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DF-1111301

TargetMol
DF-1111301
DF-1111301 is a novel anti-allergic compound with anti-histamine H1 and anti-PAF activity.
Catalog No. T27159Cas No. 160665-99-6
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Purity:99.63%
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DF-1111301

TargetMol
Catalog No. T27159Alias DF1111301, DF 1111301Cas No. 160665-99-6

DF-1111301 is a novel anti-allergic compound with anti-histamine H1 and anti-PAF activity.
With extensive experience in compound synthesis, we can provide rapid custom synthesis services for this product according to your research needs.
Pack SizePriceAvailabilityQuantity
1 mg$293In Stock
5 mg$722In Stock
10 mg$987In Stock
25 mg$1,520In Stock
50 mg$1,980In Stock
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Product Introduction

Bioactivity
Description
DF-1111301 is a novel anti-allergic compound with anti-histamine H1 and anti-PAF activity.
AliasDF1111301, DF 1111301
Chemical Properties
Molecular Weight334.29
FormulaC15H25Cl2N3O
Cas No.160665-99-6
Storage & Solubility Information
StoragePowder: -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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