Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C25H32N2O2 |
Molecular Weight | 392.5338 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@@H](CN1CCOCC1)C(C(=O)N2CCCC2)(C3=CC=CC=C3)C4=CC=CC=C4
InChI
InChIKey=INUNXTSAACVKJS-NRFANRHFSA-N
InChI=1S/C25H32N2O2/c1-21(20-26-16-18-29-19-17-26)25(22-10-4-2-5-11-22,23-12-6-3-7-13-23)24(28)27-14-8-9-15-27/h2-7,10-13,21H,8-9,14-20H2,1H3/t21-/m0/s1
Molecular Formula | C25H32N2O2 |
Molecular Weight | 392.5338 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:21:04 GMT 2023
by
admin
on
Fri Dec 15 16:21:04 GMT 2023
|
Record UNII |
7M86YFN15D
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Code | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C67413
Created by
admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
|
||
|
DEA NO. |
9629
Created by
admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
730
Created by
admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
|
PRIMARY | |||
|
Levomoramide
Created by
admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
|
PRIMARY | |||
|
C018992
Created by
admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
|
PRIMARY | |||
|
10453145
Created by
admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
|
PRIMARY | |||
|
C83878
Created by
admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
|
PRIMARY | |||
|
SUB08481MIG
Created by
admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
|
PRIMARY | |||
|
100000082299
Created by
admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
|
PRIMARY | |||
|
DTXSID401016989
Created by
admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
|
PRIMARY | |||
|
227-123-4
Created by
admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
|
PRIMARY | |||
|
7M86YFN15D
Created by
admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
|
PRIMARY | |||
|
CHEMBL2104862
Created by
admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
|
PRIMARY | |||
|
5666-11-5
Created by
admin on Fri Dec 15 16:21:04 GMT 2023 , Edited by admin on Fri Dec 15 16:21:04 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
RACEMATE -> ENANTIOMER |
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |