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=CC=CC=C1NC(=O)C2=CC=C(Cl)C(Cl)=C2
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)
| Molecular Formula | C15H11Cl2NO4 |
| Molecular Weight | 340.158 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
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
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 09:30:40 GMT 2025
by
admin
on
Wed Apr 02 09:30:40 GMT 2025
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| Record UNII |
4H4JU6738Q
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| Record Status |
Validated (UNII)
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| Record Version |
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Official Name | English | ||
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Preferred Name | English | ||
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Common Name | English | ||
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Code | English | ||
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Systematic Name | English |
| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C257
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admin on Wed Apr 02 09:30:40 GMT 2025 , Edited by admin on Wed Apr 02 09:30:40 GMT 2025
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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
Created by
admin on Wed Apr 02 09:30:40 GMT 2025 , Edited by admin on Wed Apr 02 09:30:40 GMT 2025
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |