General
Preferred name
IBUTILIDE
Synonyms
Ibutilide hemifumarate ()
U-70226E ()
Corvert ()
Corvert Fumarate ()
U70226E ()
Ibutilide Fumarate ()
Ibutilide hemifumarate ()
2016-03-02: ibutilide fumarate ()
Ibutilide (fumarate) ()
U70226E (free base) ()
U-70226E,Corvert Fumarate ()
Fumaric acid compound with N-(4-(4-(ethyl(heptyl)amino)-1-hydroxybutyl)phenyl)methanesulfonamide and ()
(±)-Ibutilide (hemifumarate) ()
Ibutilida ()
P&D ID
PD010110
CAS
122647-32-9
122647-31-8
100632-81-3
Tags
available
drug
Approved by
FDA
First approval
1995
Drug indication
Atrial fibrillation
cardiac arrhythmia
Drug Status
approved
Max Phase
4.0
Structure
Probe scores
P&D probe-likeness score
[[ v.score ]]%
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
PRICE 65
DESCRIPTION Ibutilide is an antiarrhythmic drug.
Marketed formulations may contain ibutilide fumarate (PubChem CID 6437366). (GtoPdb)
DESCRIPTION Ibutilide (U70226E free base), an action potential-prolonging antiarrhythmic, is a potent blocker of the rapidly activating delayed rectifier K+ current (IKr) in AT-1 cells[1].
DESCRIPTION Ibutilide (U70226E) fumarate, an action potential-prolonging antiarrhythmic, is a potent blocker of the rapidly activating delayed rectifier K+ current (IKr) in AT-1 cells[1].
DESCRIPTION TRPA1 blocker (Tocris Bioactive Compound Library)
DESCRIPTION Blocks IKr, hERG and L-type Ca2+ channels; class III antiarrhythmic (Tocriscreen Plus)
DESCRIPTION Ibutilide is a class III antiarrhythmic agent used to correct atrial fibrillation and atrial flutter, which can be considered as an alternative to cardioversion. (Enamine Bioactive Compounds)
DESCRIPTION Ibutilide Fumarate (U70226E) is the fumarate salt form of ibutilide, a class III antiarrhythmic agent. Ibutilide exerts its effect by activating a slow, inward, predominately sodium current rather than by blocking outward potassium currents. This results in prolongation of atrial and ventricular action potential duration and refractory periods. Ibutilide slightly decreases the sinus rate and atrioventricular (AV) conduction and produces a dose-related prolongation of the QT interval. (TargetMol Bioactive Compound Library)
Compound Sets
33
AdooQ Bioactive Compound Library
Cayman Chemical Bioactives
CeMM library of unique drugs (CLOUD)
ChEMBL Approved Drugs
Concise Guide to Pharmacology 2017/18
Concise Guide to Pharmacology 2019/20
Concise Guide to Pharmacology 2021/22
Concise Guide to Pharmacology 2023/24
CZ-OPENSCREEN Bioactive Library
DrugBank
DrugBank Approved Drugs
DrugCentral
DrugCentral Approved Drugs
DrugMAP
DrugMAP Approved Drugs
DrugMatrix
Enamine Bioactive Compounds
Enamine BioReference Compounds
Guide to Pharmacology
JUMP-Target 1 Compound Set
LSP-MoA library (Laboratory of Systems Pharmacology)
MedChem Express Bioactive Compound Library
NCATS Inxight Approved Drugs
Novartis Chemogenetic Library (NIBR MoA Box)
NPC Screening Collection
Other bioactive compounds
Prestwick Chemical Library
ReFrame library
Selleckchem Bioactive Compound Library
TargetMol Bioactive Compound Library
Tocris Bioactive Compound Library
Tocriscreen Plus
External IDs
64
Properties
(calculated by RDKit )
Molecular Weight
384.24
Hydrogen Bond Acceptors
4
Hydrogen Bond Donors
2
Rotatable Bonds
14
Ring Count
1
Aromatic Ring Count
1
cLogP
4.16
TPSA
69.64
Fraction CSP3
0.7
Chiral centers
1.0
Largest ring
6.0
QED
0.47
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Target Type
Ion Channels
MOA
voltage-gated potassium channel blocker
Potassium Channel Blockers
Antiarrhythmic
Target
HERG
Calcium Channel
Sodium Channel
KCNK1
Potassium Channel
Primary Target
Other Channel Modulators
Member status
member
Therapeutic Class
Antiarrhythmic Agents
Pathway
Membrane Transporter/Ion Channel
Metabolism
Source data