U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry MIXED
Molecular Formula C21H28N2OS
Molecular Weight 356.525
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-METHYLTHIOFENTANYL

SMILES

CCC(=O)N(C1CCN(CCC2=CC=CS2)CC1C)C3=CC=CC=C3

InChI

InChIKey=SRARDYUHGVMEQI-UHFFFAOYSA-N
InChI=1S/C21H28N2OS/c1-3-21(24)23(18-8-5-4-6-9-18)20-12-14-22(16-17(20)2)13-11-19-10-7-15-25-19/h4-10,15,17,20H,3,11-14,16H2,1-2H3

HIDE SMILES / InChI

Approval Year

Unknown
139594
Targets

Targets

Primary TargetPharmacologyConditionPotency
Mu-type opioid receptor
61
Target ID: P35372|||G8XRH8|||Q5TDA1|||Q9UN57
Gene ID: 4988.0
Gene Symbol: OPRM1
Target Organism: Homo sapiens (Human)
Agonist
2678
Kappa-type opioid receptor
60
Target ID: P41145
Gene ID: 4986.0
Gene Symbol: OPRK1
Target Organism: Homo sapiens (Human)
Agonist
2678
Delta-type opioid receptor
45
Target ID: P41143
Gene ID: 4985.0
Gene Symbol: OPRD1
Target Organism: Homo sapiens (Human)
Agonist
2678
PubMed

PubMed

TitleDatePubMed
Development of an enzyme-linked immunosorbent assay for fentanyl and applications of fentanyl antibody-coated nanoparticles for sample preparation.
2006 Jun 16
Patents

Patents

20130041028
3
Name Type Language
3-METHYLTHIOFENTANYL
Common Name English
J472.964A
Code English
3-METHYLTHIOFENTANIL
Common Name English
IDS-NM-024
Code English
PROPANAMIDE, N-(3-METHYL-1-(2-(2-THIENYL)ETHYL)-4-PIPERIDINYL)-N-PHENYL-
Systematic Name English
IDS-NM-024(SECT.3)
Code English
N-(3-METHYL-1-(2-THIENYL)ETHYL-4-PIPERIDINYL)-N-PHENYLPROPANAMIDE
Systematic Name English
Classification Tree Code System Code
DEA NO. 9833
Created by admin on Sat Dec 16 09:34:56 GMT 2023 , Edited by admin on Sat Dec 16 09:34:56 GMT 2023
WIKIPEDIA List_of_fentanyl_analogues
Created by admin on Sat Dec 16 09:34:56 GMT 2023 , Edited by admin on Sat Dec 16 09:34:56 GMT 2023
Code System Code Type Description
PUBCHEM
62296
Created by admin on Sat Dec 16 09:34:56 GMT 2023 , Edited by admin on Sat Dec 16 09:34:56 GMT 2023
PRIMARY
CHEBI
53763
Created by admin on Sat Dec 16 09:34:56 GMT 2023 , Edited by admin on Sat Dec 16 09:34:56 GMT 2023
PRIMARY
EPA CompTox
DTXSID60861311
Created by admin on Sat Dec 16 09:34:56 GMT 2023 , Edited by admin on Sat Dec 16 09:34:56 GMT 2023
PRIMARY
CAS
86052-04-2
Created by admin on Sat Dec 16 09:34:56 GMT 2023 , Edited by admin on Sat Dec 16 09:34:56 GMT 2023
PRIMARY
WIKIPEDIA
3-METHYLTHIOFENTANYL
Created by admin on Sat Dec 16 09:34:56 GMT 2023 , Edited by admin on Sat Dec 16 09:34:56 GMT 2023
PRIMARY 3-Methyl-thiofentanyl has similar effects to fentanyl. Side effects of fentanyl analogs are similar to those of fentanyl itself, which include itching, nausea and potentially serious respiratory depression, which can be life-threatening. Fentanyl analogs have killed hundreds of people throughout Europe and the former Soviet republics since the most recent resurgence in use began in Estonia in the early 2000s, and novel derivatives continue to appear.
FDA UNII
C9C204973M
Created by admin on Sat Dec 16 09:34:56 GMT 2023 , Edited by admin on Sat Dec 16 09:34:56 GMT 2023
PRIMARY
DRUG BANK
DB01439
Created by admin on Sat Dec 16 09:34:56 GMT 2023 , Edited by admin on Sat Dec 16 09:34:56 GMT 2023
PRIMARY
WEB RESOURCE
3-METHYLTHIOFENTANYL
Created by admin on Sat Dec 16 09:34:56 GMT 2023 , Edited by admin on Sat Dec 16 09:34:56 GMT 2023
PRIMARY
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
For language access assistance, contact the NCATS Public Information Officer
National Center for Advancing Translational Sciences (NCATS),
6701 Democracy Boulevard, Bethesda MD 20892-4874 • 301-594-8966