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Lofexidine

Lofexidine
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Purity:99.08%
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Lofexidine

Catalog No. T7160Cas No. 31036-80-3
Lofexidine is a selective α2-receptor agonist, Lofexidine reduces narcotic withdrawal symptoms.
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Pack SizePriceAvailabilityQuantity
5 mg$30In Stock
50 mg$85In Stock
1 mL x 10 mM (in DMSO)$30In Stock
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Related Compound Libraries of "Lofexidine"

Product Introduction

Bioactivity
Description
Lofexidine is a selective α2-receptor agonist, Lofexidine reduces narcotic withdrawal symptoms.
In vivo
Lofexidine significantly decreased SOWS scores compared to placebo and demonstrated better retention rates in participants undergoing opioid withdrawal. Lofexidine potentially offers a useful non-opioid alternative to treat opioid withdrawal symptoms[1].
Animal Research
8-day, randomized, double-blind, placebo-controlled, parallel-group study in 264 patients dependent on short-acting opioids evaluated the efficacy of lofexidine hydrochloride in reducing withdrawal symptoms in patients undergoing opioid withdrawal.?The primary efficacy measures were SOWS-Gossop on Day 3 and time-to-dropout.?Secondary endpoints included the proportion of participants who were completers;?area under the 5-day SOWS-Gossop - time curve (i.e., AUC1-5), and daily mean SOWS-Gossop, OOWS-Handelsman, MCGI (subject and rater), and VAS-E scores.?Participants received lofexidine HCl 3.2mg daily in four divided doses or matching placebo on Days 1-5, followed by 2days of placebo[1].
Chemical Properties
Molecular Weight259.13
FormulaC11H12Cl2N2O
Cas No.31036-80-3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
DMSO: 62.5 mg/mL (241.19 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.8591 mL19.2953 mL38.5907 mL192.9533 mL
5 mM0.7718 mL3.8591 mL7.7181 mL38.5907 mL
10 mM0.3859 mL1.9295 mL3.8591 mL19.2953 mL
20 mM0.1930 mL0.9648 mL1.9295 mL9.6477 mL
50 mM0.0772 mL0.3859 mL0.7718 mL3.8591 mL
100 mM0.0386 mL0.1930 mL0.3859 mL1.9295 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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