CHEBI:61092 - 3-methylfentanyl

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ChEBI Name 3-methylfentanyl
ChEBI ID CHEBI:61092
Definition The monocarboxylic acid amide resulting from the formal condensation of the aryl amino group of 3-methyl-N-phenyl-1-(2-phenylethyl)piperidin-4-amine with propanoic acid.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C23H30N2O
Net Charge 0
Average Mass 350.49710
Monoisotopic Mass 350.236
InChI InChI=1S/C23H30N2O/c1-3-23(26)25(21-12-8-5-9-13-21)22-15-17-24(18-19(22)2)16-14-20-10-6-4-7-11-20/h4-13,19,22H,3,14-18H2,1-2H3
InChIKey MLQRZXNZHAOCHQ-UHFFFAOYSA-N
SMILES CCC(=O)N(C1CCN(CCc2ccccc2)CC1C)c1ccccc1
Roles Classification
Biological Role(s): opioid analgesic
A narcotic or opioid substance, synthetic or semisynthetic agent producing profound analgesia, drowsiness, and changes in mood.
mu-opioid receptor agonist
A compound that exhibits agonist activity at the mu-opioid receptor.
Application(s): sedative
A central nervous system depressant used to induce drowsiness or sleep or to reduce psychological excitement or anxiety.
opioid analgesic
A narcotic or opioid substance, synthetic or semisynthetic agent producing profound analgesia, drowsiness, and changes in mood.
mu-opioid receptor agonist
A compound that exhibits agonist activity at the mu-opioid receptor.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 3-methylfentanyl (CHEBI:61092) has role μ-opioid receptor agonist (CHEBI:55322)
3-methylfentanyl (CHEBI:61092) has role opioid analgesic (CHEBI:35482)
3-methylfentanyl (CHEBI:61092) has role sedative (CHEBI:35717)
3-methylfentanyl (CHEBI:61092) is a monocarboxylic acid amide (CHEBI:29347)
3-methylfentanyl (CHEBI:61092) is a piperidines (CHEBI:26151)
IUPAC Name
N-[3-methyl-1-(2-phenylethyl)piperidin-4-yl]-N-phenylpropanamide
Synonyms Sources
3-MF DrugBank
α-methylfentanyl ChEBI
mefentanyl DrugBank
N-(3-Methyl-1-(2-phenylethyl)-4-piperidinyl)-N-phenylpropanamide ChemIDplus
Manual Xref Database
DB01571 DrugBank
View more database links
Registry Numbers Types Sources
42045-86-3 CAS Registry Number ChemIDplus
42045-86-3 CAS Registry Number NIST Chemistry WebBook
495141 Reaxys Registry Number Reaxys
Citations Waiting for Citations Types Sources
16621415 PubMed citation Europe PMC
4712637 PubMed citation Europe PMC
Last Modified
05 March 2014