Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C23H21NO4 |
| Molecular Weight | 375.4171 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCOC(NC1=CC=C(C=C1)C(O)=O)C(=O)C2=CC=C(C=C2)C3=CC=CC=C3
InChI
InChIKey=BPOMPTVRBWXZBY-UHFFFAOYSA-N
InChI=1S/C23H21NO4/c1-2-28-22(24-20-14-12-19(13-15-20)23(26)27)21(25)18-10-8-17(9-11-18)16-6-4-3-5-7-16/h3-15,22,24H,2H2,1H3,(H,26,27)
Xenazoic acid, an antiviral agent, was introduced in the early 1960s. Xenazoic acid might be of value in reducing the severity of meals infection if given early enough. Its use was associated with hepatic toxicity, which resulted in its withdrawal from the market in at least two countries (Belgium and France) in 1965. WHO has no information to suggest that xenazoic acid remains commercially available.
Approval Year
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NCI_THESAURUS |
C281
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58991
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CHEMBL1909289
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1174-11-4
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C66662
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43842
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SUB00101MIG
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100000079353
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59182
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KDU8VH09O8
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239062
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m532
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PRIMARY | Merck Index |
ACTIVE MOIETY
