Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C24H25NO2 |
| Molecular Weight | 359.4608 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC\C(=C(/C1=CC=C(O)C=C1)C2=CC=C(OCCN)C=C2)C3=CC=CC=C3
InChI
InChIKey=YCQBLTPGQSYLHD-VHXPQNKSSA-N
InChI=1S/C24H25NO2/c1-2-23(18-6-4-3-5-7-18)24(19-8-12-21(26)13-9-19)20-10-14-22(15-11-20)27-17-16-25/h3-15,26H,2,16-17,25H2,1H3/b24-23-
| Molecular Formula | C24H25NO2 |
| Molecular Weight | 359.4608 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Optical Activity | NONE |
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 17:56:42 GMT 2023
by
admin
on
Sat Dec 16 17:56:42 GMT 2023
|
| Record UNII |
51GJD354B5
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
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Common Name | English | ||
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Systematic Name | English |
| Code System | Code | Type | Description | ||
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1308808-22-1
Created by
admin on Sat Dec 16 17:56:43 GMT 2023 , Edited by admin on Sat Dec 16 17:56:43 GMT 2023
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PRIMARY | |||
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DTXSID701337073
Created by
admin on Sat Dec 16 17:56:43 GMT 2023 , Edited by admin on Sat Dec 16 17:56:43 GMT 2023
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PRIMARY | |||
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68037237
Created by
admin on Sat Dec 16 17:56:43 GMT 2023 , Edited by admin on Sat Dec 16 17:56:43 GMT 2023
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PRIMARY | |||
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1217237-98-3
Created by
admin on Sat Dec 16 17:56:43 GMT 2023 , Edited by admin on Sat Dec 16 17:56:43 GMT 2023
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NON-SPECIFIC STEREOCHEMISTRY | |||
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51GJD354B5
Created by
admin on Sat Dec 16 17:56:43 GMT 2023 , Edited by admin on Sat Dec 16 17:56:43 GMT 2023
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PRIMARY | |||
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Norendoxifen
Created by
admin on Sat Dec 16 17:56:43 GMT 2023 , Edited by admin on Sat Dec 16 17:56:43 GMT 2023
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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METABOLIC ENZYME -> INHIBITOR | |||
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METABOLIC ENZYME -> INHIBITOR |
E-Norendoxifen inhibited CYP1A2 2.0-fold more potently than Z-norendoxifen.
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METABOLIC ENZYME -> INHIBITOR |
E-Norendoxifen inhibited CYP3A4 3.7-fold more potently than Z-norendoxifen.
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METABOLIC ENZYME -> INHIBITOR |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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PARENT -> METABOLITE |
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