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Midaglizole hydrochloride

Midaglizole hydrochloride
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Purity:100%
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Midaglizole hydrochloride

Catalog No. T11015Cas No. 79689-25-1
Midaglizole hydrochloride ((±)-DG5128) (DG5128) is a preferred α2-adrenoceptor antagonist. Midazolazole hydrochloride (DG5128) has an affinity for α2-adrenoceptor (pKi = 6.28) 7.4 times higher than that of α1-adrenoceptor.
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Pack SizePriceAvailabilityQuantity
1 mg$87In Stock
5 mg$213In Stock
10 mg$349In Stock
25 mg$569In Stock
50 mg$774In Stock
100 mg$987In Stock
500 mg$1,980In Stock
1 mL x 10 mM (in DMSO)$271In Stock
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Product Introduction

Bioactivity
Description
Midaglizole hydrochloride ((±)-DG5128) (DG5128) is a preferred α2-adrenoceptor antagonist. Midazolazole hydrochloride (DG5128) has an affinity for α2-adrenoceptor (pKi = 6.28) 7.4 times higher than that of α1-adrenoceptor.
In vitro
The inhibitory effect of midazolam (DG-5128) at a concentration of up to 10 μM in the cerebral cerebral membrane of [3H] clonidine is more effective than that of [3H] prazosin. The suppression method is uniform and conforms to the simple law of mass action. The EC50 values of midazolazole-induced insulin release in rat pancreatic islets and MIN6β cell lines were 200 nM and 24 μM, respectively. The IC50 values of midazolam for Kir6.2 and Kir6.2/SUR1 induced KATP current were 3.8 μM and 4.4 uM, respectively.
In vivo
Midaglizole (3 and 30 mg/kg, i.v.) increases blood pressure in pithed rats[1].
Alias(±)-DG5128, (±)-DG5128 hydrochloride, DG5128 hydrochloride, DG5128
Chemical Properties
Molecular Weight324.25
FormulaC16H19Cl2N3
Cas No.79689-25-1
Storage & Solubility Information
Storage Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
DMSO: 45 mg/mL (138.78 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.0840 mL15.4202 mL30.8404 mL154.2020 mL
5 mM0.6168 mL3.0840 mL6.1681 mL30.8404 mL
10 mM0.3084 mL1.5420 mL3.0840 mL15.4202 mL
20 mM0.1542 mL0.7710 mL1.5420 mL7.7101 mL
50 mM0.0617 mL0.3084 mL0.6168 mL3.0840 mL
100 mM0.0308 mL0.1542 mL0.3084 mL1.5420 mL

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