Drug General Information |
Drug ID |
D0L6QN
|
Former ID |
DNC011480
|
Drug Name |
LOFENTANIL
|
Drug Type |
Small molecular drug
|
Indication |
Discovery agent
|
Investigative |
[1]
|
Structure |
|
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2D MOL
3D MOL
|
Formula |
C27H34N2O7
|
Canonical SMILES |
CCC(=O)N(C1=CC=CC=C1)C2(CCN(CC2C)CCC3=CC=CC=C3)C(=O)OC
|
InChI |
1S/C25H32N2O3/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/h5-14,20H,4,15-19H2,1-3H3
|
InChIKey |
IMYHGORQCPYVBZ-UHFFFAOYSA-N
|
CAS Number |
CAS 61380-40-3
|
PubChem Compound ID |
|
Target and Pathway |
Target(s) |
Mu-type opioid receptor |
Target Info |
Inhibitor |
[1]
|
Kappa-type opioid receptor |
Target Info |
Inhibitor |
[1]
|
Delta-type opioid receptor |
Target Info |
Inhibitor |
[1]
|
KEGG Pathway
|
Neuroactive ligand-receptor interaction
|
Estrogen signaling pathway
|
Morphine addictionhsa04080:Neuroactive ligand-receptor interactionhsa04022:cGMP-PKG signaling pathway
|
Sphingolipid signaling pathway
|
NetPath Pathway
|
TCR Signaling Pathway
|
PANTHER Pathway
|
Heterotrimeric G-protein signaling pathway-Gi alpha and Gs alpha mediated pathway
|
Heterotrimeric G-protein signaling pathway-Gq alpha and Go alpha mediated pathway
|
Enkephalin releaseP00026:Heterotrimeric G-protein signaling pathway-Gi alpha and Gs alpha mediated pathway
|
Opioid prodynorphin pathwayP00026:Heterotrimeric G-protein signaling pathway-Gi alpha and Gs alpha mediated pathway
|
Enkephalin release
|
Opioid proenkephalin pathway
|
Opioid proopiomelanocortin pathway
|
Pathway Interaction Database
|
IL4-mediated signaling events
|
Reactome
|
Peptide ligand-binding receptors
|
G alpha (i) signalling eventsR-HSA-375276:Peptide ligand-binding receptors
|
G alpha (i) signalling events
|
WikiPathways
|
TCR Signaling Pathway
|
GPCRs, Class A Rhodopsin-like
|
Peptide GPCRs
|
Opioid Signalling
|
GPCR ligand binding
|
GPCR downstream signalingWP455:GPCRs, Class A Rhodopsin-like
|
GPCR downstream signaling
|
References |
REF 1 | J Med Chem. 1982 Aug;25(8):913-9.Potential affinity labels for the opiate receptor based on fentanyl and related compounds. |