Comparison

Ansofaxine hydrochloride

Item no. CS-7132-100mg
Manufacturer ChemScene
Amount 100mg
Category
Type Molecules
Specific against other
ECLASS 10.1 32169090
ECLASS 11.0 32169090
UNSPSC 12000000
Alias 916918-84-8
Similar products 916918-84-8
Available
Alternative Names
LY03005; LPM570065
CAS
916918-84-8
Purity
>98%
MWt
417.97
Formula
C24H32ClNO3
Solubility
DMSO : 31.25 mg/mL (74.77 mM; Need ultrasonic)
Clinical Information
Phase 1
Pathway
GPCR/G Protein; Neuronal Signaling; Neuronal Signaling; GPCR/G Protein
Target
Dopamine Receptor; Dopamine Receptor; 5-HT Receptor; 5-HT Receptor
Biological Activity
Ansofaxine hydrochloride (LY03005; LPM570065) is a triple reuptake inhibitor; inhibits serotonin, dopamine and norepinephrine reuptake with IC50 values of 723, 491 and 763 nM, respectively. IC50 & Target: IC50: 723 nM (serotonin), 491 nM (dopamine), 763 nM (norepinephrine)[1] In Vivo: Ansofaxine rapidly penetrates the rat striatum, converts into desvenlafaxine and exhibits larger total exposure compared with the administration of desvenlafaxine. Acute and chronic administration of oral suspension of ansofaxine increases the 5-HT, dopamine and norepinephrine levels more than the relative administration of desvenlafaxine. Unlike desvenlafaxine, acute administration of an intravenous ansofaxine solution does not induce the undesirable 90% decrease in extracellular 5-HT levels. The acute administration of ansofaxine shows a capped increase in extracellular 5-HT levels when combined with WAY-100635. Acute and chronic administration of ansofaxine reduces the immobility time more than the relative administration of desvenlafaxine[1].
Research Area
Inflammation/Immunology; Neurological Disease

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Amount: 100mg
Available: In stock
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