Itaconic acid

Details

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Internal ID 3939c737-4a77-455c-b458-1b0248e0c3df
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Branched fatty acids
IUPAC Name 2-methylidenebutanedioic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H6O4/c1-3(5(8)9)2-4(6)7/h1-2H2,(H,6,7)(H,8,9)
InChI Key LVHBHZANLOWSRM-UHFFFAOYSA-N
Popularity 3,232 references in papers

Physical and Chemical Properties

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Molecular Formula C5H6O4
Molecular Weight 130.10 g/mol
Exact Mass 130.02660867 g/mol
Topological Polar Surface Area (TPSA) 74.60 Ų
XlogP -0.10
Atomic LogP (AlogP) 0.10
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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97-65-4
2-Methylenesuccinic acid
METHYLENESUCCINIC ACID
2-methylidenebutanedioic acid
Methylenebutanedioic acid
Propylenedicarboxylic acid
Butanedioic acid, methylene-
itaconate
2-Propene-1,2-dicarboxylic acid
Succinic acid, methylene-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Itaconic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8909 89.09%
Caco-2 - 0.7093 70.93%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.7410 74.10%
OATP2B1 inhibitior - 0.8603 86.03%
OATP1B1 inhibitior + 0.9612 96.12%
OATP1B3 inhibitior + 0.9468 94.68%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9833 98.33%
P-glycoprotein inhibitior - 0.9805 98.05%
P-glycoprotein substrate - 0.9850 98.50%
CYP3A4 substrate - 0.7751 77.51%
CYP2C9 substrate - 0.5963 59.63%
CYP2D6 substrate - 0.8730 87.30%
CYP3A4 inhibition - 0.9101 91.01%
CYP2C9 inhibition - 0.9418 94.18%
CYP2C19 inhibition - 0.9587 95.87%
CYP2D6 inhibition - 0.9438 94.38%
CYP1A2 inhibition - 0.9542 95.42%
CYP2C8 inhibition - 0.9887 98.87%
CYP inhibitory promiscuity - 0.9814 98.14%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5635 56.35%
Carcinogenicity (trinary) Non-required 0.7196 71.96%
Eye corrosion + 0.8586 85.86%
Eye irritation + 0.9850 98.50%
Skin irritation + 0.6026 60.26%
Skin corrosion + 0.5812 58.12%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8173 81.73%
Micronuclear - 0.7700 77.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation + 0.6446 64.46%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.5917 59.17%
Acute Oral Toxicity (c) III 0.6416 64.16%
Estrogen receptor binding - 0.9067 90.67%
Androgen receptor binding - 0.9087 90.87%
Thyroid receptor binding - 0.8676 86.76%
Glucocorticoid receptor binding - 0.8678 86.78%
Aromatase binding - 0.8723 87.23%
PPAR gamma - 0.6366 63.66%
Honey bee toxicity - 0.9554 95.54%
Biodegradation + 0.9250 92.50%
Crustacea aquatic toxicity - 0.9100 91.00%
Fish aquatic toxicity + 0.8791 87.91%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4040 P28482 MAP kinase ERK2 92.27% 83.82%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.46% 99.17%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 81.27% 81.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.97% 96.09%
CHEMBL1255126 O15151 Protein Mdm4 80.36% 90.20%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.32% 91.11%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Lilium longiflorum
Lotus corniculatus subsp. corniculatus
Medicago sativa
Pycnandra acuminata

Cross-Links

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PubChem 811
LOTUS LTS0092941
wikiData Q903311