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
Wed Apr 02 09:50:29 GMT 2025
by
admin
on
Wed Apr 02 09:50:29 GMT 2025
|
| Record UNII |
51GJD354B5
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
1308808-22-1
Created by
admin on Wed Apr 02 09:50:29 GMT 2025 , Edited by admin on Wed Apr 02 09:50:29 GMT 2025
|
PRIMARY | |||
|
DTXSID701337073
Created by
admin on Wed Apr 02 09:50:29 GMT 2025 , Edited by admin on Wed Apr 02 09:50:29 GMT 2025
|
PRIMARY | |||
|
68037237
Created by
admin on Wed Apr 02 09:50:29 GMT 2025 , Edited by admin on Wed Apr 02 09:50:29 GMT 2025
|
PRIMARY | |||
|
1217237-98-3
Created by
admin on Wed Apr 02 09:50:29 GMT 2025 , Edited by admin on Wed Apr 02 09:50:29 GMT 2025
|
NON-SPECIFIC STEREOCHEMISTRY | |||
|
51GJD354B5
Created by
admin on Wed Apr 02 09:50:29 GMT 2025 , Edited by admin on Wed Apr 02 09:50:29 GMT 2025
|
PRIMARY | |||
|
Norendoxifen
Created by
admin on Wed Apr 02 09:50:29 GMT 2025 , Edited by admin on Wed Apr 02 09:50:29 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
METABOLIC ENZYME -> INHIBITOR | |||
|
METABOLIC ENZYME -> INHIBITOR |
E-Norendoxifen inhibited CYP1A2 2.0-fold more potently than Z-norendoxifen.
|
||
|
METABOLIC ENZYME -> INHIBITOR |
E-Norendoxifen inhibited CYP3A4 3.7-fold more potently than Z-norendoxifen.
|
||
|
METABOLIC ENZYME -> INHIBITOR |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
PARENT -> METABOLITE |
|