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SMANT hydrochloride

🥰Excellent
Catalog No. T23370Cas No. 1177600-74-6
Alias SMANT HCl, N-(4-Bromophenyl)-3,5-dimethyl-1-piperidinepropanamide hydrochloride, N-(4-bromophenyl)-3-(3,5-dimethylpiperidin-1-yl)propanamide hydrochloride

SMANT hydrochloride (N-(4-bromophenyl)-3-(3,5-dimethylpiperidin-1-yl)propanamide hydrochloride) is an antagonist of Smoothened accumulation.

SMANT hydrochloride

SMANT hydrochloride

🥰Excellent
Purity: 100%
Catalog No. T23370Alias SMANT HCl, N-(4-Bromophenyl)-3,5-dimethyl-1-piperidinepropanamide hydrochloride, N-(4-bromophenyl)-3-(3,5-dimethylpiperidin-1-yl)propanamide hydrochlorideCas No. 1177600-74-6
SMANT hydrochloride (N-(4-bromophenyl)-3-(3,5-dimethylpiperidin-1-yl)propanamide hydrochloride) is an antagonist of Smoothened accumulation.
Pack SizePriceAvailabilityQuantity
5 mg$33In Stock
10 mg$53In Stock
25 mg$107In Stock
50 mg$188In Stock
100 mg$322In Stock
200 mg$465In Stock
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Purity:100%
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Product Introduction

Bioactivity
Description
SMANT hydrochloride (N-(4-bromophenyl)-3-(3,5-dimethylpiperidin-1-yl)propanamide hydrochloride) is an antagonist of Smoothened accumulation.
AliasSMANT HCl, N-(4-Bromophenyl)-3,5-dimethyl-1-piperidinepropanamide hydrochloride, N-(4-bromophenyl)-3-(3,5-dimethylpiperidin-1-yl)propanamide hydrochloride
Chemical Properties
Molecular Weight375.73
FormulaC16H24BrClN2O
Cas No.1177600-74-6
SmilesCN(C)CCN(Cc1ccccc1)C(=O)c1cc(-c2ccc(F)cc2)n2nc(cc2n1)C(C)(C)C
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: < 7.51 mg/mL
DMSO: 35 mg/mL (93.2 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.6615 mL13.3074 mL26.6149 mL133.0743 mL
5 mM0.5323 mL2.6615 mL5.3230 mL26.6149 mL
10 mM0.2661 mL1.3307 mL2.6615 mL13.3074 mL
20 mM0.1331 mL0.6654 mL1.3307 mL6.6537 mL
50 mM0.0532 mL0.2661 mL0.5323 mL2.6615 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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