6-O-Nicotinoylscutebarbatine G

95%

Reagent Code: #221820
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CAS Number 1206805-30-2

science Other reagents with same CAS 1206805-30-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 576.64 g/mol
Formula C₃₂H₃₆N₂O₈
inventory_2 Storage & Handling
Density 1.35±0.1g/ml
Storage 2-8℃, dry, closed

description Product Description

Used in research for its potential neuroprotective properties, particularly in models of oxidative stress and neuronal damage. Shows activity as a nicotinic acetylcholine receptor modulator, suggesting possible applications in neurodegenerative disease studies such as Alzheimer's and Parkinson's. Also investigated for anti-inflammatory effects in cellular assays, indicating utility in developing therapies for chronic inflammatory conditions. Its natural origin and structural complexity make it a candidate for structure-activity relationship (SAR) studies in alkaloid-based drug design.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5mg
10-20 days ฿30,010.00
6-O-Nicotinoylscutebarbatine G
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Used in research for its potential neuroprotective properties, particularly in models of oxidative stress and neuronal damage. Shows activity as a nicotinic acetylcholine receptor modulator, suggesting possible applications in neurodegenerative disease studies such as Alzheimer's and Parkinson's. Also investigated for anti-inflammatory effects in cellular assays, indicating utility in developing therapies for chronic inflammatory conditions. Its natural origin and structural complexity make it a candidat

Used in research for its potential neuroprotective properties, particularly in models of oxidative stress and neuronal damage. Shows activity as a nicotinic acetylcholine receptor modulator, suggesting possible applications in neurodegenerative disease studies such as Alzheimer's and Parkinson's. Also investigated for anti-inflammatory effects in cellular assays, indicating utility in developing therapies for chronic inflammatory conditions. Its natural origin and structural complexity make it a candidate for structure-activity relationship (SAR) studies in alkaloid-based drug design.

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