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Linopirdine

Cat. No. M27722

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

Linopirdine Structure
Synonym:

DuP 996

Size Price Availability Quantity
5mg USD 100  USD100 In stock
10mg USD 160  USD160 In stock
25mg USD 315  USD315 In stock
50mg USD 490  USD490 In stock
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Quality Control & Documentation
Biological Activity

Linopirdine (DuP 996) is an orally active, selective M-type K+ current (IM; Kv7; KCNQ Channels) inhibitor with an IC50 of 2.4 μM. Linopirdine is a TRPV1 agonist. Linopirdine, a putative cognition enhancing agent, increases acetylcholine release in rat brain tissue.

Chemical Information
Molecular Weight 391.46
Formula C26H21N3O
CAS Number 105431-72-9
Form Solid
Solubility (25°C) DMSO 125 mg/mL (ultrasonic)
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] F S Babu, et al. Physiol Res. Linopirdine-supplemented resuscitation fluids reduce mortality in a model of ischemia-reperfusion injury induced acute respiratory distress syndrome

[2] Cristian Neacsu, et al. J Pharmacol Sci. The M-channel blocker linopirdine is an agonist of the capsaicin receptor TRPV1

[3] Christian Wolff, et al. Eur J Pharmacol. [3H]linopirdine binding to rat brain membranes is not relevant for M-channel interaction

[4] María E Gomez-Casati, et al. J Assoc Res Otolaryngol. Linopirdine blocks alpha9alpha10-containing nicotinic cholinergic receptors of cochlear hair cells

[5] D J Fontana, et al. Pharmacol Biochem Behav. Linopirdine (DuP 996) improves performance in several tests of learning and memory by modulation of cholinergic neurotransmission

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Keywords: Linopirdine, DuP 996 supplier, Potassium Channel, inhibitors, activators

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