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Midaglizole hydrochloride
🥰Excellent
Catalog No. T11015Cas No. 79689-25-1
Alias DG5128 hydrochloride, (±)-DG5128 hydrochloride
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.
Midaglizole hydrochloride
🥰Excellent
Purity: 100%
Catalog No. T11015Alias DG5128 hydrochloride, (±)-DG5128 hydrochlorideCas 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.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | 49 € | In Stock | |
| 5 mg | 121 € | In Stock | |
| 10 mg | 198 € | In Stock | |
| 25 mg | 323 € | In Stock | |
| 50 mg | 439 € | In Stock | |
| 100 mg | 562 € | In Stock | |
| 200 mg | 743 € | In Stock | |
| 1 mL x 10 mM (in DMSO) | 154 € | In Stock |
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Purity:100%
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All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.Product Introduction
Bioactivity
Chemical Properties
| 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. |
| Targets&IC50 | α2-adrenoceptor:6.28(pKi ) |
| 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.) elevates blood pressure in pithed rats[1]. |
| Alias | DG5128 hydrochloride, (±)-DG5128 hydrochloride |
| Molecular Weight | 324.25 |
| Formula | C16H19Cl2N3 |
| Cas No. | 79689-25-1 |
| Smiles | C1(C(CC2=NCCN2)C3=CC=CC=C3)=NC=CC=C1.Cl.Cl |
| Relative Density. | 1.31g/cm3 |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 45 mg/mL (138.78 mM), Sonication and heating to 60℃ are recommended.  | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
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(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 DMSO main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarify
main solution, add 300 μLPEG300 mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2O mix well and clarifyFor Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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