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SR59230A hydrochloride

Catalog No. T13016LCas No. 1135278-41-9
Alias SR59230A HCl

SR59230A hydrochloride (SR59230A HCl) is a blood-brain permeable, selective and highly potent β3-adrenergic receptor antagonist that inhibits ultradian brown adipose tissue thermogenesis and interrupts associated paroxysmal brain and body heating.

SR59230A hydrochloride

SR59230A hydrochloride

Catalog No. T13016LAlias SR59230A HClCas No. 1135278-41-9
SR59230A hydrochloride (SR59230A HCl) is a blood-brain permeable, selective and highly potent β3-adrenergic receptor antagonist that inhibits ultradian brown adipose tissue thermogenesis and interrupts associated paroxysmal brain and body heating.
Pack SizePriceAvailabilityQuantity
1 mg$38In Stock
5 mg$82In Stock
10 mg$118In Stock
25 mg$193In Stock
50 mg$286In Stock
100 mg$423In Stock
1 mL x 10 mM (in DMSO)$98In Stock
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Product Introduction

Bioactivity
Description
SR59230A hydrochloride (SR59230A HCl) is a blood-brain permeable, selective and highly potent β3-adrenergic receptor antagonist that inhibits ultradian brown adipose tissue thermogenesis and interrupts associated paroxysmal brain and body heating.
Targets&IC50
β3-adrenoceptor:40 nM , β1-adrenoceptor:408 nM , β2-adrenoceptor:648 nM
In vitro
SR59230A hydrochloride (100 nM-50 μM; 24 hours) can reduce cell viability in a dose-dependent manner in Neuro-2A, BE(2)C and SK-N-BE(2) NB cell lines. [1]
In vivo
MDMA (20 mg/kg) caused a slow rise in body temperature, reaching a maximum temperature increase of 1.8°C at 130 min post-injection. SR59230A hydrochloride (0.5 mg/kg) was able to slightly but significantly alleviate the slow rise in body temperature induced by MDMA. SR59230A hydrochloride (5 mg/kg) exhibited a significant and pronounced early hypothermic response to MDMA. [2]
AliasSR59230A HCl
Chemical Properties
Molecular Weight361.91
FormulaC21H28ClNO2
Cas No.1135278-41-9
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 200 mg/mL(552.62 mM), Sonication is recommended.
H2O: 1 mg/mL(2.76 mM), Sonication is recommended.
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM2.7631 mL13.8156 mL27.6312 mL138.1559 mL
DMSO
1mg5mg10mg50mg
5 mM0.5526 mL2.7631 mL5.5262 mL27.6312 mL
10 mM0.2763 mL1.3816 mL2.7631 mL13.8156 mL
20 mM0.1382 mL0.6908 mL1.3816 mL6.9078 mL
50 mM0.0553 mL0.2763 mL0.5526 mL2.7631 mL
100 mM0.0276 mL0.1382 mL0.2763 mL1.3816 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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