Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C21H28N4O2 |
| Molecular Weight | 368.4726 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCO\N=C\C1=CC=C(OCCC2CCN(CC2)C3=NN=C(C)C=C3)C=C1
InChI
InChIKey=LNKHWGSSSPTTHB-CJLVFECKSA-N
InChI=1S/C21H28N4O2/c1-3-27-22-16-19-5-7-20(8-6-19)26-15-12-18-10-13-25(14-11-18)21-9-4-17(2)23-24-21/h4-9,16,18H,3,10-15H2,1-2H3/b22-16+
| Molecular Formula | C21H28N4O2 |
| Molecular Weight | 368.4726 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| In vitro activity of expanded-spectrum pyridazinyl oxime ethers related to pirodavir: novel capsid-binding inhibitors with potent antipicornavirus activity. | 2004-05 |
|
| An orally bioavailable oxime ether capsid binder with potent activity against human rhinovirus. | 2003-07-17 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:08:07 GMT 2025
by
admin
on
Mon Mar 31 22:08:07 GMT 2025
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| Record UNII |
3HYI9G51A5
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| Record Status |
Validated (UNII)
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| Record Version |
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3HYI9G51A5
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330600-86-7
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admin on Mon Mar 31 22:08:07 GMT 2025 , Edited by admin on Mon Mar 31 22:08:07 GMT 2025
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SUPERSEDED |
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|---|---|---|---|---|
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