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

Stem definitionDrug idCAS RN
3855 112-85-6

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • docosanoic acid
  • behenic acid
  • hydrofol
  • Molecular weight: 340.59
  • Formula: C22H44O2
  • CLOGP: 10.39
  • LIPINSKI: 1
  • HAC: 2
  • HDO: 1
  • TPSA: 37.30
  • ALOGS: -7.05
  • ROTB: 20

Drug dosage:

None

ADMET properties:

None

Predicted pharmacokinetic/toxicological properties (PK-AZ):

PropertyDescriptionValueUnitConfidenceSimilarity
azlogd74 LogD at pH 7.4 6.056 Moderate 0.71
caco2-efflux Caco-2 efflux ratio (BA/AB) 10.023 Moderate 0.71
caco2-intrinsic-papp Caco-2 intrinsic apparent permeability 0 10^-6 cm/s Moderate 0.71
dh-clint Dog hepatocyte intrinsic clearance 1428.894 uL/min/10^6 cells Moderate 0.71
dppb Dog plasma protein binding (% unbound) 0 % Moderate 0.71
fcs-ppb Fetal calf serum protein binding (% unbound) 0 % Moderate 0.71
herg hERG pIC50 4.143 pIC50 Moderate 0.71
hh-clint Human hepatocyte intrinsic clearance 2355.049 uL/min/10^6 cells Moderate 0.71
hlm-clint Human liver microsomal intrinsic clearance 13.740 uL/min/mg protein Moderate 0.71
hppb Human plasma protein binding (% unbound) 0.070 % Moderate 0.71
kinase-safety-class ACVR2A,ACVR2B,ACVRL1,AKT3,ALK,AURKA,AXL,BRAF,BTK,CAMK2B,CAMK2D,CDK4,CDK5,CDK9,DDR1,DYRK1B,EGFR,EIF2AK3,EPHB4,ERBB2,FLT3,GRK2,GSK3B,IKBKB,ITK,JAK1,JAK2,JAK3,MAP2K6,MAP3K21,MAP3K7,MAPK10,MAPK7,MAPK9,MAPKAPK2,MTOR,NTRK2,PDK1,PDK2,PDK4,PDPK1,PIK3CA,PIK3CB,PIK3CD,PIK3CG,PIM2,PLK1,PRKCD,PRKDC,SIK2,SIK3,STK33,SYK,TEK,TGFBR1,TTK,ULK1,ZAP70 58
kinase-selectivity-class AKT2,AXL,CAMK2A,CAMK2D,CDK4,CSNK2A2,EIF2AK3,EPHB4,FLT4,GRK2,INSR,MAP2K6,MAPK10,MAPK7,MAPK8,MTOR,PDK4,PLK1,PLK2,PLK3,PLK4,PRKCD,PTK2,SIK2,STK33,TEK,TTK,ZAP70 28
mdck-mdr1-efflux MDCK-MDR1 efflux ratio 0.292 Moderate 0.71
mh-clint Mouse hepatocyte intrinsic clearance 107.895 Moderate 0.71
mppb Mouse plasma protein binding (% unbound) 0.010 Moderate 0.71
nih-mdck-mdr1-efflux NIH MDCK-MDR1 efflux ratio 0.005 Moderate 0.71
pfas-class PFAS structural alert (1 = True, 0 = False) 0
pppb Pig plasma protein binding (% unbound) 0 % Moderate 0.71
rh-clint Rat hepatocyte intrinsic clearance 65.013 uL/min/10^6 cells Moderate 0.71
rh-fuinc Rat hepatocyte fraction unbound in incubation 0 % Moderate 0.71
rppb Rat plasma protein binding (% unbound) 0.020 % Moderate 0.71
solubility-dd Solubility at pH 7.4 in DMSO 0.252 uM Moderate 0.71

Approvals:

None

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
CHEBI has role CHEBI:76924 plant metabolite

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 4.76 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
Peroxisome proliferator-activated receptor alpha Nuclear hormone receptor IC50 4.52 CHEMBL
Peroxisome proliferator-activated receptor gamma Nuclear hormone receptor IC50 4.52 CHEMBL
Peroxisome proliferator-activated receptor delta Nuclear hormone receptor IC50 4.52 CHEMBL

External reference:

IDSource
CHEBI:28941 CHEBI
EO3 PDB_CHEM_ID
CHEMBL1173474 ChEMBL_ID
1368203 RXNORM
013590 NDDF
C0053073 UMLSCUI
8215 PUBCHEM_CID
C007547 MESH_SUPPLEMENTAL_RECORD_UI
H390488X0A UNII

Pharmaceutical products:

None