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LOC14

LOC14
LOC14 to be the most potent PDI inhibitor reported to date( EC50 : 500 nM)
Catalog No. T5534Cas No. 877963-94-5
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Purity:98.22%
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LOC14

Catalog No. T5534Cas No. 877963-94-5

LOC14 to be the most potent PDI inhibitor reported to date( EC50 : 500 nM)
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
Pack SizePriceAvailabilityQuantity
5 mg$43In Stock
10 mg$81In Stock
25 mg$171In Stock
50 mg$310In Stock
100 mg$543In Stock
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Product Introduction

Bioactivity
Description
LOC14 to be the most potent PDI inhibitor reported to date( EC50 : 500 nM)
Targets&IC50
PDI:500 nM(EC50)
In vitro
LOC14-induced oxidation of PDI has a neuroprotective effect not only in cell culture, but also in corticostriatal brain slice cultures[1].
In vivo
LOC14 showed high stability in liver microsomes and blood plasma, was tolerated at a high dose of 20 mg/kg in mice, and penetrated the BBB in vivo[1][2].
Animal Research
LOC14 levels were measured in mouse plasma, striatum and cerebral cortex using Ultra Performance Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS).?LOC14 was extracted from mouse plasma by mixing 100 μl of plasma with 900 μl of cold acetonitrile containing 25 ng/ml of cyclocreatine as an internal standard.?After mixing for 5 min. the sample was centrifuged for 10min and the organic layer was transferred to an LC-MS vial and dried under nitrogen.?The sample was reconstituted in 100 μl of 50% acetonitrile and 5 μl was injected onto the LC-MS.?Brain tissue samples were homogenized using a tissue tearor at a concentration of 150 mg/ml in cold LC-MS water followed by extraction with 1.8 ml of cold acetonitrile containing the cyclocreatine internal standard.?The brain samples were mixed and centrifuged and reconstituted the same as for the plasma samples[2].
Chemical Properties
Molecular Weight317.41
FormulaC16H19N3O2S
Cas No.877963-94-5
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 25 mg/mL (78.76 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.1505 mL15.7525 mL31.5050 mL157.5250 mL
5 mM0.6301 mL3.1505 mL6.3010 mL31.5050 mL
10 mM0.3150 mL1.5752 mL3.1505 mL15.7525 mL
20 mM0.1575 mL0.7876 mL1.5752 mL7.8762 mL
50 mM0.0630 mL0.3150 mL0.6301 mL3.1505 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:
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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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Keywords

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