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Camylofine

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Catalog No. T0346Cas No. 54-30-8
Alias Camylofin, Avacan, Adopon, Acamylophenine

Camylofine (Avacan) is an antimuscarinic, used for relaxing smooth muscle.

Camylofine

Camylofine

😃Good
Catalog No. T0346Alias Camylofin, Avacan, Adopon, AcamylophenineCas No. 54-30-8
Camylofine (Avacan) is an antimuscarinic, used for relaxing smooth muscle.
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Product Introduction

Bioactivity
Description
Camylofine (Avacan) is an antimuscarinic, used for relaxing smooth muscle.
AliasCamylofin, Avacan, Adopon, Acamylophenine
Chemical Properties
Molecular Weight393.4
FormulaC19H32N2O2·2HCl
Cas No.54-30-8
SmilesCCN(CC)CCNC(C(=O)OCCC(C)C)c1ccccc1
Relative Density.0.987g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 10 mM
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.5419 mL12.7097 mL25.4194 mL127.0971 mL
5 mM0.5084 mL2.5419 mL5.0839 mL25.4194 mL
10 mM0.2542 mL1.2710 mL2.5419 mL12.7097 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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