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-WCWDXBQESA-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 17:29:59 UTC 2023
by
admin
on
Sat Dec 16 17:29:59 UTC 2023
|
| Record UNII |
UI9AT88BS7
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
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1394929-55-5
Created by
admin on Sat Dec 16 17:29:59 UTC 2023 , Edited by admin on Sat Dec 16 17:29:59 UTC 2023
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PRIMARY | |||
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UI9AT88BS7
Created by
admin on Sat Dec 16 17:29:59 UTC 2023 , Edited by admin on Sat Dec 16 17:29:59 UTC 2023
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PRIMARY | |||
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60202715
Created by
admin on Sat Dec 16 17:29:59 UTC 2023 , Edited by admin on Sat Dec 16 17:29:59 UTC 2023
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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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 | |||
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METABOLIC ENZYME -> INHIBITOR |
E-Norendoxifen inhibited CYP3A4 3.7-fold more potently than Z-norendoxifen.
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