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LY266097 hydrochloride

Catalog No. T22947   CAS 172895-39-5
Synonyms: LY 266097 hydrochloride

LY266097 hydrochloride (LY 266097 hydrochloride) is an antagonist of 5-HT2 with pKis of 7.7, 9.8, and 7.6 for human 5-HT2A, 5-HT2B, and 5-HT2C and can be used in studies about depression.

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LY266097 hydrochloride Chemical Structure
LY266097 hydrochloride, CAS 172895-39-5
Pack Size Availability Price/USD Quantity
1 mg In stock $ 34.00
5 mg In stock $ 118.00
10 mg In stock $ 176.00
25 mg In stock $ 297.00
50 mg In stock $ 443.00
100 mg In stock $ 639.00
1 mL * 10 mM (in DMSO) In stock $ 139.00
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Purity: 99.63%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description LY266097 hydrochloride (LY 266097 hydrochloride) is an antagonist of 5-HT2 with pKis of 7.7, 9.8, and 7.6 for human 5-HT2A, 5-HT2B, and 5-HT2C and can be used in studies about depression.
Targets&IC50 5-HT2A receptor:7.7 (pKi), 5-HT2B receptor:9.8 (pKi), 5-HT2C receptor:7.6 (pKi)
In vivo In vivo electrophysiological recordings of ventral tegmental area (VTA) dopamine (DA) neurons, dorsal raphe nucleus (DRN) 5-HT neurons and pyramidal neurons in the medial prefrontal cortex (mPFC), and the hippocampus were conducted in anaesthetized Sprague-Dawley rats after the administration of 5-HT2B receptor ligands alone or in combination with the SSRI escitalopram. An escitalopram-induced decrease in DA, but not 5-HT firing activity, was rescued by 2-day co-administration of the selective 5-HT2B receptor antagonist LY266097. In the mPFC, 14-day escitalopram administration alone had no effect on pyramidal neuron firing and burst activity, whereas, aripiprazole administered alone or in combination with escitalopram for 14 days increased pyramidal neuron firing and burst activity. Likewise, the administration of LY266097 alone or its addition on the last 3 days of a 14-day escitalopram regimen increased pyramidal neuron firing and burst activity[1].
Synonyms LY 266097 hydrochloride
Molecular Weight 407.33
Formula C21H24Cl2N2O2
CAS No. 172895-39-5

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 56.2 mg/mL (138.1 mM), Sonication and heating to 60℃ are recommended.

TargetMolReferences and Literature

1. Rami Hamati, et al. Serotonin-2B receptor antagonism increases the activity of dopamine and glutamate neurons in the presence of selective serotonin reuptake inhibition. Neuropsychopharmacology. 2020 Nov;45(12):2098-2105. 2. Luc Maroteaux, et al. New therapeutic opportunities for 5-HT 2 receptor ligands. Pharmacol Ther. 2017 Feb;170:14-36.

Related compound libraries

This product is contained In the following compound libraries:
Membrane Protein-targeted Compound Library GPCR Compound Library Bioactive Compound Library Neurotransmitter Receptor Compound Library Bioactive Compounds Library Max Neuronal Signaling Compound Library

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Related compounds with same targets
Pheniramine maleate Enciprazine Alosetron hydrochloride AL 34662 2-Methyl-5-HT hydrochloride Org 13011 SCH-23390 maleate Latrepirdine dihydrochloride

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Keywords

LY266097 hydrochloride 172895-39-5 GPCR/G Protein Neuroscience 5-HT Receptor LY 266097 Hydrochloride LY-266097 hydrochloride LY 266097 hydrochloride LY-266097 Hydrochloride LY266097 Hydrochloride inhibitor inhibit

 

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