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Apraclonidine hydrochloride

🥰Excellent
Catalog No. T21371Cas No. 73218-79-8
Alias P-aminoclonidine, Iopidine, Apraclonidinum, Apraclonidine HCl, Apraclonidina, ALO 2145, 4-Aminoclonidine

Apraclonidine hydrochloride (ALO 2145) is an α2-adrenergic agonist and a weak α-1 adrenergic receptor agonist. Apraclonidine hydrochloride lowers intraocular pressure in human eyes and can be used in studies about glaucoma therapy.

Apraclonidine hydrochloride

Apraclonidine hydrochloride

🥰Excellent
Purity: 98.01%
Catalog No. T21371Alias P-aminoclonidine, Iopidine, Apraclonidinum, Apraclonidine HCl, Apraclonidina, ALO 2145, 4-AminoclonidineCas No. 73218-79-8
Apraclonidine hydrochloride (ALO 2145) is an α2-adrenergic agonist and a weak α-1 adrenergic receptor agonist. Apraclonidine hydrochloride lowers intraocular pressure in human eyes and can be used in studies about glaucoma therapy.
Pack SizePriceAvailabilityQuantity
10 mg$44In Stock
25 mg$80In Stock
50 mg$118In Stock
100 mg$177In Stock
200 mg$248In Stock
1 mL x 10 mM (in DMSO)$30In Stock
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Purity:98.01%
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Product Introduction

Bioactivity
Description
Apraclonidine hydrochloride (ALO 2145) is an α2-adrenergic agonist and a weak α-1 adrenergic receptor agonist. Apraclonidine hydrochloride lowers intraocular pressure in human eyes and can be used in studies about glaucoma therapy.
In vitro
Apraclonidine hydrochloride penetrates the cornea and blood-brain barrier to a lesser extent[2].
In vivo
Apraclonidine hydrochloride elevats intraocular pressure as well as glaucoma. Apraclonidine reduces aqueous humor synthesis and vasoconstrictor actions at the anterior segment branches of the ophthalmic artery[2]. Apraclonidine (1.15%) causes a 98% inhibition of PGE2-induced aqueous flare elevationy[3].
AliasP-aminoclonidine, Iopidine, Apraclonidinum, Apraclonidine HCl, Apraclonidina, ALO 2145, 4-Aminoclonidine
Chemical Properties
Molecular Weight281.57
FormulaC9H11Cl3N4
Cas No.73218-79-8
SmilesCl.Nc1cc(Cl)c(NC2=NCCN2)c(Cl)c1
Relative Density.1.63 g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 112.5 mg/mL (399.5 mM), Sonication is recommended.
H2O: 11.2 mg/mL (40.0 mM)
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM3.5515 mL17.7576 mL35.5151 mL177.5757 mL
5 mM0.7103 mL3.5515 mL7.1030 mL35.5151 mL
10 mM0.3552 mL1.7758 mL3.5515 mL17.7576 mL
20 mM0.1776 mL0.8879 mL1.7758 mL8.8788 mL
DMSO
1mg5mg10mg50mg
50 mM0.0710 mL0.3552 mL0.7103 mL3.5515 mL
100 mM0.0355 mL0.1776 mL0.3552 mL1.7758 mL

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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
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