Page last updated: 2024-12-06

3-methylfentanyl

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth

Description

3-methylfentanyl: RN given refers to parent cpd without isomeric designation [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

3-methylfentanyl : 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. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

butyrfentanyl: a synthetic opioid; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID61996
CHEMBL ID4748291
CHEBI ID61092
SCHEMBL ID2337401
MeSH IDM0096647
PubMed CID621174
CHEMBL ID4759342
SCHEMBL ID18623773
MeSH IDM0096647

Synonyms (57)

Synonym
f 7209
propanamide, n-(3-methyl-1-(2-phenylethyl)-4-piperidinyl)-n-phenyl-
dea no. 9813
n-(3-methyl-1-(2-phenylethyl)-4-piperidinyl)-n-phenylpropanamide
n-(3-methyl-1-(2-phenylethyl)-4-piperidyl)-n-phenylpropanamide
r-26800
3-mf
mefentanyl
3-methylfentanyl
DB01571
42045-86-3
n-[3-methyl-1-(2-phenylethyl)piperidin-4-yl]-n-phenylpropanamide
CHEBI:61092 ,
unii-qvu94xe61a
hsdb 8379
qvu94xe61a ,
3-methylfentanil
EPITOPE ID:153511
SCHEMBL2337401
MLQRZXNZHAOCHQ-UHFFFAOYSA-N
n-(3-methyl-1-phenethyl-4-piperidyl)-n-phenylpropanamide
DTXSID30962228
Q2030844
CHEMBL4748291
PD008773
methyl-3-fentanyl
butanamide, n-phenyl-n-[1-(2-phenylethyl)-4-piperidinyl]-
1169-70-6
AKOS025243418
QQOMYEQLWQJRKK-UHFFFAOYSA-N
n-phenyl-n-[1-(2-phenylethyl)-4-piperidinyl]butanamide #
butyrylfentanyl
butanamide, n-phenyl-n-(1-(2-phenylethyl)-4-piperidinyl)-
butyrlfentanyl
n-butyrylfentanyl
nih-10486 free base
n-(1-phenethylpiperidin-4-yl)-n-phenylbutyramide
n-(1-phenethyl-4-piperidyl)-n-phenyl-butanamide
butyr-fentanyl
DB09173
butyrfentanyl
butyryl fentanyl
n-phenyl-n-(1-(2-phenylethyl)-4-piperidinyl)butanamide
butyryl-fentanyl
n-(1-phenylethyl)-4-piperidinyl)-n-phenylbutyramide
07V1H7R6ZN ,
unii-07v1h7r6zn
SCHEMBL18623773
CS-D0505
DTXSID30347410
1-(2-phenylethyl)-4-(n,n-butyrylphenylamino)piperidine
AS-48590
butyrfentanyl (butyrylfentanyl)
butyranilide, n-(1-phenethyl-4-piperidyl)- (7ci,8ci); n-phenyl-n-[1-(2-phenylethyl)-4-piperidinyl]butanamide; butyryl fentanyl; butyrfentanyl; butyrylfentanyl; n-phenyl-n-[1-(2-phenylethyl)piperidin-4-yl]butanamide
Q15408419
CHEMBL4759342
butyrylfentanyl, 1mg/ml in methanol

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
" When the C1 antibody was combined with an iodinated analog to fentanyl, good detectability of alpha-methylfentanyl and 3-methylfentanyl, in terms of fentanyl equivalents, was obtained from urine samples of dosed mares."( Pharmacologic effects and detection methods of methylated analogs of fentanyl in horses.
Blake, JW; Tai, CL; Tai, HH; Tobin, T; Weckman, TJ; Woods, WE, 1989
)
0.49
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
opioid analgesicA narcotic or opioid substance, synthetic or semisynthetic agent producing profound analgesia, drowsiness, and changes in mood.
mu-opioid receptor agonistA compound that exhibits agonist activity at the mu-opioid receptor.
sedativeA central nervous system depressant used to induce drowsiness or sleep or to reduce psychological excitement or anxiety.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (2)

ClassDescription
piperidines
monocarboxylic acid amideA carboxamide derived from a monocarboxylic acid.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (40)

TimeframeStudies, This Drug (%)All Drugs %
pre-199012 (30.00)18.7374
1990's11 (27.50)18.2507
2000's3 (7.50)29.6817
2010's10 (25.00)24.3611
2020's4 (10.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Reviews0 (0.00%)6.00%
Case Studies3 (8.57%)4.05%
Case Studies1 (10.00%)4.05%
Observational0 (0.00%)0.25%
Observational0 (0.00%)0.25%
Other32 (91.43%)84.16%
Other9 (90.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]