Citraconic anhydride

Details

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Internal ID 9315b362-f7ad-454a-9922-5ea26f85a440
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name 3-methylfuran-2,5-dione
SMILES (Canonical) CC1=CC(=O)OC1=O
SMILES (Isomeric) CC1=CC(=O)OC1=O
InChI InChI=1S/C5H4O3/c1-3-2-4(6)8-5(3)7/h2H,1H3
InChI Key AYKYXWQEBUNJCN-UHFFFAOYSA-N
Popularity 499 references in papers

Physical and Chemical Properties

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Molecular Formula C5H4O3
Molecular Weight 112.08 g/mol
Exact Mass 112.016043985 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 0.20
Atomic LogP (AlogP) 0.02
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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616-02-4
3-methylfuran-2,5-dione
2,5-Furandione, 3-methyl-
2-Methylmaleic anhydride
METHYLMALEIC ANHYDRIDE
3-Methylmaleic anhydride
Citraconic acid anhydride
Monomethylmaleic anhydride
Maleic anhydride, methyl-
3-methyl-2,5-dihydrofuran-2,5-dione
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Citraconic anhydride

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9944 99.44%
Caco-2 + 0.5106 51.06%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.6914 69.14%
OATP2B1 inhibitior - 0.8727 87.27%
OATP1B1 inhibitior + 0.9292 92.92%
OATP1B3 inhibitior + 0.9705 97.05%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9356 93.56%
P-glycoprotein inhibitior - 0.9852 98.52%
P-glycoprotein substrate - 0.9911 99.11%
CYP3A4 substrate - 0.6950 69.50%
CYP2C9 substrate + 0.5989 59.89%
CYP2D6 substrate - 0.9042 90.42%
CYP3A4 inhibition - 0.9785 97.85%
CYP2C9 inhibition - 0.9074 90.74%
CYP2C19 inhibition - 0.8195 81.95%
CYP2D6 inhibition - 0.9593 95.93%
CYP1A2 inhibition - 0.6915 69.15%
CYP2C8 inhibition - 0.9919 99.19%
CYP inhibitory promiscuity - 0.8178 81.78%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8271 82.71%
Carcinogenicity (trinary) Non-required 0.4588 45.88%
Eye corrosion + 0.8970 89.70%
Eye irritation + 0.9913 99.13%
Skin irritation + 0.7508 75.08%
Skin corrosion + 0.8392 83.92%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7989 79.89%
Micronuclear + 0.5400 54.00%
Hepatotoxicity + 0.7302 73.02%
skin sensitisation - 0.6014 60.14%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.7752 77.52%
Acute Oral Toxicity (c) III 0.7988 79.88%
Estrogen receptor binding - 0.9570 95.70%
Androgen receptor binding - 0.8469 84.69%
Thyroid receptor binding - 0.8826 88.26%
Glucocorticoid receptor binding - 0.9091 90.91%
Aromatase binding - 0.8863 88.63%
PPAR gamma - 0.9182 91.82%
Honey bee toxicity - 0.9691 96.91%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9211 92.11%

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
CHEMBL2581 P07339 Cathepsin D 92.73% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.42% 95.56%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 84.85% 93.65%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.45% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 83.43% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.31% 94.00%

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.
Coffea arabica
Schisandra chinensis

Cross-Links

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PubChem 12012
NPASS NPC42513
LOTUS LTS0258552
wikiData Q26840748