1189707-81-0

Mefenamic Acid-d<sub>3</sub> Chemical Structure
1189707-81-0

Chemical Structure

Mefenamic Acid-d3

  • CAS. Nr.: 1189707-81-0
  • Formula:C15H12D3NO2
  • Molecular Weight:244.30

IUPAC Name: 2-((2-methyl-3-(methyl-d3)phenyl)amino)benzoic acid

InChIKey: HYYBABOKPJLUIN-FIBGUPNXSA-N

SMILES: N(C1=C(C(O)=O)C=CC=C1)C2=C(C)C(C([2H])([2H])[2H])=CC=C2

Biological Activity: 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.

Art. -Nr. Produktname Reinheit Beschreibung Pricing
HY-B0574S1
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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HY-B0574R
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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HY-B0574S
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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HY-B0574S2
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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HY-B0574
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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