Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C23H29NO3.ClH |
| Molecular Weight | 403.942 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CCOC(=O)C1(CCN(CCC(O)C2=CC=CC=C2)CC1)C3=CC=CC=C3
InChI
InChIKey=HGEAGOBQOIMDQV-UHFFFAOYSA-N
InChI=1S/C23H29NO3.ClH/c1-2-27-22(26)23(20-11-7-4-8-12-20)14-17-24(18-15-23)16-13-21(25)19-9-5-3-6-10-19;/h3-12,21,25H,2,13-18H2,1H3;1H
PHENOPERIDINE is an opioid analgesic partly metabolized to meperidine in the liver. It is derived from pethidine by replacing the N methyl by a phenyl propanol chain. It is reputed to be a typical morphine-like analgesic characterized by its high potency, rapid onset of action, the intensity of its peak effect and the short duration of its pharmacological effects. It is used in general anesthesia.
Originator
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Motor neuropathy associated with cimetidine. | 1980 Oct 11 |
|
| Contemporary strategies to preserve renal function during cardiac and vascular surgery. | 2003 |
|
| The consolidation of neuroleptic therapy: Janssen, the discovery of haloperidol and its introduction into clinical practice. | 2009 Apr 29 |
Patents
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Brand Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Brand Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
31984
Created by
admin on Fri Dec 15 15:03:47 GMT 2023 , Edited by admin on Fri Dec 15 15:03:47 GMT 2023
|
PRIMARY | |||
|
100000085293
Created by
admin on Fri Dec 15 15:03:47 GMT 2023 , Edited by admin on Fri Dec 15 15:03:47 GMT 2023
|
PRIMARY | |||
|
1D9C1OK7KZ
Created by
admin on Fri Dec 15 15:03:47 GMT 2023 , Edited by admin on Fri Dec 15 15:03:47 GMT 2023
|
PRIMARY | |||
|
3627-49-4
Created by
admin on Fri Dec 15 15:03:47 GMT 2023 , Edited by admin on Fri Dec 15 15:03:47 GMT 2023
|
PRIMARY | |||
|
SUB03758MIG
Created by
admin on Fri Dec 15 15:03:47 GMT 2023 , Edited by admin on Fri Dec 15 15:03:47 GMT 2023
|
PRIMARY | |||
|
19260
Created by
admin on Fri Dec 15 15:03:47 GMT 2023 , Edited by admin on Fri Dec 15 15:03:47 GMT 2023
|
PRIMARY | |||
|
106508
Created by
admin on Fri Dec 15 15:03:47 GMT 2023 , Edited by admin on Fri Dec 15 15:03:47 GMT 2023
|
PRIMARY | RxNorm | ||
|
222-846-1
Created by
admin on Fri Dec 15 15:03:47 GMT 2023 , Edited by admin on Fri Dec 15 15:03:47 GMT 2023
|
PRIMARY | |||
|
DTXSID10957657
Created by
admin on Fri Dec 15 15:03:47 GMT 2023 , Edited by admin on Fri Dec 15 15:03:47 GMT 2023
|
PRIMARY | |||
|
m8632
Created by
admin on Fri Dec 15 15:03:47 GMT 2023 , Edited by admin on Fri Dec 15 15:03:47 GMT 2023
|
PRIMARY | Merck Index |
PARENT (SALT/SOLVATE)
SUBSTANCE RECORD
