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SDZ-NVI-085

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Catalog No. T28741Cas No. 104195-17-7
Alias SDZ NVI 085, naphtoxazine

SDZ-NVI-085 is an α1 adrenergic receptor agonist and a competitive antagonist of 5-hydroxytryptamine.

SDZ-NVI-085

SDZ-NVI-085

😃Good
Catalog No. T28741Alias SDZ NVI 085, naphtoxazineCas No. 104195-17-7
SDZ-NVI-085 is an α1 adrenergic receptor agonist and a competitive antagonist of 5-hydroxytryptamine.
Pack SizePriceAvailabilityQuantity
25 mg$1,970 8-10 weeks
50 mg$2,580 8-10 weeks
100 mg$3,400 8-10 weeks
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Product Introduction

Bioactivity
Description
SDZ-NVI-085 is an α1 adrenergic receptor agonist and a competitive antagonist of 5-hydroxytryptamine.
AliasSDZ NVI 085, naphtoxazine
Chemical Properties
Molecular Weight279.4
FormulaC15H21NO2S
Cas No.104195-17-7
Relative Density.1.19g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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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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Keywords

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