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Dopropidil
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Catalog No. T11080Cas No. 79700-61-1
Dopropidil is a new anti-angina pectoris calcium regulator, which has intracellular calcium antagonist activity and anti-ischemic effects in various predicted animal models.
Dopropidil
😃Good
Catalog No. T11080Cas No. 79700-61-1
Dopropidil is a new anti-angina pectoris calcium regulator, which has intracellular calcium antagonist activity and anti-ischemic effects in various predicted animal models.
| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 25 mg | $1,520 | 6-8 weeks | |
| 50 mg | $1,980 | 6-8 weeks | |
| 100 mg | $2,500 | 6-8 weeks |
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Product Introduction
Bioactivity
Chemical Properties
| Description | Dopropidil is a new anti-angina pectoris calcium regulator, which has intracellular calcium antagonist activity and anti-ischemic effects in various predicted animal models. |
| In vitro | In the calcium-free medium (IC50 = 30.0 uM), dopredil can inhibit caffeine-induced contraction of rabbit renal arteries. Dopredil inhibits norepinephrine (NE)-induced responses with IC50 of 2.7 and 29.8 uM, respectively. At 3 μM and 10 μM, dopredil significantly reduced the maximum increase in diastolic pressure caused by veratrine (IC50 = 2.8 μM). |
| In vivo | Dopamine (1 and 2.5 mg/kg) dose-dependently reduced electrical (ST segment elevation), biochemical (lactate production and potassium release) and mechanical (myocardial segment contractility loss) disturbances caused by ischemia in anesthetized dogs. Intraduodenal administration of dopredil (50 mg/kg) can significantly reduce tachycardia caused by isoproterenol. This effect is evident between 15 and 120 minutes after application of the compound, indicating rapid absorption and long duration of action. In awake dogs, doprodil (12-14 mg/kg p.o.) can reduce the resting heart rate by about 10 beats/minute. |
| Molecular Weight | 321.5 |
| Formula | C20H35NO2 |
| Cas No. | 79700-61-1 |
| Relative Density. | 0.99g/cm3 |
Storage & Solubility Information
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
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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:
For example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . A total of 10 animals were administered, and the formula you used is 5% 
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 DMSO (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.
(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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