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ML 10302

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Catalog No. T60787Cas No. 148868-55-7

ML 10302 is a potent5-HT4 receptor agonist (Ki = 1.07 nM) that induces significant prokinesia both in the small bowel and colon by activating the cholinergic pathways. ML 10302 also shows the potential in neurology diseases research [1].

ML 10302
Other Forms of ML 10302:
ML 10302 hydrochlorideT22992186826-17-5
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ML 10302

😃Good
Catalog No. T60787Cas No. 148868-55-7
ML 10302 is a potent5-HT4 receptor agonist (Ki = 1.07 nM) that induces significant prokinesia both in the small bowel and colon by activating the cholinergic pathways. ML 10302 also shows the potential in neurology diseases research [1].
Pack SizePriceAvailabilityQuantity
25 mg$1,5201-2 weeks
50 mg$1,9801-2 weeks
100 mg$2,5001-2 weeks
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Product Introduction

Bioactivity
Description
ML 10302 is a potent5-HT4 receptor agonist (Ki = 1.07 nM) that induces significant prokinesia both in the small bowel and colon by activating the cholinergic pathways. ML 10302 also shows the potential in neurology diseases research [1].
Chemical Properties
Molecular Weight312.79
FormulaC15H21ClN2O3
Cas No.148868-55-7
Storage & Solubility Information
StorageShipping 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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