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JNJ-61432059

SKU: orb1308172

Description

JNJ-61432059 is a potent, orally bioavailable, and selective negative allosteric modulator of TARP γ‑8-associated AMPA receptors (pIC50 = 9.7). This compound is a valuable research tool for investigating AMPA receptor function in neurological disorders and has demonstrated utility in both in vitro assays and in vivo preclinical models.

Research Area

Neuroscience, Pharmacology & Drug Discovery

Images & Validation

Key Properties

CAS Number2035814-50-5
MW443.47
Purity98.13%
FormulaC25H22FN5O2
SMILESOC1CCN(CC1)c1nccc2c(c(nn12)-c1ccc(F)cc1)-c1ccc2NC(=O)Cc2c1
TargetiGluR
SolubilityDMSO:65 mg/mL (146.57 mM);10% DMSO+40% PEG300+5% Tween 80+45% Saline:2 mg/mL (4.51 mM)

Bioactivity

Target IC50
AMPAR:(pic50)9.7
In Vivo
In mouse hippocampus, Exhibits time- and dose-dependent AMPAR/γ-8 receptor occupancy, resulting in robust seizure protection in corneal kindling and pentylenetetrazole (PTZ) anticonvulsant models.

Storage & Handling

StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

AMPAR, inhibit, Ionotropic glutamate receptors, JNJ 61432059, JNJ61432059, JNJ-61432059, iGluR, Inhibitor

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  • JNJ-61432059 [orb1940717]

    >98% (HPLC)

    2035814-50-5

    443.482

    C25H22FN5O2

    1 g, 50 mg, 100 mg, 5 mg, 10 mg, 25 mg, 500 mg
Quality Guarantee

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Key Properties

No computed properties available.

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JNJ-61432059 (orb1308172)

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% DMSO +
%+
% Tween 80 +
%

Available Sizes

Select a size below

1 mg
$ 150.00
5 mg
$ 290.00
1 ml x 10 mM (in DMSO)
$ 320.00
10 mg
$ 400.00
25 mg
$ 640.00
50 mg
$ 830.00
100 mg
$ 1,090.00
200 mg
$ 1,460.00
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