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4-(4-Aminophenoxy)-N-methyl-2-pyridinecarboxamide

CAS# 284462-37-9

4-(4-Aminophenoxy)-N-methyl-2-pyridinecarboxamide

Catalog No. BCC8649----Order now to get a substantial discount!

Product Name & Size Price Stock
4-(4-Aminophenoxy)-N-methyl-2-pyridinecarboxamide:5mg Please Inquire In Stock
4-(4-Aminophenoxy)-N-methyl-2-pyridinecarboxamide:10mg Please Inquire In Stock
4-(4-Aminophenoxy)-N-methyl-2-pyridinecarboxamide:20mg Please Inquire In Stock
4-(4-Aminophenoxy)-N-methyl-2-pyridinecarboxamide:50mg Please Inquire In Stock

Quality Control of 4-(4-Aminophenoxy)-N-methyl-2-pyridinecarboxamide

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Chemical structure

4-(4-Aminophenoxy)-N-methyl-2-pyridinecarboxamide

3D structure

Chemical Properties of 4-(4-Aminophenoxy)-N-methyl-2-pyridinecarboxamide

Cas No. 284462-37-9 SDF Download SDF
PubChem ID 16655129 Appearance Powder
Formula C13H13N3O2 M.Wt 243.3
Type of Compound N/A Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 4-(4-aminophenoxy)-N-methylpyridine-2-carboxamide
SMILES CNC(=O)C1=NC=CC(=C1)OC2=CC=C(C=C2)N
Standard InChIKey RXZZBPYPZLAEFC-UHFFFAOYSA-N
Standard InChI InChI=1S/C13H13N3O2/c1-15-13(17)12-8-11(6-7-16-12)18-10-4-2-9(14)3-5-10/h2-8H,14H2,1H3,(H,15,17)
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

4-(4-Aminophenoxy)-N-methyl-2-pyridinecarboxamide Dilution Calculator

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4-(4-Aminophenoxy)-N-methyl-2-pyridinecarboxamide Molarity Calculator

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Preparing Stock Solutions of 4-(4-Aminophenoxy)-N-methyl-2-pyridinecarboxamide

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.1102 mL 20.5508 mL 41.1015 mL 82.203 mL 102.7538 mL
5 mM 0.822 mL 4.1102 mL 8.2203 mL 16.4406 mL 20.5508 mL
10 mM 0.411 mL 2.0551 mL 4.1102 mL 8.2203 mL 10.2754 mL
50 mM 0.0822 mL 0.411 mL 0.822 mL 1.6441 mL 2.0551 mL
100 mM 0.0411 mL 0.2055 mL 0.411 mL 0.822 mL 1.0275 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on 4-(4-Aminophenoxy)-N-methyl-2-pyridinecarboxamide

Quantification of Sorafenib in Human Serum by Competitive Enzyme-Linked Immunosorbent Assay.[Pubmed:26521829]

Biol Pharm Bull. 2015;38(11):1788-93.

The multikinase inhibitor sorafenib has been used in the treatment of hepatocellular carcinoma, renal cell carcinoma, and differentiated thyroid carcinoma. Here we have demonstrated the production of the first specific antibody against sorafenib. Anti-sorafenib serum was obtained by immunizing mice with an antigen conjugated with bovine serum albumin and carboxylic modified 4-(4-Aminophenoxy)-N-methyl-2-pyridinecarboxamide (AMPC) using the N-succinimidyl ester method. Enzyme labeling of sorafenib with horseradish peroxidase was similarly performed using carboxylic modified AMPC. A simple competitive enzyme-linked immunosorbent assay (ELISA) for sorafenib was developed using the principle of direct competition between sorafenib and the enzyme marker for anti-sorafenib antibody, which had been adsorbed by the plastic surface of a microtiter plate. Serum sorafenib concentrations lower than 0.04 microg/mL were reproducibly measurable using the ELISA. This ELISA was specific to sorafenib and showed very slight cross-reactivity (2.5%) with a major metabolite, sorafenib N-oxide. The values of serum sorafenib levels from 32 patients measured by this ELISA were comparable with those measured by HPLC, and there was a strong correlation between the values determined by the two methods (Y=1.016X-0.137, r=0.979). The specificity and sensitivity of the ELISA for sorafenib should provide a valuable new tool for use in therapeutic drug monitoring and pharmacokinetic studies of sorafenib.

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