Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C27H26ClN3O5 |
| Molecular Weight | 507.965 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=C(C=C1)N2N=C(C=C2C3=CC=C(OC)C=C3)C(OC)(OC)C4=CC=C(Cl)C(=C4)C(N)=O
InChI
InChIKey=USJVSASRKOHVHQ-UHFFFAOYSA-N
InChI=1S/C27H26ClN3O5/c1-33-20-10-5-17(6-11-20)24-16-25(30-31(24)19-8-12-21(34-2)13-9-19)27(35-3,36-4)18-7-14-23(28)22(15-18)26(29)32/h5-16H,1-4H3,(H2,29,32)
| Molecular Formula | C27H26ClN3O5 |
| Molecular Weight | 507.965 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Effects of dual inhibitor of cyclooxygenase and 5-lipoxygenase on acute necrotizing pancreatitis in rats. | 2006-09-26 |
|
| ER-34122, a novel dual 5-lipoxygenase/cyclooxygenase inhibitor with potent anti-inflammatory activity in an arachidonic acid-induced ear inflammation model. | 1998-10 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:36:09 GMT 2025
by
admin
on
Mon Mar 31 23:36:09 GMT 2025
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| Record UNII |
72Y1B3J8FS
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| Record Status |
Validated (UNII)
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| Record Version |
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72Y1B3J8FS
Created by
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9892473
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admin on Mon Mar 31 23:36:09 GMT 2025 , Edited by admin on Mon Mar 31 23:36:09 GMT 2025
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179325-62-3
Created by
admin on Mon Mar 31 23:36:09 GMT 2025 , Edited by admin on Mon Mar 31 23:36:09 GMT 2025
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