1325559-19-0
1325559-19-0
Chemical Structure
Mefenamic acid-13C6
- CAS No.: 1325559-19-0
- Formula:C913C6H15NO2
- Molecular Weight:247.24
IUPAC Name: 2-((2,3-dimethylphenyl)amino)benzoic-1,2,3,4,5,6-13C6 acid
InChIKey: HYYBABOKPJLUIN-MQISJZSBSA-N
SMILES: OC([13C]([13CH]=[13CH][13CH]=[13CH]1)=[13C]1NC2=C(C(C)=CC=C2)C)=O
Biological Activity: Mefenamic acid-13C6 is the 13C-labeled Mefenamic acid. Mefenamic acid is a BBB-permeable non-steroidal anti-inflammatory agent, acting as a competitive inhibitor of hCOX-1 and hCOX-2, with IC50s of 40 nM and 3 μM for hCOX-1 and hCOX-2, respectively.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Mefenamic acid-13C6 | Mefenamic acid-13C6 is the 13C-labeled Mefenamic acid. Mefenamic acid is a BBB-permeable non-steroidal anti-inflammatory agent, acting as a competitive inhibitor of hCOX-1 and hCOX-2, with IC50s of 40 nM and 3 μM for hCOX-1 and hCOX-2, respectively. | |||||||||||||||||||||
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Mefenamic acid (Standard) | ≥98% | Mefenamic acid (Standard) is the analytical standard of Mefenamic acid. This product is intended for research and analytical applications. Mefenamic acid is a BBB-permeable non-steroidal anti-inflammatory agent, acting as a competitive inhibitor of hCOX-1 and hCOX-2, with IC50s of 40 nM and 3 μM for hCOX-1 and hCOX-2, respectively. | ||||||||||||||||||||
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Mefenamic Acid-d3 | Mefenamic Acid-d3 is the deuterium labeled Mefenamic acid. Mefenamic acid is a BBB-permeable non-steroidal anti-inflammatory agent, acting as a competitive inhibitor of hCOX-1 and hCOX-2, with IC50s of 40 nM and 3 μM for hCOX-1 and hCOX-2, respectively. | |||||||||||||||||||||
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Mefenamic acid-d4 | 98.0% | Mefenamic acid-d4 is a deuterium labeled Mefenamic acid. Mefenamic acid is a BBB-permeable non-steroidal anti-inflammatory agent, acting as a competitive inhibitor of hCOX-1 and hCOX-2, with IC50s of 40 nM and 3 μM for hCOX-1 and hCOX-2, respectively. | ||||||||||||||||||||
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Mefenamic acid | 99.95% | Mefenamic acid is a BBB-permeable and non-steroidal anti-inflammatory agent, acting as a competitive inhibitor of hCOX-1 and hCOX-2, with IC50s of 40 nM and 3 μM for hCOX-1 and hCOX-2, respectively. | ||||||||||||||||||||
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