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Idalopirdine hydrochloride

Cat. No. M9025

All AbMole products are for research use only, cannot be used for human consumption.

Idalopirdine hydrochloride Structure
Synonym:

Lu AE58054 HCl

Size Price Availability Quantity
1mg USD 110 In stock
2mg USD 180 In stock
5mg USD 240 In stock
10mg USD 340 In stock
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Quality Control & Documentation
Biological Activity

Idalopirdine hydrochloride displayed high affinity to the human 5-HT(6) receptor (5-HT(6)R) with a Ki of 0.83 nm. In vivo, orally administered Idalopirdine hcl potently inhibited striatal in-vivo binding of the 5-HT(6) antagonist radioligand [(3)H]Lu AE60157, with an ED(50) of 2.7 mg/kg.

Chemical Information
Molecular Weight 434.83
Formula C20H20ClF5N2O
CAS Number 467458-02-2
Solubility (25°C) DMSO: ≥ 20 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Witten L, et al. Eur J Pharmacol. Characterization of [³H]Lu AE60157 ([³H]8-(4-methylpiperazin-1-yl)-3-phenylsulfonylquinoline) binding to 5-hydroxytryptamine₆ (5-HT₆) receptors in vivo.

[2] Arnt J, et al. Int J Neuropsychopharmacol. Lu AE58054, a 5-HT6 antagonist, reverses cognitive impairment induced by subchronic phencyclidine in a novel object recognition test in rats.

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Keywords: Idalopirdine hydrochloride, Lu AE58054 HCl supplier, 5-HT Receptor, inhibitors, activators

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