Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C15H11Cl2NO4 |
| Molecular Weight | 340.158 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)COC1=C(NC(=O)C2=CC(Cl)=C(Cl)C=C2)C=CC=C1
InChI
InChIKey=TVQRUKZAWSJVRX-UHFFFAOYSA-N
InChI=1S/C15H11Cl2NO4/c16-10-6-5-9(7-11(10)17)15(21)18-12-3-1-2-4-13(12)22-8-14(19)20/h1-7H,8H2,(H,18,21)(H,19,20)
Clamidoxic acid is a derivative of phenoxyacetic acid developed in the late 1950s by Smith and Nephew Research Ltd. Clamidoxic acid has been shown to have anti-inflammatory activity and low toxicity in animal tests. The compound was investigated in the clinical trials in patients suffering from rheumatoid arthritis and painful uncomplicated osteoarthritis of the hip, however, no further clinical development was reported.
Approval Year
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NCI_THESAURUS |
C257
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CHEMBL2104565
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C80539
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22554
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DTXSID30210711
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6170-69-0
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100000084597
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2299
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4H4JU6738Q
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C004685
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SUB06636MIG
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ACTIVE MOIETY
