AromaDb: A Database of Plant's Aroma Molecules

1,4-Butanedicarboxylic acid Details

: IUPAC Name
Adipicacid
:Chemical Class
Acid
:CAS Registry Number
124-04-9
:Description

:Fragrance Type
soure

Physical and Chemical properties

PUBCHEM ID 196
Molecular Weight (g/mol) 146.146
Molecular Formula C6H10O4
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 3
IUPAC Name Adipicacid
Canonical SMILES O=C(O)CCCCC(=O)O
PUBCHEM IUPAC INCHIKEY WNLRTRBMVRJNCN-UHFFFAOYSA-N
Solubility Level 5
Vapour Pressure -5.886

Absorption and Metabolism information

XLOGP3 AA NA
CACTVS TPSA 37.29
BBB Level 3
Absorption Level 0
EXT PPB#Prediction 0
AlogP98 0.553
EXT CYP2D6#Prediction 0

Toxicological Information

Mouse Female FDA Non-Carcinogen
Mouse Male FDA Multi-Carcinogen
Rat Female FDA Single-Carcinogen
Rat Male FDA Multi-Carcinogen
Ames Prediction Non-Mutagen
Developmental / Reproductive Toxicity Non-Toxic
Rat Oral LD50 3.61844
Ocular Irritancy None
Hepatotoxic#Prediction 0
Effected Human Genes NA

Ecological Information

Aerobic Biodegradability Prediction Degradable

Hazard(s) Identification

Physical hazards not classified
Health hazards None
Environmental hazards not classified
About Table Headings

Compound Biological Activity

Serial No.Cas No Gene SymbolOrganismInteractionInteraction Actions PubMed Id
1124-04-9SLC22A6Homo sapiensadipic acid inhibits the reaction [SLC22A6 protein results in increased susceptibility to [mercuric oxide co-treated with Acetylcysteine]] affects^cotreatment|decreases^reaction|increases^response to substance 12606766
2124-04-9SLC22A6Homo sapiensadipic acid inhibits the reaction [SLC22A6 protein results in increased susceptibility to [mercuric oxide co-treated with Acetylcysteine]] affects^cotreatment|decreases^reaction|increases^response to substance 12606766
Serial No. Activity Name DetailsReferences (PubMed)Other details EPA (U.S) Clinical Trials (U.S. NIH)
1 124-04-9 1,4-Butanedicarboxylic acid

Compound Image


2D Structure

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