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

Stem definitionDrug idCAS RN
4612 139-85-5

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • protocatechualdehyde
  • catechaldehyde
  • protocatechuic aldehyde
found in wheat grains, wheat seedlings, & other plants; RN given refers to parent cpd; see also rancinamycins; structure
  • Molecular weight: 138.12
  • Formula: C7H6O3
  • CLOGP: 1.03
  • LIPINSKI: 0
  • HAC: 3
  • HDO: 2
  • TPSA: 57.53
  • ALOGS: -0.99
  • ROTB: 1

Drug dosage:

None

ADMET properties:

None

Predicted pharmacokinetic/toxicological properties (PK-AZ):

PropertyDescriptionValueUnitConfidenceSimilarity
kinase-safety-class ACVR2A,ACVR2B,ACVRL1,AKT2,AKT3,ALK,AURKA,AURKB,AURKC,AXL,BMX,BRAF,BTK,CAMK2B,CAMK2D,CDK1,CDK19,CDK2,CDK4,CDK5,CDK9,CSF1R,DDR1,DYRK1B,EGFR,EIF2AK3,EPHA2,EPHB4,ERBB2,FGFR1,FLT1,FLT3,FLT4,GRK2,GRK3,GSK3A,GSK3B,IGF1R,IRAK1,ITK,JAK1,JAK2,JAK3,KDR,KIT,MAP2K6,MAP3K1,MAP3K10,MAP3K14,MAP3K2,MAP3K21,MAP3K3,MAP3K7,MAP4K1,MAP4K3,MAP4K5,MAPK1,MAPK10,MAPK12,MAPK14,MAPK7,MAPK8,MAPK9,MAPKAPK2,MARK4,MELK,MET,MTOR,NTRK1,NTRK2,PAK4,PDK1,PDK2,PDK4,PDPK1,PIK3CA,PIK3CB,PIK3CD,PIM1,PIM2,PLK1,PRKCD,PRKDC,PTK2,SGK1,SIK2,SIK3,SRC,STK10,STK33,SYK,TEK,TGFBR1,TTK,ULK1,ULK2,ZAP70 97
kinase-selectivity-class ACVR2A,ACVR2B,ACVRL1,AURKB,AXL,BMX,BRAF,CAMK2B,CAMK2D,CDK4,CDK9,DDR1,DYRK1B,EIF2AK3,EPHB4,ERBB2,FGFR1,GRK2,GSK3B,IRAK1,JAK2,KIT,MAP2K3,MAP2K6,MAP3K14,MAPK1,MAPK7,MAPK8,MARK4,PIK3CB,PIK3CD,PRKDC,SIK2,STK33,SYK,TEK,TGFBR1,TTK,ULK1 39
pfas-class PFAS structural alert (1 = True, 0 = False) 0

Approvals:

DateAgencyCompanyOrphan
None FDA

FDA Adverse Event Reporting System (Female)

None

FDA Adverse Event Reporting System (Male)

None

FDA Adverse Event Reporting System (Geriatric)

None

FDA Adverse Event Reporting System (Pediatric)

None

Pharmacologic Action:

SourceCodeDescription
MeSH PA D000925 Anticoagulants
MeSH PA D006401 Hematologic Agents

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

Dissociation levelDissociation constantType (acidic/basic)
pKa1 7.16 acidic
pKa2 11.57 acidic

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
Prostaglandin G/H synthase 2 Enzyme IC50 4.71 CHEMBL

External reference:

IDSource
CHEBI:50205 CHEBI
H6N PDB_CHEM_ID
CHEMBL222021 ChEMBL_ID
C005581 MESH_SUPPLEMENTAL_RECORD_UI
DB11268 DRUGBANK_ID
4PVP2HCH4T UNII
1362689 RXNORM
C0072487 UMLSCUI
8768 PUBCHEM_CID

Pharmaceutical products:

ProductCategoryIngredientsNDCFormQuantityRouteMarketingLabel
O HUI WHITE EXTREME CELLIGHT HUMAN OTC DRUG LABEL 1 53208-501 EMULSION 0.03 mL TOPICAL unapproved drug other 9 sections
O HUI WHITE EXTREME CELLIGHT HUMAN OTC DRUG LABEL 1 53208-507 CREAM 0.03 mL TOPICAL unapproved drug other 9 sections