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JHU37160

JHU37160
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Purity:99.25%
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JHU37160

Catalog No. T9018Cas No. 2369979-68-8
JHU37160 (JHU 37160) is a Designer Receptors Exclusively Activated by Designer Drug (DREADD) agonist with Ki of 1.9 nM and 3.6 nM for human muscarinic acetylcholine M3 receptors (hM3Dq) and hM4Di in vitro, respectively. And EC50 values are 18.5 nM and 0.2 nM for hM3Dq and hM4Di in fluorescent and BRET-based assays in HEK-293 cells, respectively.
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Pack SizePriceAvailabilityQuantity
10 mg$42In Stock
25 mg$78In Stock
50 mg$125In Stock
100 mg$197In Stock
1 mL x 10 mM (in DMSO)$32In Stock
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Product Introduction

Bioactivity
Description
JHU37160 (JHU 37160) is a Designer Receptors Exclusively Activated by Designer Drug (DREADD) agonist with Ki of 1.9 nM and 3.6 nM for human muscarinic acetylcholine M3 receptors (hM3Dq) and hM4Di in vitro, respectively. And EC50 values are 18.5 nM and 0.2 nM for hM3Dq and hM4Di in fluorescent and BRET-based assays in HEK-293 cells, respectively.
Targets&IC50
M4Di DREADD (human):0.2 nM (EC50), M3Dq DREADD (human):18.5 nM (EC50)
In vitro
JHU 37160 is a potent agonist of DREADD with high potency and efficacy in fluorescent and BRET-based assays in HEK-293 cells, whereas no responses are observed in untransfected HEK-293 cells
In vivo
JHU 37160 exhibits high in vivo DREADD potency. It exhibits selective [3H]clozapine displacement from DREADDs in brain tissue from WT and D1-DREADD mice
AliasJHU 37160
Chemical Properties
Molecular Weight358.84
FormulaC19H20ClFN4
Cas No.2369979-68-8
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
Ethanol: 72 mg/mL (200.65 mM)
DMSO: 72 mg/mL (200.65 mM)
Solution Preparation Table
Ethanol/DMSO
1mg5mg10mg50mg
1 mM2.7868 mL13.9338 mL27.8676 mL139.3379 mL
5 mM0.5574 mL2.7868 mL5.5735 mL27.8676 mL
10 mM0.2787 mL1.3934 mL2.7868 mL13.9338 mL
20 mM0.1393 mL0.6967 mL1.3934 mL6.9669 mL
50 mM0.0557 mL0.2787 mL0.5574 mL2.7868 mL
100 mM0.0279 mL0.1393 mL0.2787 mL1.3934 mL

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