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Tau-aggregation and neuroinflammation-IN-1

🥰Excellent
Catalog No. T62899Cas No. 2175953-98-5

Tau-aggregation and neuroinflammation-IN-1 is a potent inhibitor of tau protein aggregates, showing significant inhibitory activity against AcPHF6 and full-length tau protein aggregates. It has anti-inflammatory activity, reduces NO release, exhibits low cytotoxicity against LSP-stimulated BV2 cells, and reverses okadaic acid-induced memory impairment in rats.

Tau-aggregation and neuroinflammation-IN-1

Tau-aggregation and neuroinflammation-IN-1

🥰Excellent
Purity: 100%
Catalog No. T62899Cas No. 2175953-98-5
Tau-aggregation and neuroinflammation-IN-1 is a potent inhibitor of tau protein aggregates, showing significant inhibitory activity against AcPHF6 and full-length tau protein aggregates. It has anti-inflammatory activity, reduces NO release, exhibits low cytotoxicity against LSP-stimulated BV2 cells, and reverses okadaic acid-induced memory impairment in rats.
Pack SizePriceAvailabilityQuantity
5 mg$39In Stock
10 mg$64In Stock
25 mg$122In Stock
50 mg$197In Stock
100 mg$293In Stock
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Purity:100%
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Product Introduction

Bioactivity
Description
Tau-aggregation and neuroinflammation-IN-1 is a potent inhibitor of tau protein aggregates, showing significant inhibitory activity against AcPHF6 and full-length tau protein aggregates. It has anti-inflammatory activity, reduces NO release, exhibits low cytotoxicity against LSP-stimulated BV2 cells, and reverses okadaic acid-induced memory impairment in rats.
In vitro
Tau-aggregation and neuroinflammation-IN-1 (compound 30) (0-40 μM) reduces the survival of SH-SY5Y cells at 30 μM and exhibits no significant hepatotoxicity at high concentrations in LO2 cells, without affecting the viability of BV2 cells at 20 μM. Tau-aggregation and neuroinflammation-IN-1 (2.5, 5, and 10 μM; 24 h) maintain the anti-inflammatory effect of sodium usage and decrease the NO release rate by 41% at 10 μM in LPS-stimulated BV2 cells.[1]
In vivo
Tau-aggregation and neuroinflammation-IN-1 (5 and 10 mg/kg; I.P.; for 7 days, followed by 7 additional days post-OA injection; Male SD rats) significantly enhances spatial memory and cognitive abilities in OA-induced rats.[1]
Chemical Properties
Molecular Weight460.44
FormulaC25H20N2O7
Cas No.2175953-98-5
SmilesC[C@@]12C=3C(OC1=CC4=C(C2=O)C(C)=NN4C5=CC=C(C(O)=O)C=C5)=C(C(C)=O)C(O)=C(C)C3O
Storage & Solubility Information
StorageShipping with blue ice.
Solubility Information
DMSO: 50 mg/mL (108.59 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.1718 mL10.8592 mL21.7184 mL108.5918 mL
5 mM0.4344 mL2.1718 mL4.3437 mL21.7184 mL
10 mM0.2172 mL1.0859 mL2.1718 mL10.8592 mL
20 mM0.1086 mL0.5430 mL1.0859 mL5.4296 mL
50 mM0.0434 mL0.2172 mL0.4344 mL2.1718 mL
100 mM0.0217 mL0.1086 mL0.2172 mL1.0859 mL

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