Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C27H35NO5 |
Molecular Weight | 453.5705 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 7 / 7 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC[C@@](C)(O)[C@H]1C[C@@]23C=C[C@]1(OC)[C@@H]4OC5=C(OC(C)=O)C=CC6=C5[C@]24CCN(C)[C@@H]3C6
InChI
InChIKey=LFYBMMHFJIAKFE-PMEKXCSPSA-N
InChI=1S/C27H35NO5/c1-6-9-24(3,30)19-15-25-10-11-27(19,31-5)23-26(25)12-13-28(4)20(25)14-17-7-8-18(32-16(2)29)22(33-23)21(17)26/h7-8,10-11,19-20,23,30H,6,9,12-15H2,1-5H3/t19-,20-,23-,24-,25-,26+,27-/m1/s1
Acetorphine is a synthetic narcotic analgesic. Acetorphine was reported to have uses in veterinary medicine with pronounced advantages in the immobilization of the giraffe in which toxic effects were reduced as compared to the effects of etorphine. In July 1966, the Director-General of the World Health Organization informed the Secretary-General that WHO had arrived at the conclusion that etorphine and acetorphine should be included in Schedule I of the Convention, since they could give rise to similar abuse, and produce similar ill effects as the substances already listed therein. Acetorphine is a Schedule I controlled substance in the United States.
Approval Year
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C241
Created by
admin on Mon Mar 31 18:33:20 GMT 2025 , Edited by admin on Mon Mar 31 18:33:20 GMT 2025
|
||
|
DEA NO. |
9319
Created by
admin on Mon Mar 31 18:33:20 GMT 2025 , Edited by admin on Mon Mar 31 18:33:20 GMT 2025
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
ACETORPHINE
Created by
admin on Mon Mar 31 18:33:20 GMT 2025 , Edited by admin on Mon Mar 31 18:33:20 GMT 2025
|
PRIMARY | |||
|
DTXSID60905123
Created by
admin on Mon Mar 31 18:33:20 GMT 2025 , Edited by admin on Mon Mar 31 18:33:20 GMT 2025
|
PRIMARY | |||
|
2286
Created by
admin on Mon Mar 31 18:33:20 GMT 2025 , Edited by admin on Mon Mar 31 18:33:20 GMT 2025
|
PRIMARY | |||
|
SUB05226MIG
Created by
admin on Mon Mar 31 18:33:20 GMT 2025 , Edited by admin on Mon Mar 31 18:33:20 GMT 2025
|
PRIMARY | |||
|
2OGQ81529L
Created by
admin on Mon Mar 31 18:33:20 GMT 2025 , Edited by admin on Mon Mar 31 18:33:20 GMT 2025
|
PRIMARY | |||
|
20055090
Created by
admin on Mon Mar 31 18:33:20 GMT 2025 , Edited by admin on Mon Mar 31 18:33:20 GMT 2025
|
PRIMARY | |||
|
DB01469
Created by
admin on Mon Mar 31 18:33:20 GMT 2025 , Edited by admin on Mon Mar 31 18:33:20 GMT 2025
|
PRIMARY | |||
|
C79929
Created by
admin on Mon Mar 31 18:33:20 GMT 2025 , Edited by admin on Mon Mar 31 18:33:20 GMT 2025
|
PRIMARY | |||
|
100000084618
Created by
admin on Mon Mar 31 18:33:20 GMT 2025 , Edited by admin on Mon Mar 31 18:33:20 GMT 2025
|
PRIMARY | |||
|
CHEMBL2104593
Created by
admin on Mon Mar 31 18:33:20 GMT 2025 , Edited by admin on Mon Mar 31 18:33:20 GMT 2025
|
PRIMARY | |||
|
25333-77-1
Created by
admin on Mon Mar 31 18:33:20 GMT 2025 , Edited by admin on Mon Mar 31 18:33:20 GMT 2025
|
PRIMARY |
ACTIVE MOIETY
SALT/SOLVATE (PARENT)