Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C21H24N4O2 |
| Molecular Weight | 364.4409 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCOC1=CC=CC=C1N2C(=O)C3=CC=CC=C3N=C2CN4CCNCC4
InChI
InChIKey=OBWOSMGNXYUDFB-UHFFFAOYSA-N
InChI=1S/C21H24N4O2/c1-2-27-19-10-6-5-9-18(19)25-20(15-24-13-11-22-12-14-24)23-17-8-4-3-7-16(17)21(25)26/h3-10,22H,2,11-15H2,1H3
| Molecular Formula | C21H24N4O2 |
| Molecular Weight | 364.4409 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 19:56:46 GMT 2023
by
admin
on
Sat Dec 16 19:56:46 GMT 2023
|
| Record UNII |
E6999JX933
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
Download
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Common Name | English |
| Code System | Code | Type | Description | ||
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11559627
Created by
admin on Sat Dec 16 19:56:46 GMT 2023 , Edited by admin on Sat Dec 16 19:56:46 GMT 2023
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903499-49-0
Created by
admin on Sat Dec 16 19:56:46 GMT 2023 , Edited by admin on Sat Dec 16 19:56:46 GMT 2023
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PRIMARY | |||
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E6999JX933
Created by
admin on Sat Dec 16 19:56:46 GMT 2023 , Edited by admin on Sat Dec 16 19:56:46 GMT 2023
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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TARGET -> INHIBITOR |
Reduces the amount of glutathione in cells which leads to ferroptosis. Mechanism assumed to be same as erastin.
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |
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