Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C20H20N2O3S |
| Molecular Weight | 368.449 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1CCN(CC2=CC=C(OC3=NC4=C(S3)C=CC=C4)C=C2)CC1
InChI
InChIKey=BUZBVOKDNAZIIM-UHFFFAOYSA-N
InChI=1S/C20H20N2O3S/c23-19(24)15-9-11-22(12-10-15)13-14-5-7-16(8-6-14)25-20-21-17-3-1-2-4-18(17)26-20/h1-8,15H,9-13H2,(H,23,24)
| Molecular Formula | C20H20N2O3S |
| Molecular Weight | 368.449 |
| 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 |
|---|---|---|
| Attenuation of inflammation and cytokine production in rat colitis by a novel selective inhibitor of leukotriene A4 hydrolase. | 2008-03 |
|
| Anti-inflammatory activity of a potent, selective leukotriene A4 hydrolase inhibitor in comparison with the 5-lipoxygenase inhibitor zileuton. | 2007-06 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:03:24 GMT 2025
by
admin
on
Mon Mar 31 23:03:24 GMT 2025
|
| Record UNII |
7W7511NPF8
|
| Record Status |
Validated (UNII)
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| Record Version |
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841202-16-2
Created by
admin on Mon Mar 31 23:03:24 GMT 2025 , Edited by admin on Mon Mar 31 23:03:24 GMT 2025
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11245596
Created by
admin on Mon Mar 31 23:03:24 GMT 2025 , Edited by admin on Mon Mar 31 23:03:24 GMT 2025
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7W7511NPF8
Created by
admin on Mon Mar 31 23:03:24 GMT 2025 , Edited by admin on Mon Mar 31 23:03:24 GMT 2025
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PRIMARY |
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