General
Preferred name
IBUDILAST
Synonyms
AV-411 ()
KC-404 ()
MN-166 ()
Ibudilast (KC-404) ()
KC-404, AV411, MN166 ()
AV411 ()
KETAS ()
Ibudilast-d7 ()
P&D ID
PD002711
CAS
50847-11-5
050847-11-5
2713301-45-0
Tags
available
drug
Approved by
PMDA
First approval
1989
Drug indication
Alcohol dependence
Methamphetamine dependence
Multiple sclerosis
Airway obstruction
Amyotrophic lateral sclerosis
Opioid dependence
Castleman's disease
Drug Status
approved
investigational
Max Phase
4.0
Probe control
Probe control not defined
Orthogonal probes
0
No orthogonal probes found
Similar probes
0
No structurally similar probes found
Structure formats
[[ format ]]
[[ compound[format === 'MOL' ? 'molblock' : format.toLowerCase()] ]]
Description
(extracted from source data)
DESCRIPTION
Ibudilast is a phosphodiesterase (PDE) inhibitor antiinflammatory drug. See the Biological activity tab for affinity data across a range of PDE isozymes.
(GtoPdb)
DESCRIPTION
Ibudilast (KC-404; AV-411; MN-166) is a cyclic AMP phosphodiesterase (PDE) inhibitor. Ibudilast has platelet anti-aggregatory effects. Ibudilast can be used for the research of asthma for its inhibitory effects on tracheal smooth muscle contractility. Ibudilast may be a useful neuroprotective and anti-dementia agent counteracting neurotoxicity in activated microglia[1].
PRICE
29
DESCRIPTION
Ibudilast has mechanisms that include anti-inflammatory effects, such as phosphodiesterase inhibition, and neuroprotective effects, such as inhibition of nitric oxide synthesis and reduction in reactive oxygen species.
(Enamine Bioactive Compounds)
DESCRIPTION
PDE inhibitor (non-selective)
(Tocriscreen Plus)
DESCRIPTION
Phosphodiesterase IV (PDE IV) inhibitor
(LOPAC library)
DESCRIPTION
PDE inhibitor (non-selective)
(Tocriscreen Total)
DESCRIPTION
Cyclooxygenase inhibitor; may be selective for COX-3
(Tocris Bioactive Compound Library)
DESCRIPTION
Ibudilast (MN-166)(KC-404;AV-411;MN-166) is a relatively nonselective phosphodiesterase inhibitor. It is approved for use as an anti-inflammatory in Japan.
(TargetMol Bioactive Compound Library)
[[ p.pathway_name ]]
[[ compound.targets[tid].gene_name ]]
Cell lines
0
Organisms
1
Compound Sets
35
AdooQ Bioactive Compound Library
ChEMBL Approved Drugs
ChEMBL 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
Concise Guide to Pharmacology 2025/26
CZ-OPENSCREEN Bioactive Library
Drug Repurposing Hub
DrugBank
DrugCentral
DrugCentral Approved Drugs
DrugMAP
DrugMAP Approved Drugs
DrugMatrix
Enamine Bioactive Compounds
EU-OPENSCREEN Bioactive Compound Library
EUbOPEN Chemogenomics Library
Guide to Pharmacology
JUMP-Target 1 Compound Set
LOPAC library
LSP-MoA library (Laboratory of Systems Pharmacology)
MedChem Express Bioactive Compound Library
Novartis Chemogenetic Library (NIBR MoA Box)
NPC Screening Collection
Prestwick Chemical Library
ReFrame library
Selleckchem Bioactive Compound Library
TargetMol Bioactive Compound Library
Tocris Bioactive Compound Library
Tocriscreen Plus
Tocriscreen Total
ZINC Tool Compounds
[[ a.name ]]
[[ ligand_id ]]
free of charge
External IDs
80
Molecular Weight
230.14
Hydrogen Bond Acceptors
3
Hydrogen Bond Donors
0
Rotatable Bonds
3
Ring Count
2
Aromatic Ring Count
2
cLogP
3.3
TPSA
34.37
Fraction CSP3
0.43
Chiral centers
0.0
Largest ring
6.0
QED
0.76
Structural alerts
0
No structural alerts detected
Custom attributes
(extracted from source data)
Target Type
Enzymes
Selectivity
PDE IV
Target
PDE
phosphodiesterase
IL1B, IL6, PDE3A, PDE4A, PDE4B, PDE4C, PDE4D, PDE5A
PDE4D
Phosphodiesterase (PDE)
Primary Target
Phosphodiesterases
MOA
Inhibitor
TLR4 (LPS) Receptor Antagonists
Leukotriene CysLT1 (LTD4) Antagonists
Phosphodiesterase Inhibitors
Mediator Release Inhibitors
leukotriene receptor antagonist, phosphodiesterase inhibitor
Member status
virtual
Indication
asthma, stroke
Disease Area
pulmonary, neurology/psychiatry
Pathway
Metabolism
Metabolic Enzyme/Protease
Recommended Cell Concentration
1 uM
Source data

