ibudilast 🐶 Veterinary Use | Indications/Contra | FAERs-F | FAERs-M | Orange Bk | PK/Tox | Related Drugs | BioActivity |

Stem definitionDrug idCAS RN
antiasthmatics or antiallergics, not acting primarily as antihistaminics anti-allergic or anti-inflammatory, not acting as anti-histaminics 1406 50847-11-5

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • ketas
  • KP-305
  • ibudilast
  • Molecular weight: 230.31
  • Formula: C14H18N2O
  • CLOGP: 3.41
  • LIPINSKI: 0
  • HAC: 3
  • HDO: 0
  • TPSA: 34.37
  • ALOGS: -3.11
  • ROTB: 3

Drug dosage:

None

ADMET properties:

None

Predicted pharmacokinetic/toxicological properties (PK-AZ):

PropertyDescriptionValueUnitConfidenceSimilarity
kinase-safety-class ACVR2A,ACVR2B,AXL,BRAF,CAMK2B,CAMK2D,CDK5,CDK9,DDR1,DYRK1B,EIF2AK3,ERBB2,FLT3,GRK2,ITK,MAP3K21,MAPK7,MARK4,NTRK2,PDK1,PDK2,PIK3CD,PRKDC,SIK2,STK33,TEK,TTK 27
kinase-selectivity-class AXL,BRAF 2
pfas-class PFAS structural alert (1 = True, 0 = False) 0

Approvals:

DateAgencyCompanyOrphan
May 1, 1989 PMDA Kyorin Pharmaceutical

FDA Adverse Event Reporting System (Female)

MedDRA adverse event termLikelihood ratioLikelihood ratio thresholdPatients taking drug having adverse eventPatients taking drug not having adverse eventPatients not taking drug having adverse eventPatients not taking drug not having adverse event
Body tinea 294.26 236.92 45 988 2103 90625311
Inhibitory drug interaction 269.69 236.92 44 989 3119 90624295
Infection susceptibility increased 267.14 236.92 45 988 3881 90623533
Poor quality sleep 258.36 236.92 59 974 24634 90602780

FDA Adverse Event Reporting System (Male)

None

FDA Adverse Event Reporting System (Geriatric)

MedDRA adverse event termLikelihood ratioLikelihood ratio thresholdPatients taking drug having adverse eventPatients taking drug not having adverse eventPatients not taking drug having adverse eventPatients not taking drug not having adverse event
Body tinea 293.77 137.66 44 1045 2071 110586139
Infection susceptibility increased 261.58 137.66 44 1045 4354 110583856
Inhibitory drug interaction 249.58 137.66 43 1046 4904 110583306
Poor quality sleep 248.51 137.66 57 1032 28020 110560190
Glucose tolerance impaired 226.21 137.66 44 1045 9793 110578417
Bone density decreased 204.75 137.66 44 1045 15998 110572212
Impaired quality of life 202.82 137.66 49 1040 29968 110558242
Impaired work ability 198.52 137.66 47 1042 26372 110561838
Purpura 196.95 137.66 46 1043 24342 110563868
Hyperlipidaemia 169.56 137.66 44 1045 35804 110552406
Oral herpes 169.28 137.66 44 1045 36036 110552174
Skin disorder 161.71 137.66 44 1045 42869 110545341
Cataract 139.02 137.66 45 1044 79440 110508770

FDA Adverse Event Reporting System (Pediatric)

None

Pharmacologic Action:

SourceCodeDescription
ATC R03DC04 RESPIRATORY SYSTEM
DRUGS FOR OBSTRUCTIVE AIRWAY DISEASES
OTHER SYSTEMIC DRUGS FOR OBSTRUCTIVE AIRWAY DISEASES
Leukotriene receptor antagonists
MeSH PA D001993 Bronchodilator Agents
MeSH PA D002317 Cardiovascular Agents
MeSH PA D004791 Enzyme Inhibitors
MeSH PA D006401 Hematologic Agents
MeSH PA D010726 Phosphodiesterase Inhibitors
MeSH PA D010975 Platelet Aggregation Inhibitors
MeSH PA D014665 Vasodilator Agents
MeSH PA D018373 Peripheral Nervous System Agents
MeSH PA D018927 Anti-Asthmatic Agents
MeSH PA D019141 Respiratory System Agents
CHEBI has role CHEBI:22587 antiviral agent
CHEBI has role CHEBI:35480 analgesic
CHEBI has role CHEBI:35610 antineoplastic agent
CHEBI has role CHEBI:35705 immunosuppressive agent
CHEBI has role CHEBI:149553 anticoronaviral agent

Related Drugs by ATC class:

R03DC Leukotriene receptor antagonists 3 drugs

Drug Use | Suggest Off label Use Form| |View source of the data|

DiseaseRelationSNOMED_IDDOID
Asthma indication 195967001 DOID:2841




🐶 Veterinary Drug Use

None

🐶 Veterinary products

None

Acid dissociation constants calculated using MoKa v3.0.0

Dissociation levelDissociation constantType (acidic/basic)
pKa1 3.86 Basic

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

TargetClassPharosUniProtActionTypeActivity value
(-log[M])
Mechanism
action
Bioact sourceMoA source
cGMP-inhibited 3',5'-cyclic phosphodiesterase A Enzyme IC50 5.80 CHEMBL
cAMP-specific 3',5'-cyclic phosphodiesterase 4B Enzyme IC50 7.19 CHEMBL
cGMP-specific 3',5'-cyclic phosphodiesterase Enzyme IC50 5.46 CHEMBL
cAMP-specific 3',5'-cyclic phosphodiesterase 4A Enzyme IC50 7.27 CHEMBL
cAMP-specific 3',5'-cyclic phosphodiesterase 4D Enzyme IC50 6.78 CHEMBL
cAMP-specific 3',5'-cyclic phosphodiesterase 4C Enzyme IC50 6.62 CHEMBL
cGMP-inhibited 3',5'-cyclic phosphodiesterase B Enzyme IC50 5.57 CHEMBL
Macrophage migration inhibitory factor Cytokine Kd 5.85 CHEMBL

External reference:

IDSource
D01385 KEGG_DRUG
C0123047 UMLSCUI
CHEBI:31684 CHEBI
CHEMBL19449 ChEMBL_ID
DB05266 DRUGBANK_ID
CHEMBL395091 ChEMBL_ID
3671 PUBCHEM_CID
C038366 MESH_SUPPLEMENTAL_RECORD_UI
7399 IUPHAR_LIGAND_ID
6068 INN_ID
M0TTH61XC5 UNII
010937 NDDF
AVL PDB_CHEM_ID
M0TTH61XC5 INXIGHT DRUGS

Pharmaceutical products:

None