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Espindolol

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Catalog No. T27285Cas No. 26328-11-0
Alias MT-102, MT102, MT 102, AGI-001, AGI001, AGI 001

Espindolol is a novel non-selective β blocker with central 5-HT1a and partial β2 receptor agonist effects.

Espindolol

Espindolol

😃Good
Purity: 99.96%
Catalog No. T27285Alias MT-102, MT102, MT 102, AGI-001, AGI001, AGI 001Cas No. 26328-11-0
Espindolol is a novel non-selective β blocker with central 5-HT1a and partial β2 receptor agonist effects.
Pack SizePriceAvailabilityQuantity
1 mg$636-8 weeks
5 mg$1496-8 weeks
10 mg$1976-8 weeks
25 mg$3526-8 weeks
50 mg$5296-8 weeks
100 mg$7976-8 weeks
1 mL x 10 mM (in DMSO)$1646-8 weeks
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This molecule is a custom-made product. TargetMol has an excellent synthesis team with the experience and capability to provide you with cost-effective products. However, due to objective factors, there is a small probability that the synthesis may not be successful during the R&D process. We appreciate your understanding. If you have any questions, please feel free to contact us. We are committed to serving you wholeheartedly.
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Purity:99.96%
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Product Introduction

Bioactivity
Description
Espindolol is a novel non-selective β blocker with central 5-HT1a and partial β2 receptor agonist effects.
In vivo
Placebo-treated rats progressively lost body weight (-15.5 ± 7.2 g), lean mass (-1.5 ± 4.2 g), and fat mass (-15.6 ± 2.7 g), while espindolol treatment increased body weight (+8.0 ± 6.1 g, p < 0.05), particularly lean mass (+43.4 ± 3.5 g, p < 0.001), and reduced fat mass further (-38.6 ± 3.4 g, p < 0.001). Anabolic/catabolic signaling was assessed in gastrocnemius muscle. Espindolol decreased proteasome and caspase-3 proteolytic activities by approximately 50 % (all p < 0.05)[1].
AliasMT-102, MT102, MT 102, AGI-001, AGI001, AGI 001
Chemical Properties
Molecular Weight248.32
FormulaC14H20N2O2
Cas No.26328-11-0
SmilesCC(C)NC[C@H](O)COc1cccc2[nH]ccc12
Relative Density.1.152g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 55 mg/mL (221.49 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM4.0271 mL20.1353 mL40.2706 mL201.3531 mL
5 mM0.8054 mL4.0271 mL8.0541 mL40.2706 mL
10 mM0.4027 mL2.0135 mL4.0271 mL20.1353 mL
20 mM0.2014 mL1.0068 mL2.0135 mL10.0677 mL
50 mM0.0805 mL0.4027 mL0.8054 mL4.0271 mL
100 mM0.0403 mL0.2014 mL0.4027 mL2.0135 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% Saline/PBS/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 μLSaline/PBS/ddH2OTargetMol | 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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2 Enter the in vivo formulation:
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