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Details

Stereochemistry RACEMIC
Molecular Formula C20H36N2O3S
Molecular Weight 384.576
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of IBUTILIDE

SMILES

CCCCCCCN(CC)CCCC(O)C1=CC=C(NS(C)(=O)=O)C=C1

InChI

InChIKey=ALOBUEHUHMBRLE-UHFFFAOYSA-N
InChI=1S/C20H36N2O3S/c1-4-6-7-8-9-16-22(5-2)17-10-11-20(23)18-12-14-19(15-13-18)21-26(3,24)25/h12-15,20-21,23H,4-11,16-17H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C20H36N2O3S
Molecular Weight 384.576
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 16:39:22 UTC 2023
Edited
by admin
on Sat Dec 16 16:39:22 UTC 2023
Record UNII
2436VX1U9B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
IBUTILIDE
INN   MI   VANDF   WHO-DD  
INN  
Official Name English
IBUTILIDE [VANDF]
Common Name English
ibutilide [INN]
Common Name English
IBUTILIDE [MI]
Common Name English
METHANESULFONAMIDE, N-(4-(4-(ETHYLHEPTYLAMINO)-1-HYDROXYBUTYL)PHENYL)-
Systematic Name English
Ibutilide [WHO-DD]
Common Name English
N-(4-(4-(ETHYL(HEPTYL)AMINO)-1-HYDROXYBUTYL)PHENYL)METHANESULFONAMIDE
Systematic Name English
Classification Tree Code System Code
NDF-RT N0000175426
Created by admin on Sat Dec 16 16:39:23 UTC 2023 , Edited by admin on Sat Dec 16 16:39:23 UTC 2023
NCI_THESAURUS C47793
Created by admin on Sat Dec 16 16:39:23 UTC 2023 , Edited by admin on Sat Dec 16 16:39:23 UTC 2023
WHO-ATC C01BD05
Created by admin on Sat Dec 16 16:39:23 UTC 2023 , Edited by admin on Sat Dec 16 16:39:23 UTC 2023
NCI_THESAURUS C93038
Created by admin on Sat Dec 16 16:39:23 UTC 2023 , Edited by admin on Sat Dec 16 16:39:23 UTC 2023
WHO-VATC QC01BD05
Created by admin on Sat Dec 16 16:39:23 UTC 2023 , Edited by admin on Sat Dec 16 16:39:23 UTC 2023
Code System Code Type Description
NCI_THESAURUS
C72581
Created by admin on Sat Dec 16 16:39:23 UTC 2023 , Edited by admin on Sat Dec 16 16:39:23 UTC 2023
PRIMARY
DRUG CENTRAL
1412
Created by admin on Sat Dec 16 16:39:23 UTC 2023 , Edited by admin on Sat Dec 16 16:39:23 UTC 2023
PRIMARY
DAILYMED
2436VX1U9B
Created by admin on Sat Dec 16 16:39:23 UTC 2023 , Edited by admin on Sat Dec 16 16:39:23 UTC 2023
PRIMARY
WIKIPEDIA
IBUTILIDE
Created by admin on Sat Dec 16 16:39:23 UTC 2023 , Edited by admin on Sat Dec 16 16:39:23 UTC 2023
PRIMARY
MESH
C067192
Created by admin on Sat Dec 16 16:39:23 UTC 2023 , Edited by admin on Sat Dec 16 16:39:23 UTC 2023
PRIMARY
DRUG BANK
DB00308
Created by admin on Sat Dec 16 16:39:23 UTC 2023 , Edited by admin on Sat Dec 16 16:39:23 UTC 2023
PRIMARY
ChEMBL
CHEMBL533
Created by admin on Sat Dec 16 16:39:23 UTC 2023 , Edited by admin on Sat Dec 16 16:39:23 UTC 2023
PRIMARY
RXCUI
41289
Created by admin on Sat Dec 16 16:39:23 UTC 2023 , Edited by admin on Sat Dec 16 16:39:23 UTC 2023
PRIMARY RxNorm
SMS_ID
100000083650
Created by admin on Sat Dec 16 16:39:23 UTC 2023 , Edited by admin on Sat Dec 16 16:39:23 UTC 2023
PRIMARY
INN
6642
Created by admin on Sat Dec 16 16:39:23 UTC 2023 , Edited by admin on Sat Dec 16 16:39:23 UTC 2023
PRIMARY
FDA UNII
2436VX1U9B
Created by admin on Sat Dec 16 16:39:23 UTC 2023 , Edited by admin on Sat Dec 16 16:39:23 UTC 2023
PRIMARY
IUPHAR
7200
Created by admin on Sat Dec 16 16:39:23 UTC 2023 , Edited by admin on Sat Dec 16 16:39:23 UTC 2023
PRIMARY
PUBCHEM
60753
Created by admin on Sat Dec 16 16:39:23 UTC 2023 , Edited by admin on Sat Dec 16 16:39:23 UTC 2023
PRIMARY
MERCK INDEX
m6191
Created by admin on Sat Dec 16 16:39:23 UTC 2023 , Edited by admin on Sat Dec 16 16:39:23 UTC 2023
PRIMARY Merck Index
EPA CompTox
DTXSID20861271
Created by admin on Sat Dec 16 16:39:23 UTC 2023 , Edited by admin on Sat Dec 16 16:39:23 UTC 2023
PRIMARY
EVMPD
SUB08102MIG
Created by admin on Sat Dec 16 16:39:23 UTC 2023 , Edited by admin on Sat Dec 16 16:39:23 UTC 2023
PRIMARY
HSDB
7926
Created by admin on Sat Dec 16 16:39:23 UTC 2023 , Edited by admin on Sat Dec 16 16:39:23 UTC 2023
PRIMARY
CAS
122647-31-8
Created by admin on Sat Dec 16 16:39:23 UTC 2023 , Edited by admin on Sat Dec 16 16:39:23 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
BINDER->LIGAND
BINDING
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Biological Half-life PHARMACOKINETIC
Volume of Distribution PHARMACOKINETIC