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CHEBI:61092 - 3-methylfentanyl
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ChEBI Ontology
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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.
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Formula
C23H30N2O
Net Charge
0
Average Mass
350.49710
Monoisotopic Mass
350.23581
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
Types
Sources
16621415
PubMed citation
Europe PMC
4712637
PubMed citation
Europe PMC
Last Modified
05 March 2014