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JNJ-10311795

🥰Excellent
Catalog No. T27660Cas No. 518062-14-1
Alias RWJ-355871, RWJ355871, JNJ10311795

JNJ-10311795 (RWJ-355871) is a potent dual inhibitor of neutrophil elastase (Ki = 38 nM) and mast cell chymase (Ki = 2.3 nM) with significant anti-inflammatory activity, useful for studying pneumonia.

JNJ-10311795

JNJ-10311795

🥰Excellent
Purity: 97.43%
Catalog No. T27660Alias RWJ-355871, RWJ355871, JNJ10311795Cas No. 518062-14-1
JNJ-10311795 (RWJ-355871) is a potent dual inhibitor of neutrophil elastase (Ki = 38 nM) and mast cell chymase (Ki = 2.3 nM) with significant anti-inflammatory activity, useful for studying pneumonia.
Pack SizePriceAvailabilityQuantity
1 mg$293In Stock
5 mg$722In Stock
10 mg$987In Stock
25 mg$1,520In Stock
50 mg$1,980In Stock
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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:97.43%
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Product Introduction

Bioactivity
Description
JNJ-10311795 (RWJ-355871) is a potent dual inhibitor of neutrophil elastase (Ki = 38 nM) and mast cell chymase (Ki = 2.3 nM) with significant anti-inflammatory activity, useful for studying pneumonia.
Targets&IC50
Cathepsin G:82 nM
In vitro
JNJ-10311795 is a novel effective dual inhibitor of neutrophil cathepsin G (K (i) = 38 nM, IC50 = 82 nM) and mast cell rennet (K (i) = 2.3 nM). [1]
In vivo
In a rat model of inflammation, JNJ-10311795 (0.5 mg/kg intravenously) was administered 30 minutes before glycogen therapy, followed by 10 mg/kg/h intravenous infusion for 4.5 hours (total dose = 45.5 mg/kg). The increase in myeloperoxidase was reduced by 50% (neutrophil counts were reduced by 50%). [1]
AliasRWJ-355871, RWJ355871, JNJ10311795
Chemical Properties
Molecular Weight670.69
FormulaC40H35N2O6P
Cas No.518062-14-1
SmilesO=C(C=1C=CC=2C=CC=CC2C1)N3CCC(N(C(=O)C4=CC=5C=CC=CC5C=C4C(=O)C(C6=CC=CC=7C=CC=CC76)P(=O)(O)O)C)CC3
Relative Density.1.41 g/cm3 (Predicted)
Storage & Solubility Information
Storagekeep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

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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
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