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BAN ORL 24 dihydrochloride

Catalog No. T10457Cas No. 1401463-54-4

BAN ORL 24 is a highly potent nociceptin/orphan FQ (N/OFQ) receptor (NOP) antagonist that can be used to study neurological diseases.

BAN ORL 24 dihydrochloride

BAN ORL 24 dihydrochloride

Purity: 95.03%
Catalog No. T10457Cas No. 1401463-54-4
BAN ORL 24 is a highly potent nociceptin/orphan FQ (N/OFQ) receptor (NOP) antagonist that can be used to study neurological diseases.
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2 mg$74In Stock
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Purity:95.03%
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Product Introduction

Bioactivity
Description
BAN ORL 24 is a highly potent nociceptin/orphan FQ (N/OFQ) receptor (NOP) antagonist that can be used to study neurological diseases.
Targets&IC50
NOP receptor:50 μM, μ opioid receptor:0.224 μM
In vitro
BAN ORL 24 has antagonist for NOR (IC50=50 μM) and MOR (opioid receptor subtype) (IC50=0.224 μM). [1]
In vivo
BAN ORL 24 (10 mg/kg; i.v.) attenuated the duration of the thermal nociceptive antisensitization effect of BPRIM97 and inhibited BPRIM97-induced antinociceptive sensitization at 90 min postinjection. In tail-clip testing, BAN ORL 24 did not attenuate BPR1M97-induced antinociceptive sensitization at 30 min postinjection. [2]
Chemical Properties
Molecular Weight506.51
FormulaC27H37Cl2N3O2
Cas No.1401463-54-4
Storage & Solubility Information
Storagekeep away from direct sunlight,store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: 80 mg/mL (157.94 mM.), Sonication is recommended.
DMSO: 180 mg/mL, (355.37 mM.), Sonication is recommended.
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM1.9743 mL9.8715 mL19.7429 mL98.7147 mL
5 mM0.3949 mL1.9743 mL3.9486 mL19.7429 mL
10 mM0.1974 mL0.9871 mL1.9743 mL9.8715 mL
20 mM0.0987 mL0.4936 mL0.9871 mL4.9357 mL
50 mM0.0395 mL0.1974 mL0.3949 mL1.9743 mL
100 mM0.0197 mL0.0987 mL0.1974 mL0.9871 mL

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In Vivo Formulation Calculator (Clear solution)

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.
1 Enter information below:
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2 Enter the in vivo formulation:
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Dose Conversion

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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

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