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Details

Stereochemistry ACHIRAL
Molecular Formula C22H30N2O2S
Molecular Weight 386.551
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SUFENTANIL

SMILES

CCC(=O)N(C1=CC=CC=C1)C2(COC)CCN(CCC3=CC=CS3)CC2

InChI

InChIKey=GGCSSNBKKAUURC-UHFFFAOYSA-N
InChI=1S/C22H30N2O2S/c1-3-21(25)24(19-8-5-4-6-9-19)22(18-26-2)12-15-23(16-13-22)14-11-20-10-7-17-27-20/h4-10,17H,3,11-16,18H2,1-2H3

HIDE SMILES / InChI

Approval Year

Unknown
86413
Name Type Language
SUFENTANIL
EP   HSDB   INN   MART.   MI   USAN   VANDF   WHO-DD  
INN   USAN  
Official Name English
R-30730
Code English
N-[4-(Methoxymethyl)-1-[2-(2-thienyl)ethyl]-4-piperidyl]propionanilide
Systematic Name English
SUFENTANYL
Common Name English
R 30,730
Code English
SUFENTANIL [USAN]
Common Name English
Sufentanil [WHO-DD]
Common Name English
PROPANAMIDE, N-(4-(METHOXYMETHYL)-1-(2-(2-THIENYL)ETHYL)-4-PIPERIDINYL)-N-PHENYL-
Systematic Name English
SUFENTANIL [VANDF]
Common Name English
SUFENTANIL [MI]
Common Name English
SUFENTANIL [EP MONOGRAPH]
Common Name English
SUFENTANIL [HSDB]
Common Name English
SUFENTANIL [MART.]
Common Name English
sufentanil [INN]
Common Name English
IDS-NS-001
Code English
Classification Tree Code System Code
DEA NO. 9740
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
NCI_THESAURUS C67413
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
WHO-VATC QN01AH03
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
LIVERTOX 904
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
WIKIPEDIA List_of_fentanyl_analogues
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
WHO-ATC N01AH03
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
NDF-RT N0000175684
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
NDF-RT N0000175690
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
NCI_THESAURUS C1506
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
Code System Code Type Description
CHEBI
9316
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
PRIMARY
HSDB
6760
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
PRIMARY
IUPHAR
3534
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
PRIMARY
RXCUI
56795
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
PRIMARY RxNorm
WEB RESOURCE
SUFENTANIL
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
PRIMARY
SMS_ID
100000089189
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
PRIMARY
PUBCHEM
41693
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
PRIMARY
CAS
56030-54-7
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
PRIMARY
NCI_THESAURUS
C61956
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
PRIMARY
MERCK INDEX
m10288
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
PRIMARY Merck Index
INN
4048
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
PRIMARY
LACTMED
Sufentanil
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
PRIMARY
MESH
D017409
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
PRIMARY
DRUG CENTRAL
2491
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
PRIMARY
EPA CompTox
DTXSID6023604
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
PRIMARY
ChEMBL
CHEMBL658
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
PRIMARY
EVMPD
SUB10671MIG
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
PRIMARY
DAILYMED
AFE2YW0IIZ
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
PRIMARY
WIKIPEDIA
SUFENTANIL
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
PRIMARY Sufentanil first was synthesized at Janssen Pharmaceutica in 1974. Sufentanil is marketed for use by specialist centers under different trade names, such as Sufenta and Sufentil. Sufentanil with and without lidocaine or mepivacaine is available as a transdermal patch similar to Duragesic in Europe under trade names such as Chronogesic.
DRUG BANK
DB00708
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
PRIMARY
FDA UNII
AFE2YW0IIZ
Created by admin on Fri Dec 15 15:17:11 UTC 2023 , Edited by admin on Fri Dec 15 15:17:11 UTC 2023
PRIMARY
ACTIVE MOIETY
Structure of SUFENTANIL
METABOLITE (PARENT)
Structure of R-46570
METABOLITE INACTIVE (PARENT)
Structure of NORALFENTANIL
METABOLITE INACTIVE (PARENT)
Structure of N-PHENYLPROPANAMIDE
SALT/SOLVATE (PARENT)
Structure of SUFENTANIL HYDROCHLORIDE
SALT/SOLVATE (PARENT)
Structure of SUFENTANIL CITRATE
NIH
NCATS
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