Details
Stereochemistry | UNKNOWN |
Molecular Formula | C25H32N2O3.C2H2O4 |
Molecular Weight | 498.5681 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C(O)=O.CCC(=O)N(C1=CC=CC=C1)[C@@]2(CCN(CCC3=CC=CC=C3)C[C@@H]2C)C(=O)OC
InChI
InChIKey=CBKLICUQYUTWQL-XWGBWKJCSA-N
InChI=1S/C25H32N2O3.C2H2O4/c1-4-23(28)27(22-13-9-6-10-14-22)25(24(29)30-3)16-18-26(19-20(25)2)17-15-21-11-7-5-8-12-21;3-1(4)2(5)6/h5-14,20H,4,15-19H2,1-3H3;(H,3,4)(H,5,6)/t20-,25+;/m0./s1
Lofentanil is a pure mu-opioid receptor agonist derived from fentanyl. It is the most potent opioid to be administered to humans, about 500-1000 times more potent than morphine. Lofentanil provides a higher affinity quotient with longer dissociation times for the mu-receptors than fentanyl. The clinical study of the compound is difficult because there is a very individual sensibility. The appropriate doses are not easy to evaluate. Reversal of the loventanil depression needs very high and repeated naloxone dose. Practical use of lofentanil is limited. Lofentanil side effects are: nausea, vomiting and sedation.
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Activity of opioid ligands in cells expressing cloned mu opioid receptors. | 2003 Jan 4 |
|
Ligand-regulated internalization of the opioid receptor-like 1: a confocal study. | 2004 Jun |
|
Oral transmucosal fentanyl citrate in cancer pain management: a practical application of nanotechnology. | 2007 |
|
In vivo mechanisms precipitating torsades de pointes in a canine model of drug-induced long-QT1 syndrome. | 2007 Nov 1 |
|
The fentanyl/etomidate-anaesthetised beagle (FEAB) dog: a versatile in vivo model in cardiovascular safety research. | 2009 Jul-Aug |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6133403
Single doses: 0.25 ug, 0.50 ug and 0.75 ug
Route of Administration:
Intramuscular
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C67413
Created by
admin on Fri Dec 15 16:15:18 GMT 2023 , Edited by admin on Fri Dec 15 16:15:18 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
m1205
Created by
admin on Fri Dec 15 16:15:18 GMT 2023 , Edited by admin on Fri Dec 15 16:15:18 GMT 2023
|
PRIMARY | Merck Index | ||
|
C034846
Created by
admin on Fri Dec 15 16:15:18 GMT 2023 , Edited by admin on Fri Dec 15 16:15:18 GMT 2023
|
PRIMARY | |||
|
CHEMBL28198
Created by
admin on Fri Dec 15 16:15:18 GMT 2023 , Edited by admin on Fri Dec 15 16:15:18 GMT 2023
|
PRIMARY | |||
|
61380-41-4
Created by
admin on Fri Dec 15 16:15:18 GMT 2023 , Edited by admin on Fri Dec 15 16:15:18 GMT 2023
|
PRIMARY | |||
|
262-750-7
Created by
admin on Fri Dec 15 16:15:18 GMT 2023 , Edited by admin on Fri Dec 15 16:15:18 GMT 2023
|
PRIMARY | |||
|
DTXSID10976924
Created by
admin on Fri Dec 15 16:15:18 GMT 2023 , Edited by admin on Fri Dec 15 16:15:18 GMT 2023
|
PRIMARY | |||
|
6C1599T3OQ
Created by
admin on Fri Dec 15 16:15:18 GMT 2023 , Edited by admin on Fri Dec 15 16:15:18 GMT 2023
|
PRIMARY | |||
|
65498
Created by
admin on Fri Dec 15 16:15:18 GMT 2023 , Edited by admin on Fri Dec 15 16:15:18 GMT 2023
|
PRIMARY | |||
|
C80584
Created by
admin on Fri Dec 15 16:15:18 GMT 2023 , Edited by admin on Fri Dec 15 16:15:18 GMT 2023
|
PRIMARY |
ACTIVE MOIETY
SUBSTANCE RECORD