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LOC14

🥰Excellent
Catalog No. T5534Cas No. 877963-94-5

LOC14 to be the most potent PDI inhibitor reported to date( EC50 : 500 nM)

LOC14

LOC14

🥰Excellent
Purity: 98.22%
Catalog No. T5534Cas No. 877963-94-5
LOC14 to be the most potent PDI inhibitor reported to date( EC50 : 500 nM)
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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Purity:98.22%
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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
SmilesO=C(C1CC1)N1CCN(Cn2sc3ccccc3c2=O)CC1
Relative Density.1.390 g/cm3 (Predicted)
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:
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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Keywords

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