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A-804598

SKU: orb1223426

Description

A-804598 is a competitive and selective P2X7 receptor antagonist (IC50: 10 nM, rat; 9 nM, mouse; 11 nM, human).

Images & Validation

Key Properties

CAS Number1125758-85-1
MW315.37
Purity>98% (HPLC)
FormulaC19H17N5
SMILESC[C@@H](c1ccccc1)N=C(NC#N)Nc1cccc2c1cccn2
TargetMAO
SolubilityDMSO : ≥ 32 mg/mL 101.47 mM

Bioactivity

In Vivo
A chroni treatment with A-804598 (intraperitoneal injection; 30 mg/kg; five times a week) decreases the expression of LC3B-II and SQSTM1/p62 in lumbar spinal cord at end stage of disease. Animal model: Adult B6.Cg-Tg (SOD1-G93A) 1Gur/J female mice. Dosage: 30 mg/kg. Administration: Intraperitoneal injection; five times a week. Result: Decreased SQSTM1/p62 expression.
In Vitro
Pre-incubation with A-804598 (0.1-10 μM; 1 hour) significantly attenuates BzATP-induced cell loss in a concentration-dependent manner. 3 μM A-804598 exhibits the greatest protective effect against BzATP-induced cytotoxicity. Cell Cytotoxicity Assay Cell line: microglial cell. Concentration: 0.1, 0.3, 1, 3, 10 μM Incubation time: 1 hour. Result: Protected against BzATP-induced cytotoxicity in both inactivated and activated microglia.

Storage & Handling

StorageStorage temperature: -20°C. Stability: ≥ 2 years
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

A-804598 | A 804598 | A804598.

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  • A-804598 [orb1303970]

    >99.99% (May vary between batches)

    1125758-85-1

    315.37

    C19H17N5

    2 mg, 10 mg, 500 mg, 1 ml x 10 mM (in DMSO), 100 mg, 5 mg, 25 mg, 50 mg
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Protocol Information

A-804598 (orb1223426)

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Step 1: Enter information below

(Recommended: An additional animal making an allowance for loss during the experiment)

Step 2: Enter the in vivo formulation

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% DMSO +
%+
% Tween 80 +
%

Available Sizes

Select a size below

2 mg
$ 80.00
5 mg
$ 110.00
10 mg
$ 140.00
25 mg
$ 270.00
50 mg
$ 440.00
100 mg
$ 700.00
500 mg
$ 1,520.00