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

Stem definitionDrug idCAS RN
1683 58-27-5

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • menadione
  • menaquinone
  • menadion
  • menaphthon
  • menaphthone
  • 2-Methyl-1,4-naphthalenedione
  • Molecular weight: 172.18
  • Formula: C11H8O2
  • CLOGP: 2.13
  • LIPINSKI: 0
  • HAC: 2
  • HDO: 0
  • TPSA: 34.14
  • ALOGS: -2.53
  • ROTB: 0

  • Status: OFM

  • Legend:
    OFP - off patent
    OFM - off market
    ONP - on patent

Drug dosage:

DoseUnitRoute
10 mg O
2 mg P

ADMET properties:

None

Predicted pharmacokinetic/toxicological properties (PK-AZ):

PropertyDescriptionValueUnitConfidenceSimilarity
kinase-safety-class ACVR2A,ACVR2B,ACVRL1,AKT2,AKT3,ALK,AURKA,AURKB,AXL,BRAF,BTK,CAMK2B,CAMK2D,CDK1,CDK4,CDK5,CDK9,CHEK1,CSF1R,DDR1,DYRK1B,EIF2AK3,EPHB4,ERBB2,FLT3,GRK2,GRK3,GSK3B,IKBKB,ITK,JAK1,JAK2,KIT,MAP2K6,MAP3K1,MAP3K14,MAP3K21,MAP3K7,MAP4K1,MAP4K3,MAPK1,MAPK10,MAPK12,MAPK7,MAPK9,MAPKAPK2,MARK4,MELK,MET,MTOR,NTRK2,PAK4,PDK1,PDK2,PDK4,PDPK1,PIK3CB,PIK3CD,PIM1,PIM2,PLK1,PLK2,PLK3,PLK4,PRKCD,PRKDC,SGK1,SIK2,SIK3,STK33,SYK,TEK,TTK,ULK1,ULK2 75
kinase-selectivity-class ACVR2A,ACVR2B,AURKB,AXL,BRAF,CAMK2D,CDK4,CDK9,DDR1,DYRK1B,EIF2AK3,EPHB4,ERBB2,GRK2,GSK3A,MAP2K3,MAP2K6,MAP3K14,MAPK1,MAPK12,MAPK7,MARK4,MET,PIK3CB,PIK3CD,PRKDC,SIK2,STK33,TEK,TTK,ULK1 31
pfas-class PFAS structural alert (1 = True, 0 = False) 0
pld-class Phospholipidosis risk class (1 = positive, 0 = negative) 0 High 1

Approvals:

DateAgencyCompanyOrphan
None FDA LILLY

FDA Adverse Event Reporting System (Female)

None

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
Infective pulmonary exacerbation of cystic fibrosis 56.43 40.98 12 295 14759 110574233
Rubber sensitivity 48.78 40.98 8 299 2410 110586582
Pulmonary function test decreased 44.44 40.98 9 298 8691 110580301
Rhonchi 43.78 40.98 8 299 4510 110584482
Product administered at inappropriate site 42.37 40.98 8 299 5385 110583607

FDA Adverse Event Reporting System (Pediatric)

None

Pharmacologic Action:

SourceCodeDescription
ATC B02BA02 BLOOD AND BLOOD FORMING ORGANS
ANTIHEMORRHAGICS
VITAMIN K AND OTHER HEMOSTATICS
Vitamin K
CHEBI has role CHEBI:76971 <em>Escherichia coli</em> metabolite
CHEBI has role CHEBI:35610 antineoplastic agent
CHEBI has role CHEBI:48422 angiogenesis inhibitor
CHEBI has role CHEBI:50733 nutraceutical
CHEBI has role CHEBI:84087 human urinary metabolite
CHEBI has role CHEBI:147285 EC 3.4.22.69 (SARS coronavirus main proteinase) inhibitor

Related Drugs by ATC class:

B02BA Vitamin K 1 drug

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

None




🐶 Veterinary Drug Use

None

🐶 Veterinary products

None

Acid dissociation constants calculated using MoKa v3.0.0

None

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
Aldehyde oxidase Enzyme IC50 4 CHEMBL
Glutathione reductase, mitochondrial Enzyme Ki 4.92 CHEMBL
Amine oxidase [flavin-containing] B Enzyme Ki 6.40 CHEMBL
Amine oxidase [flavin-containing] A Enzyme Ki 4.59 CHEMBL
Indoleamine 2,3-dioxygenase 1 Enzyme IC50 6 CHEMBL
M-phase inducer phosphatase 2 Enzyme IC50 5.66 CHEMBL
Dual specificity phosphatase Cdc25C Enzyme IC50 4.73 CHEMBL
Ubiquitin carboxyl-terminal hydrolase isozyme L3 Enzyme IC50 4.15 CHEMBL
Dual specificity phosphatase Cdc25A Enzyme IC50 5.16 CHEMBL
Alpha-synuclein Transporter IC50 4.82 CHEMBL
Trypanothione reductase Enzyme IC50 4.26 CHEMBL
Dual specificity protein phosphatase 6 Enzyme IC50 4.69 CHEMBL
Dual specificity protein phosphatase 1 Enzyme IC50 4.62 CHEMBL
Replicase polyprotein 1ab Enzyme IC50 5.43 CHEMBL

External reference:

IDSource
4019127 VUID
N0000147378 NUI
D02335 KEGG_DRUG
1182-68-9 SECONDARY_CAS_RN
4019127 VANDF
C0025270 UMLSCUI
CHEBI:28869 CHEBI
VK3 PDB_CHEM_ID
CHEMBL590 ChEMBL_ID
DB00170 DRUGBANK_ID
CHEMBL4297659 ChEMBL_ID
4055 PUBCHEM_CID
723JX6CXY5 UNII
DB15381 DRUGBANK_ID
42781 RXNORM
337527 MMSL
35482 MMSL
NOCODE MMSL
d09345 MMSL
001039 NDDF
012756 NDDF
22606007 SNOMEDCT_US
412244007 SNOMEDCT_US
69576000 SNOMEDCT_US

Pharmaceutical products:

None