClN₂O₄
inventory_2 Storage & Handling
Storage -20°C, Sealed

description Product Description

Used in research as a potent inhibitor of specific enzymes involved in neurodegenerative diseases, particularly targeting beta-secretase (BACE1) for potential Alzheimer’s therapy. Shows high blood-brain barrier permeability, making it valuable in developing central nervous system-active drugs. Also serves as a scaffold in medicinal chemistry for optimizing quinoline-based compounds with anti-inflammatory and neuroprotective properties. Investigated for its role in reducing amyloid-beta plaque formation in preclinical models.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿2,500.00
inventory 25mg
10-20 days ฿8,630.00
inventory 50mg
10-20 days ฿12,940.00
inventory 100mg
10-20 days ฿20,210.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
N-[Benzo[1,3]dioxol-5-yl-(5-chloro-8-hydroxy-quinolin-7-yl)-methyl]-butyramide
No image available

Used in research as a potent inhibitor of specific enzymes involved in neurodegenerative diseases, particularly targeting beta-secretase (BACE1) for potential Alzheimer’s therapy. Shows high blood-brain barrier permeability, making it valuable in developing central nervous system-active drugs. Also serves as a scaffold in medicinal chemistry for optimizing quinoline-based compounds with anti-inflammatory and neuroprotective properties. Investigated for its role in reducing amyloid-beta plaque formation i

Used in research as a potent inhibitor of specific enzymes involved in neurodegenerative diseases, particularly targeting beta-secretase (BACE1) for potential Alzheimer’s therapy. Shows high blood-brain barrier permeability, making it valuable in developing central nervous system-active drugs. Also serves as a scaffold in medicinal chemistry for optimizing quinoline-based compounds with anti-inflammatory and neuroprotective properties. Investigated for its role in reducing amyloid-beta plaque formation in preclinical models.

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...