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Cinanserin hydrochloride

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Catalog No. T14968Cas No. 54-84-2
Alias SQ 10643

Cinanserin hydrochloride (SQ 10643), a high-affinity antagonist of the 5-HT2 receptor (Ki: 41 nM), is also a 3C-like protease inhibitor of severe acute respiratory syndrome coronavirus.

Cinanserin hydrochloride

Cinanserin hydrochloride

🥰Excellent
Purity: 99.32%
Catalog No. T14968Alias SQ 10643Cas No. 54-84-2
Cinanserin hydrochloride (SQ 10643), a high-affinity antagonist of the 5-HT2 receptor (Ki: 41 nM), is also a 3C-like protease inhibitor of severe acute respiratory syndrome coronavirus.
Pack SizePriceAvailabilityQuantity
1 mg$30In Stock
5 mg$68In Stock
10 mg$109In Stock
25 mg$218In Stock
50 mg$397In Stock
100 mg$597In Stock
1 mL x 10 mM (in DMSO)$119In Stock
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Purity:99.32%
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Product Introduction

Bioactivity
Description
Cinanserin hydrochloride (SQ 10643), a high-affinity antagonist of the 5-HT2 receptor (Ki: 41 nM), is also a 3C-like protease inhibitor of severe acute respiratory syndrome coronavirus.
Targets&IC50
3CLpro:, 5-HT2 receptor:41 nM (ki)
In vitro
Cinanserin and Cinanserin hydrochloride inhibit the catalytic activity of SARS-CoV 3CLpro and HCoV-229E 3CLpro (IC50: 4.68 μM and 5.68 μM). Cinanserin/Cinanserin hydrochloride has a binding affinity to SARS-CoV 3CLpro, HCoV-229E 3CLpro, with the KD values of 49.4 μM/78.0 μM for SARS-associated coronavirus (SARS-CoV) 3CLpro[1].
In vivo
Cinanserin (5 mg/kg; intravenous injection; 2 hours; male Wistar rats) treatment significantly reduces systemic burn edema to shamburn levels[2].
AliasSQ 10643
Chemical Properties
Molecular Weight376.94
FormulaC20H25ClN2OS
Cas No.54-84-2
SmilesCl.CN(C)CCCSc1ccccc1NC(=O)C=Cc1ccccc1
Relative Density.1.22 g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 125 mg/mL (331.62 mM), Sonication is recommended.
H2O: 100 mg/mL (265.29 mM), Sonication is recommended.
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM2.6529 mL13.2647 mL26.5294 mL132.6471 mL
5 mM0.5306 mL2.6529 mL5.3059 mL26.5294 mL
10 mM0.2653 mL1.3265 mL2.6529 mL13.2647 mL
20 mM0.1326 mL0.6632 mL1.3265 mL6.6324 mL
50 mM0.0531 mL0.2653 mL0.5306 mL2.6529 mL
100 mM0.0265 mL0.1326 mL0.2653 mL1.3265 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
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