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OPC-14523 hydrochloride

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TargetMol
Catalog No. T62711Cas No. 145969-31-9
Alias VPI 013 hydrochloride

OPC-14523 hydrochloride is an orally active sigma and 5-HT1A receptor agonist with antidepressant-like activity, showing high affinity for the sigma receptor σ1/2 (IC50=47/56 nM), the 5-HT1A receptor (IC50=2.3 nM), and the 5-HT transporter (IC50=80 nM).

OPC-14523 hydrochloride

OPC-14523 hydrochloride

😃Good
TargetMol
Purity: 99.70%
Catalog No. T62711Alias VPI 013 hydrochlorideCas No. 145969-31-9
OPC-14523 hydrochloride is an orally active sigma and 5-HT1A receptor agonist with antidepressant-like activity, showing high affinity for the sigma receptor σ1/2 (IC50=47/56 nM), the 5-HT1A receptor (IC50=2.3 nM), and the 5-HT transporter (IC50=80 nM).
Pack SizePriceAvailabilityQuantity
5 mg$9706-8 weeks
10 mg$1,2896-8 weeks
25 mg$1,6196-8 weeks
50 mg$1,9806-8 weeks
100 mg$2,5006-8 weeks
1 mL x 10 mM (in DMSO)$1,0286-8 weeks
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Purity:99.70%
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Product Introduction

Bioactivity
Description
OPC-14523 hydrochloride is an orally active sigma and 5-HT1A receptor agonist with antidepressant-like activity, showing high affinity for the sigma receptor σ1/2 (IC50=47/56 nM), the 5-HT1A receptor (IC50=2.3 nM), and the 5-HT transporter (IC50=80 nM).
Targets&IC50
[3H]-5-HT:27 nM, 5-HT1A Receptor:2.3 nM, σ2:56 mM, σ1:47 nM
In vitro
OPC-14523 inhibits the in vitro reuptake of 3H-5-HT (IC50 = 27 nM), but exhibits very weak inhibition activity against the reuptake of 3H-NE and 3H-DA. OPC-14523 does not inhibit activity at the A or B receptors or muscarinic receptors.
In vivo
In Wistar rats (140-245 g), OPC-14523 hydrochloride (0.3-100 mg/kg; orally; daily for 0, 2, 4, 7 days) reduces immobility time in the depression experiment[1].
AliasVPI 013 hydrochloride
Chemical Properties
Molecular Weight450.4
FormulaC23H29Cl2N3O2
Cas No.145969-31-9
SmilesCl.COc1cccc2N(CCCN3CCN(CC3)c3cccc(Cl)c3)C(=O)CCc12
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 60 mg/mL (133.21 mM), Sonification is recommended.
H2O: 3 mg/mL (6.66 mM), Sonification is recommended.
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM2.2202 mL11.1012 mL22.2025 mL111.0124 mL
5 mM0.4440 mL2.2202 mL4.4405 mL22.2025 mL
DMSO
1mg5mg10mg50mg
10 mM0.2220 mL1.1101 mL2.2202 mL11.1012 mL
20 mM0.1110 mL0.5551 mL1.1101 mL5.5506 mL
50 mM0.0444 mL0.2220 mL0.4440 mL2.2202 mL
100 mM0.0222 mL0.1110 mL0.2220 mL1.1101 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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