Drug General Information |
Drug ID |
D0HC3H
|
Former ID |
DNC012107
|
Drug Name |
Dimepheptanol
|
Drug Type |
Small molecular drug
|
Indication |
Discovery agent
|
Investigative |
[1]
|
Structure |
|
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2D MOL
3D MOL
|
Formula |
C21H29NO
|
Canonical SMILES |
CCC(C(CC(C)N(C)C)(C1=CC=CC=C1)C2=CC=CC=C2)O
|
InChI |
1S/C21H29NO/c1-5-20(23)21(16-17(2)22(3)4,18-12-8-6-9-13-18)19-14-10-7-11-15-19/h6-15,17,20,23H,5,16H2,1-4H3
|
InChIKey |
QIRAYNIFEOXSPW-UHFFFAOYSA-N
|
CAS Number |
CAS 545-90-4
|
PubChem Compound ID |
|
Target and Pathway |
Target(s) |
Mu-type opioid receptor |
Target Info |
Inhibitor |
[1]
|
Delta-type opioid receptor |
Target Info |
Inhibitor |
[1]
|
Kappa-type opioid receptor |
Target Info |
Inhibitor |
[1]
|
KEGG Pathway
|
Neuroactive ligand-receptor interaction
|
Estrogen signaling pathway
|
Morphine addictionhsa04022:cGMP-PKG signaling pathway
|
Sphingolipid signaling pathway
|
Neuroactive ligand-receptor interactionhsa04080:Neuroactive ligand-receptor interaction
|
NetPath Pathway
|
TCR Signaling Pathway
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PANTHER Pathway
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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
|
Enkephalin release
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Opioid proenkephalin pathway
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Opioid proopiomelanocortin pathwayP00026:Heterotrimeric G-protein signaling pathway-Gi alpha and Gs alpha mediated pathway
|
Opioid prodynorphin 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. 1981 Jul;24(7):903-6.Synthesis of analogues of acetylmethadol and methadol as potential narcotic antagonists. |