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Rocastine

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Catalog No. T16778Cas No. 91833-49-7
Alias AHR-11325

Rocastine (AHR-11325) is a selective and potent non-sedating H1 receptor antagonist.

Rocastine

Rocastine

😃Good
Purity: 98.26%
Catalog No. T16778Alias AHR-11325Cas No. 91833-49-7
Rocastine (AHR-11325) is a selective and potent non-sedating H1 receptor antagonist.
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1 mg$7006-8 weeks
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Purity:98.26%
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Product Introduction

Bioactivity
Description
Rocastine (AHR-11325) is a selective and potent non-sedating H1 receptor antagonist.
In vivo
Rocastine is effective with a 15-minute pretreatment time (PD50 = 0.13 mg/kg) as it is with a 1-hour pretreatment time (PD50 = 0.12 mg/kg). In protecting guinea pigs from collapse induced by aerosolized antigen, rocastine demonstrates approximately 36 times more potency than diphenhydramine and is as potent as oxatomide and terfenadine. At doses in vast excess (150 times) of its antihistaminic dose, rocastine does not alter the EEG of cats, nor does it potentiate yohimbine toxicity in mice[1].
AliasAHR-11325
Chemical Properties
Molecular Weight265.37
FormulaC13H19N3OS
Cas No.91833-49-7
SmilesS=C1C2=CC=CN=C2OC(CN1C)CCN(C)C
Relative Density.1.20 g/cm3 (Predicted)
Storage & Solubility Information
Storagestore at low temperature | 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:
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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