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Compound 48/80 trihydrochloride

Compound 48/80 trihydrochloride
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Compound 48/80 trihydrochloride

Catalog No. T13623Cas No. 848035-21-2
Compound 48/80 trihydrochloride (C48/80 trihydrochloride) is a mixture of N-methyl-p-methoxyphenethylamine and formaldehyde in a condensation reaction.Compound 48/80 trihydrochloride is a mast cell degranulator and histamine releaser. Compound 48/80 trihydrochloride inhibits phosphatidylinositol-specific phospholipase C activity in human platelets.
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Pack SizePriceAvailabilityQuantity
5 mg$49Backorder
1 mL x 10 mM (in DMSO)$98Backorder
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Product Introduction

Bioactivity
Description
Compound 48/80 trihydrochloride (C48/80 trihydrochloride) is a mixture of N-methyl-p-methoxyphenethylamine and formaldehyde in a condensation reaction.Compound 48/80 trihydrochloride is a mast cell degranulator and histamine releaser. Compound 48/80 trihydrochloride inhibits phosphatidylinositol-specific phospholipase C activity in human platelets.
In vitro
Compound 48/80 trihydrochloride inhibits both cytosolic and particulate phosphatidylinositol-specific phospholipase C activities with similar efficiency (IC50s: 2.1 μg/ml (supernatant) and 5.0 μg /ml (particulate fraction)). The aggregation of human platelets induced by ADP and PAF-acether is inhibited by Compound 48/80 [1].
In vivo
Compound 48/80 trihydrochloride causes oxidative stress in the rat adrenal gland through mast cell degranulation. Compound 48/80 trihydrochloride (0.75 mg/kg; i.p.; Killed after 0.5, 3, or 6 h) increases serum serotonin, histamine, and corticosterone levels at 0.5 h, but their increases were reduced thereafter [3].
AliasC48/80 trihydrochloride
Chemical Properties
Molecular Weight629.1
FormulaC32H48Cl3N3O3
Cas No.848035-21-2
Storage & Solubility Information
Storagestore at low temperature Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
H2O: 12.58 mg/mL (20 mM)
DMSO: 6.29 mg/mL (10 mM)
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM1.5896 mL7.9479 mL15.8957 mL79.4786 mL
5 mM0.3179 mL1.5896 mL3.1791 mL15.8957 mL
H2O
1mg5mg10mg50mg
10 mM0.1590 mL0.7948 mL1.5896 mL7.9479 mL
20 mM0.0795 mL0.3974 mL0.7948 mL3.9739 mL
50 mM0.0318 mL0.1590 mL0.3179 mL1.5896 mL
100 mM0.0159 mL0.0795 mL0.1590 mL0.7948 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
1 Enter information below:
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