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Dixyrazine

🥰Excellent
Catalog No. T19286Cas No. 2470-73-7
Alias UCB 3412

Dixyrazine (UCB 3412)has a transient antihypertensive effect, prevents cerebral edema induced by injections of ichthyosperm sulfate, and may be used in the study of neurologically related disorders.

Dixyrazine

Dixyrazine

🥰Excellent
Purity: 97.72%
Catalog No. T19286Alias UCB 3412Cas No. 2470-73-7
Dixyrazine (UCB 3412)has a transient antihypertensive effect, prevents cerebral edema induced by injections of ichthyosperm sulfate, and may be used in the study of neurologically related disorders.
Pack SizePriceAvailabilityQuantity
1 mg187 €In Stock
2 mg255 €In Stock
5 mg392 €In Stock
10 mg628 €In Stock
25 mg1.035 €In Stock
1 mL x 10 mM (in DMSO)368 €In Stock
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Purity:97.72%
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Product Introduction

Bioactivity
Description
Dixyrazine (UCB 3412)has a transient antihypertensive effect, prevents cerebral edema induced by injections of ichthyosperm sulfate, and may be used in the study of neurologically related disorders.
In vivo
Pretreatment with Dixyrazine (10 mg/kg) completely prevents brain edema and significantly reduces the increase of albumin in cerebrospinal fluid (CSF)[2]. In conscious rats subjected to acute hypertension provoked by i.v. adrenaline or bicuculline, the phenothiazine Dixyrazine (5 mg/kg i.v.) has minimal, transient hypotensive effects but significantly reduces the leakage of 126I labeled serum albumin. The diameters of pial arteries and veins are continuously measured with a multichannel videoangiometer through a closed cranial window in anesthetized rats before and after i.v. injection of Dixyrazine (5 mg/kg). Dixyrazine, at a dose of 5 mg/kg, induces a slight transitory decrease in blood pressure (10-20 mm Hg). The maximum mean arterial pressure (MAP) is slightly but not significantly lower in Dixyrazine-treated rats[1].
AliasUCB 3412
Chemical Properties
Molecular Weight427.6
FormulaC24H33N3O2S
Cas No.2470-73-7
SmilesCC(CN1CCN(CCOCCO)CC1)CN1c2ccccc2Sc2ccccc12
Relative Density.1.0745 g/cm3 (Estimated)
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 80 mg/mL (187.09 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.3386 mL11.6932 mL23.3863 mL116.9317 mL
5 mM0.4677 mL2.3386 mL4.6773 mL23.3863 mL
10 mM0.2339 mL1.1693 mL2.3386 mL11.6932 mL
20 mM0.1169 mL0.5847 mL1.1693 mL5.8466 mL
50 mM0.0468 mL0.2339 mL0.4677 mL2.3386 mL
100 mM0.0234 mL0.1169 mL0.2339 mL1.1693 mL

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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:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent 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 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
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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