3-(4-But-1-enyl-2,5-dioxofuran-3-yl)propanoic acid

Details

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Internal ID 8236cfee-0fb6-4a43-9b08-2f2be93d5cd6
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Tricarboxylic acids and derivatives
IUPAC Name 3-(4-but-1-enyl-2,5-dioxofuran-3-yl)propanoic acid
SMILES (Canonical) CCC=CC1=C(C(=O)OC1=O)CCC(=O)O
SMILES (Isomeric) CCC=CC1=C(C(=O)OC1=O)CCC(=O)O
InChI InChI=1S/C11H12O5/c1-2-3-4-7-8(5-6-9(12)13)11(15)16-10(7)14/h3-4H,2,5-6H2,1H3,(H,12,13)
InChI Key KMMGWWCKVLBXLF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H12O5
Molecular Weight 224.21 g/mol
Exact Mass 224.06847348 g/mol
Topological Polar Surface Area (TPSA) 80.70 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.20
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(4-But-1-enyl-2,5-dioxofuran-3-yl)propanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9793 97.93%
Caco-2 + 0.5848 58.48%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7574 75.74%
OATP2B1 inhibitior - 0.8578 85.78%
OATP1B1 inhibitior + 0.7971 79.71%
OATP1B3 inhibitior + 0.9585 95.85%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8070 80.70%
BSEP inhibitior - 0.9068 90.68%
P-glycoprotein inhibitior - 0.9770 97.70%
P-glycoprotein substrate - 0.9523 95.23%
CYP3A4 substrate - 0.6095 60.95%
CYP2C9 substrate + 0.6092 60.92%
CYP2D6 substrate - 0.8964 89.64%
CYP3A4 inhibition - 0.9487 94.87%
CYP2C9 inhibition - 0.9069 90.69%
CYP2C19 inhibition - 0.8700 87.00%
CYP2D6 inhibition - 0.9409 94.09%
CYP1A2 inhibition - 0.8789 87.89%
CYP2C8 inhibition - 0.8613 86.13%
CYP inhibitory promiscuity - 0.9559 95.59%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8825 88.25%
Carcinogenicity (trinary) Non-required 0.5751 57.51%
Eye corrosion - 0.8332 83.32%
Eye irritation + 0.9098 90.98%
Skin irritation + 0.5383 53.83%
Skin corrosion - 0.6771 67.71%
Ames mutagenesis - 0.8554 85.54%
Human Ether-a-go-go-Related Gene inhibition - 0.6630 66.30%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.6806 68.06%
skin sensitisation - 0.7921 79.21%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.5694 56.94%
Acute Oral Toxicity (c) III 0.7207 72.07%
Estrogen receptor binding - 0.8031 80.31%
Androgen receptor binding - 0.7923 79.23%
Thyroid receptor binding - 0.7546 75.46%
Glucocorticoid receptor binding - 0.6826 68.26%
Aromatase binding - 0.5625 56.25%
PPAR gamma + 0.5207 52.07%
Honey bee toxicity - 0.9774 97.74%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.7686 76.86%

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 96.36% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.29% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.88% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.84% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.07% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.39% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 82.69% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.36% 96.09%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 85144948
LOTUS LTS0004707
wikiData Q105143036