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AF-710B

TargetMol
Catalog No. T23649Cas No. 1235733-73-9
Alias ANAVEX 3-71, AF710B, AF 710B

AF-710B is a specific variant of M1 muscarinic and Sigma-1 receptor agonist used in the study of neurological disorders such as Alzheimer's disease dementia and schizophrenia.

AF-710B

AF-710B

TargetMol
Purity: 99.89%
Catalog No. T23649Alias ANAVEX 3-71, AF710B, AF 710BCas No. 1235733-73-9
AF-710B is a specific variant of M1 muscarinic and Sigma-1 receptor agonist used in the study of neurological disorders such as Alzheimer's disease dementia and schizophrenia.
Pack SizePriceAvailabilityQuantity
1 mg$333In Stock
2 mg$495In Stock
5 mg$790In Stock
10 mg$1,120In Stock
25 mg$1,670In Stock
50 mg$2,180In Stock
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Purity:99.89%
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Product Introduction

Bioactivity
Description
AF-710B is a specific variant of M1 muscarinic and Sigma-1 receptor agonist used in the study of neurological disorders such as Alzheimer's disease dementia and schizophrenia.
AliasANAVEX 3-71, AF710B, AF 710B
Chemical Properties
Molecular Weight357.51
FormulaC20H27N3OS
Cas No.1235733-73-9
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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