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Ansofaxine hydrochloride

Catalog No. T5380   CAS 916918-84-8
Synonyms: LPM570065, LY03005

Ansofaxine hydrochloride (LY03005) is a serotonin-norepinephrine-dopamine reuptake inhibitor (IC50s: 723, 763 and 491 nM, respectively).

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Ansofaxine hydrochloride Chemical Structure
Ansofaxine hydrochloride, CAS 916918-84-8
Pack Size Availability Price/USD Quantity
1 mg In stock $ 90.00
2 mg In stock $ 125.00
5 mg In stock $ 182.00
10 mg In stock $ 309.00
25 mg In stock $ 566.00
50 mg In stock $ 812.00
100 mg In stock $ 1,130.00
500 mg In stock $ 2,260.00
1 mL * 10 mM (in DMSO) In stock $ 197.00
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Purity: 99.63%
Purity: 99.63%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Ansofaxine hydrochloride (LY03005) is a serotonin-norepinephrine-dopamine reuptake inhibitor (IC50s: 723, 763 and 491 nM, respectively).
Targets&IC50 Norepinephrine:763 nM, Dopamine:491 nM, 5-HT:723 nM
In vivo Acute administration was performed by providing rodents with oral solutions (0.06 mmol/kg p.o.), oral suspensions (0.06 mmol/kg p.o.) and intravenous solutions (0.04 mmol/kg i.v.) of LPM570065 and desvenlafaxine. Oral suspensions (0.06 mmol/kg/day) of the two drugs were also administered for a 14-day chronic period. LPM570065 rapidly penetrated the rat striatum, converted into desvenlafaxine and exhibited larger total exposure compared with the administration of desvenlafaxine. Acute and chronic administration of oral suspension of LPM570065 increased the 5-HT, DA and NE levels more than the relative administration of desvenlafaxine [1]. The maximum tolerated dose (MTD) was 500?mg/kg and the lethal dose was 1000?mg/kg in SD rats after a single administration of LPM570065. In 13-week repeated-dose oral toxicity, the no-observed-adverse-effect level (NOAEL) of LPM570065 was greater than 300?mg/kg for rats [2].
Animal Research The dosages of LPM570065 and desvenlafaxine used with different administration routes referred to previous studies and was determined by preliminary experiments. Oral solutions of LPM570065 and desvenlafaxine for intragastric administration (0.06 mmol/kg p.o.) were prepared by dissolving the compounds in 10% glucose. Oral suspensions of LPM570065 and desvenlafaxine for intragastric administration (0.06 mmol/kg p.o.) were prepared by suspending the compounds in 0.5% carboxymethylcellulose sodium. Intravenous solutions of LPM570065 and desvenlafaxine for intravenous administration (0.04 mmol/kg i.v.) were prepared by dissolving the compounds in 10% glucose. WAY-100635 was dissolved in 0.9% saline and was administered subcutaneously (0.3 mg/kg s.c.). Raclopride was dissolved in 0.9% saline and was administered subcutaneously (0.5 mg/kg s.c.). Different vehicles were used for administration using different administration routes [1].
Synonyms LPM570065, LY03005
Molecular Weight 417.97
Formula C24H32ClNO3
CAS No. 916918-84-8

Storage

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

Solubility Information

DMSO: 30 mg/mL (71.77 mM)

TargetMolReferences and Literature

1. Zhang R, et al. The effects of LPM570065, a novel triple reuptake inhibitor, on extracellular serotonin, dopamineand norepinephrine levels in rats. PLoS One. 2014 Mar 10;9(3):e91775. 2. Li C, et al. Acute, subchronic oral toxicity, and genotoxicity evaluations of LPM570065, a new potent triple reuptake inhibitor. Regul Toxicol Pharmacol. 2018 Oct;98:129-139.

Related compound libraries

This product is contained In the following compound libraries:
Anti-Cancer Drug Library Drug Repurposing Compound Library Anti-Neurodegenerative Disease Compound Library Inhibitor Library Anti-Cancer Clinical Compound Library GPCR Compound Library Anti-Alzheimer's Disease Compound Library Bioactive Compound Library NO PAINS Compound Library Serotonin Receptor-Targeted Compound Library

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Keywords

Ansofaxine hydrochloride 916918-84-8 GPCR/G Protein Neuroscience Dopamine Receptor 5-HT Receptor Norepinephrine 5-hydroxytryptamine Receptor inhibit Ansofaxine Hydrochloride Serotonin Receptor LY 03005 LPM570065 Ansofaxine LPM 570065 Inhibitor LPM-570065 LY03005 LY-03005 inhibitor

 

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