Shanghai Nianxing Industrial Co., Ltd
China
Product Name: LY344864 HCl
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Purity: 98.0%
Stocking Period: 10 Day
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1217756-94-9

1217756-94-9 structure

1217756-94-9 structure

Name: LY344864 HCl
Chemical Name: LY 344864 hydrochloride
CAS Number: 1217756-94-9
Molecular Formula: C₂₁H₂₃ClFN₃O
Molecular Weight: 387.88
Catalog: Signaling Pathways GPCR/G Protein 5-HT Receptor
Create Date: 2019-02-08 17:32:46
Modify Date: 2024-01-04 17:01:55
LY 344864 hydrochloride is a selective 5-HT1F agonist with a Ki of 6 nM.

Name	LY 344864 hydrochloride

Description	LY 344864 hydrochloride is a selective 5-HT1F agonist with a Ki of 6 nM.
Related Catalog	Signaling Pathways >> GPCR/G Protein >> 5-HT Receptor Signaling Pathways >> Neuronal Signaling >> 5-HT Receptor Research Areas >> Neurological Disease
Target	5-HT1F Receptor:6 nM (Ki)
In Vitro	LY344864 is a selective receptor agonist with an affinity of 6 nM (Ki) at the recently cloned 5-HT1F receptor. It possesses little affinity for the 56 other serotonergic and non-serotonergic neuronal binding sites examined. When examined for its ability to inhibit forskolininduced cyclic AMP accumulation in cells stably transfected with human 5-HT1F receptors, LY344864 is shown to be a full agonist producing an effect similar in magnitude to serotonin itself[1].
In Vivo	After an intravenous dose of 1 mg/kg, rat plasma LY344864 levels decline with time whereas brain cortex levels remaine relatively constant for the first 6 hours after injection. Oral and intravenous LY344864 administration potently inhibit dural protein extravasation caused by electrical stimulation of the trigeminal ganglion in rats[1]. Co-injection of LY 344864 and systemically ineffective doses of METH significantly decreases preference scores and the rewarding properties of METH during the reinstatement phase. In addition, administration of LY 344864 has no effect on the acquisition of CPP in rats[2].
Animal Admin	Rats[2] Male albino Wistar rats are divided into different groups. Rats in the experimental LY344864 and sham groups receive LY 344864 (1 or 2 μg/5 μL; intracerebroventricular [i.c.v.]), vehicle (5 μl/rat i.c.v.), or saline (5 μl/rat i.c.v.) during the acquisition phase[2]
References	[1]. Phebus LA, et al. Characterization of LY344864 as a pharmacological tool to study 5-HT1F receptors: binding affinities, brain penetration and activity in the neurogenic dural inflammation model of migraine. Life Sci. 1997;61(21):2117-26. [2]. Shahidi S, et al. Intracerebroventricular microinjection of the 5-HT1F receptor agonist LY 344864 inhibits methamphetamine conditioned place preference reinstatement in rats. Pharmacol Biochem Behav. 2018 Aug 2.

Molecular Formula	C₂₁H₂₃ClFN₃O
Molecular Weight	387.88

RIDADR	NONH for all modes of transport