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Coptisine chloride

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Catalog No. T5S0056Cas No. 6020-18-4
Alias Q-100696, NSC-119754

1. Coptisine chloride (NSC-119754) can be absorbed across intestinal epithelial cells, and completely absorbed compounds.

Coptisine chloride

Coptisine chloride

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Purity: 99.93%
Catalog No. T5S0056Alias Q-100696, NSC-119754Cas No. 6020-18-4
1. Coptisine chloride (NSC-119754) can be absorbed across intestinal epithelial cells, and completely absorbed compounds.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
5 mg$59In StockIn Stock
10 mg$95In StockIn Stock
25 mg$197In StockIn Stock
50 mg$293In StockIn Stock
100 mg$437In StockIn Stock
500 mg$982-In Stock
1 mL x 10 mM (in DMSO)$66In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.93%
Appearance:Solid
Color:White to Red
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Product Introduction

Coptisine chloride AI Summary
Coptisine chloride exhibits bioactivity as an inhibitor of HIV1 RT with an IC50 value of less than 150.0 μg/mL. It demonstrates cytotoxic activity against human A549 and HCT15 cells with IC50 values of 23,960.0 nM and 29,070.0 nM, respectively, but not significantly against SKOV3 and SK-MEL-2 cells as their IC50 values are greater than 30,000.0 nM. Additionally, Coptisine chloride shows antiproliferative activity across various cell types, including rat and human cells, with GI50 values ranging from 3,300.0 nM to 104,940.0 nM. The compound upregulates Rgc32 and Gadd45a mRNA in rat A10 cells and Gadd45a mRNA in rat 3Y1 cells at 30 μM. Notably, it also demonstrates significant growth inhibition in a range of human tumor cell lines, including breast, renal, lung, leukemia, melanoma, ovarian, prostate, and central nervous system cells, with GI50 values spanning from 192.3 nM to 12,502.59 nM. The compound shows varying degrees of cytotoxicity against human Bel7402, A549, HCT8, and C33A cell lines, with specific growth inhibition rates and IC50 values. For rat IEC-6 cells, Coptisine chloride results in a 79.0% survival rate at 10 μM concentration and activates XBP1 transcriptional activity with a ratio of 0.78 compared to control after 48 hours..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
1. Coptisine chloride (NSC-119754) can be absorbed across intestinal epithelial cells, and completely absorbed compounds.
Targets&IC50
IDO:6.3 μM.
SynonymsQ-100696, NSC-119754
Chemical Properties
Molecular Weight355.77
FormulaC19H14ClNO4
Cas No.6020-18-4
Smiles[Cl-].C1Oc2cc3CC[n+]4cc5c6OCOc6ccc5cc4-c3cc2O1
Relative Density.1.51g/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
DMSO: 5.56 mg/mL (15.63 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.8108 mL14.0540 mL28.1080 mL140.5402 mL
5 mM0.5622 mL2.8108 mL5.6216 mL28.1080 mL
10 mM0.2811 mL1.4054 mL2.8108 mL14.0540 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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%
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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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