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M8-B Hydrochloride

🥰Excellent
Catalog No. T8442Cas No. 883976-12-3

M8-B Hydrochloride is a selective transient receptor potential melastatin-8 (TRPM8) channel antagonist.

M8-B Hydrochloride

M8-B Hydrochloride

🥰Excellent
Purity: 99.33%
Catalog No. T8442Cas No. 883976-12-3
M8-B Hydrochloride is a selective transient receptor potential melastatin-8 (TRPM8) channel antagonist.
Pack SizePriceAvailabilityQuantity
2 mg$30In Stock
5 mg$48In Stock
10 mg$68In Stock
25 mg$148In Stock
50 mg$238In Stock
100 mg$353In Stock
200 mg$493In Stock
1 mL x 10 mM (in DMSO)$58In Stock
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Purity:99.33%
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Product Introduction

Bioactivity
Description
M8-B Hydrochloride is a selective transient receptor potential melastatin-8 (TRPM8) channel antagonist.
In vivo
M8 B, a TRPM8 antagonist, can reduce body temperature.M8 B decreased the body temperature of rat pups and increased the latency to the first febrile seizure, implying a significant protective effect.?It also induced a significant anticonvulsant effect in PTZ but not electroshock induced convulsions.?M8 B showed anticonvulsant effects in both febrile and PTZ induced seizures.?M8 B had a hypothermic effect with significant protective effects on febrile and PTZ induced seizures.
Animal Research
Eight day old male Wistar rat pups were used for induction of febrile seizure.?M8 B and diazepam were injected intraperitoneally.?The rat pups were then transferred to a heated plexiglas chamber and the latency to the first febrile seizure was measured.?In addition, different groups of mice were pretreated with M8 B and received a convulsant dose of pentylenetetrazol (PTZ).?Latencies to stages 2 and 4 and duration of stage 5 seizure episodes were measured.The effect of M8 B on electroshock induced seizures was also investigated and hindlimb extension time was measured[1].
Chemical Properties
Molecular Weight432.96
FormulaC22H25ClN2O3S
Cas No.883976-12-3
SmilesCl.COc1cc(CN(CCN)C(=O)c2cccs2)ccc1OCc1ccccc1
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
DMSO: 27.5 mg/mL (63.52 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.3097 mL11.5484 mL23.0968 mL115.4841 mL
5 mM0.4619 mL2.3097 mL4.6194 mL23.0968 mL
10 mM0.2310 mL1.1548 mL2.3097 mL11.5484 mL
20 mM0.1155 mL0.5774 mL1.1548 mL5.7742 mL
50 mM0.0462 mL0.2310 mL0.4619 mL2.3097 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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