Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C23H29NO3 |
| Molecular Weight | 367.4813 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 5 / 5 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC[C@H]1CC(=O)[C@@H]2OC3=C(OC)C=CC4=C3[C@@]25CCN(CC6CC6)[C@H](C4)[C@H]15
InChI
InChIKey=JMPUQJQXECRLKY-IKADHJCRSA-N
InChI=1S/C23H29NO3/c1-3-14-11-17(25)22-23-8-9-24(12-13-4-5-13)16(19(14)23)10-15-6-7-18(26-2)21(27-22)20(15)23/h6-7,13-14,16,19,22H,3-5,8-12H2,1-2H3/t14-,16+,19-,22-,23-/m0/s1
| Molecular Formula | C23H29NO3 |
| Molecular Weight | 367.4813 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 5 / 5 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Conorphone (TR5109) is an opioid of mixed agonist-antagonist analgesic class. In animal models, conorphone demonstrated an analgesic activity in the same range as morphine, and lack of addiction liability. Conoprphone was evaluated in a clinical trial for postoperative pain in the oral surgery model and in patients with postepisiotomy pain. The 40 mg dose of conorphone resulted in a significant incidence of side effects such as drowsiness, dizziness, nausea, and vomiting.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:42:37 GMT 2025
by
admin
on
Mon Mar 31 18:42:37 GMT 2025
|
| Record UNII |
9H58696D23
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C241
Created by
admin on Mon Mar 31 18:42:37 GMT 2025 , Edited by admin on Mon Mar 31 18:42:37 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
72060-05-0
Created by
admin on Mon Mar 31 18:42:37 GMT 2025 , Edited by admin on Mon Mar 31 18:42:37 GMT 2025
|
PRIMARY | |||
|
5361887
Created by
admin on Mon Mar 31 18:42:37 GMT 2025 , Edited by admin on Mon Mar 31 18:42:37 GMT 2025
|
PRIMARY | |||
|
4853
Created by
admin on Mon Mar 31 18:42:37 GMT 2025 , Edited by admin on Mon Mar 31 18:42:37 GMT 2025
|
PRIMARY | |||
|
9H58696D23
Created by
admin on Mon Mar 31 18:42:37 GMT 2025 , Edited by admin on Mon Mar 31 18:42:37 GMT 2025
|
PRIMARY | |||
|
SUB06804MIG
Created by
admin on Mon Mar 31 18:42:37 GMT 2025 , Edited by admin on Mon Mar 31 18:42:37 GMT 2025
|
PRIMARY | |||
|
C025489
Created by
admin on Mon Mar 31 18:42:37 GMT 2025 , Edited by admin on Mon Mar 31 18:42:37 GMT 2025
|
PRIMARY | |||
|
DTXSID501016499
Created by
admin on Mon Mar 31 18:42:37 GMT 2025 , Edited by admin on Mon Mar 31 18:42:37 GMT 2025
|
PRIMARY | |||
|
CHEMBL2110790
Created by
admin on Mon Mar 31 18:42:37 GMT 2025 , Edited by admin on Mon Mar 31 18:42:37 GMT 2025
|
PRIMARY | |||
|
100000084267
Created by
admin on Mon Mar 31 18:42:37 GMT 2025 , Edited by admin on Mon Mar 31 18:42:37 GMT 2025
|
PRIMARY | |||
|
C79935
Created by
admin on Mon Mar 31 18:42:37 GMT 2025 , Edited by admin on Mon Mar 31 18:42:37 GMT 2025
|
PRIMARY | |||
|
Conorfone
Created by
admin on Mon Mar 31 18:42:37 GMT 2025 , Edited by admin on Mon Mar 31 18:42:37 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
SALT/SOLVATE -> PARENT |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |