Powder: -20°C for 3 years | In solvent: -80°C for 1 year
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.
説明 | 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]. |
別名 | Iopidine, ALO 2145, Apraclonidina, P-aminoclonidine, 4-Aminoclonidine, Apraclonidine HCl, Apraclonidinum |
分子量 | 281.57 |
分子式 | C9H11Cl3N4 |
CAS No. | 73218-79-8 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 112.5 mg/mL (399.5 mM), Sonication is recommended.
H2O: 11.2 mg/mL (40.0 mM)
You can also refer to dose conversion for different animals. 詳細
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Apraclonidine hydrochloride 73218-79-8 GPCR/G Protein Neuroscience Adrenergic Receptor Iopidine ALO 2145 ALO2145 Apraclonidine Hydrochloride Apraclonidina P-aminoclonidine 4-Aminoclonidine Apraclonidine HCl Apraclonidinum ALO-2145 Inhibitor inhibitor inhibit