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Fenclonine

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Catalog No. T1447Cas No. 7424-00-2
Alias PCPA, Fenchlonine, DL-4-Chlorophenylalanine, CP-10188, 4-Chloro-DL-phenylalanine

Fenclonine (CP-10188) is a selective and irreversible inhibitor of tryptophan hydroxylase, a rate-limiting enzyme in the biosynthesis of serotonin (5-HYDROXYTRYPTAMINE). Fenclonine(CP-10188) acts pharmacologically to deplete endogenous levels of serotonin.

Fenclonine

Fenclonine

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Purity: 99.96%
Catalog No. T1447Alias PCPA, Fenchlonine, DL-4-Chlorophenylalanine, CP-10188, 4-Chloro-DL-phenylalanineCas No. 7424-00-2
Fenclonine (CP-10188) is a selective and irreversible inhibitor of tryptophan hydroxylase, a rate-limiting enzyme in the biosynthesis of serotonin (5-HYDROXYTRYPTAMINE). Fenclonine(CP-10188) acts pharmacologically to deplete endogenous levels of serotonin.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
200 mg$30In StockIn Stock
500 mg$42-In Stock
1 g$53-In Stock
5 g$126-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.96%
Color:White
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Product Introduction

Fenclonine AI Summary
Fenclonine exhibits a broad range of bioactivities across various biological assays. It notably inhibits multiple enzymes such as Endonuclease IV, Bloom's syndrome helicase (BLM), Histone Lysine Methyltransferase G9a, Mammalian Selenoprotein Thioredoxin Reductase 1 (TrxR1), and Human Flap endonuclease 1 (FEN1). Additionally, it affects the human hERG channel activity, modulates Human Peripheral Myelin Protein 22 expression/activity, and enhances Arylsulfatase A (ASA1). It also interacts with HP1-beta Chromodomain and shows antiviral properties by inhibiting binding or entry of Marburg Virus and blocking Ebola Virus entry. Potencies in these assays range from 4.0 nM to 100000.0 nM. Fenclonine demonstrates notable antiviral activity against SARS-CoV-2, as evidenced by inhibiting SARS-CoV-2 induced cytotoxicity in both Caco-2 and VERO-6 cells at a concentration of 10 µM after 48 hours, showing inhibition rates of -0.58% and 0.09% respectively. Additionally, it exhibits a SARS-CoV-2 3CL-Pro protease inhibition percentage of 0.8074% at 20 µM, and an IC50 value for this antiviral activity is greater than 20000.0 nM. Furthermore, Fenclonine demonstrates inhibitory activity on human HDAC6 enzyme, showing 19.51% inhibition with a commercial peptide substrate and 6.14% with a custom peptide substrate in enzymatic assays..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Fenclonine (CP-10188) is a selective and irreversible inhibitor of tryptophan hydroxylase, a rate-limiting enzyme in the biosynthesis of serotonin (5-HYDROXYTRYPTAMINE). Fenclonine(CP-10188) acts pharmacologically to deplete endogenous levels of serotonin.
SynonymsPCPA, Fenchlonine, DL-4-Chlorophenylalanine, CP-10188, 4-Chloro-DL-phenylalanine
Chemical Properties
Molecular Weight199.63
FormulaC9H10ClNO2
Cas No.7424-00-2
SmilesNC(Cc1ccc(Cl)cc1)C(O)=O
Relative Density.1.336 g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
H2O: 1 mg/mL (5.01 mM), Sonication is recommended.
DMSO: 33 mg/mL (165.31 mM), pH is adjusted to 3 with HCl. Sonication is recommended.
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM5.0093 mL25.0463 mL50.0927 mL250.4634 mL
5 mM1.0019 mL5.0093 mL10.0185 mL50.0927 mL
DMSO
1mg5mg10mg50mg
10 mM0.5009 mL2.5046 mL5.0093 mL25.0463 mL
20 mM0.2505 mL1.2523 mL2.5046 mL12.5232 mL
50 mM0.1002 mL0.5009 mL1.0019 mL5.0093 mL
100 mM0.0501 mL0.2505 mL0.5009 mL2.5046 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 stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
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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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