2-(2-Methylbut-2-enoyloxymethyl)but-2-enoic acid

Details

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Internal ID 0e79a6db-ce75-4b59-ae40-a2b2329e7db8
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name 2-(2-methylbut-2-enoyloxymethyl)but-2-enoic acid
SMILES (Canonical) CC=C(C)C(=O)OCC(=CC)C(=O)O
SMILES (Isomeric) CC=C(C)C(=O)OCC(=CC)C(=O)O
InChI InChI=1S/C10H14O4/c1-4-7(3)10(13)14-6-8(5-2)9(11)12/h4-5H,6H2,1-3H3,(H,11,12)
InChI Key MQFYOYGIGPVWSJ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H14O4
Molecular Weight 198.22 g/mol
Exact Mass 198.08920892 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.53
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(2-Methylbut-2-enoyloxymethyl)but-2-enoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9764 97.64%
Caco-2 + 0.5974 59.74%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7433 74.33%
OATP2B1 inhibitior - 0.8623 86.23%
OATP1B1 inhibitior + 0.9295 92.95%
OATP1B3 inhibitior + 0.9381 93.81%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8133 81.33%
P-glycoprotein inhibitior - 0.9852 98.52%
P-glycoprotein substrate - 0.9756 97.56%
CYP3A4 substrate - 0.6393 63.93%
CYP2C9 substrate + 0.6153 61.53%
CYP2D6 substrate - 0.9262 92.62%
CYP3A4 inhibition - 0.8794 87.94%
CYP2C9 inhibition - 0.8532 85.32%
CYP2C19 inhibition - 0.8937 89.37%
CYP2D6 inhibition - 0.9133 91.33%
CYP1A2 inhibition - 0.9026 90.26%
CYP2C8 inhibition - 0.9657 96.57%
CYP inhibitory promiscuity - 0.9052 90.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5649 56.49%
Carcinogenicity (trinary) Non-required 0.6786 67.86%
Eye corrosion - 0.7446 74.46%
Eye irritation + 0.7705 77.05%
Skin irritation + 0.6598 65.98%
Skin corrosion - 0.8130 81.30%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6927 69.27%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation - 0.5887 58.87%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.7923 79.23%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.7590 75.90%
Acute Oral Toxicity (c) III 0.5046 50.46%
Estrogen receptor binding - 0.8425 84.25%
Androgen receptor binding - 0.7867 78.67%
Thyroid receptor binding - 0.8605 86.05%
Glucocorticoid receptor binding - 0.7723 77.23%
Aromatase binding - 0.5897 58.97%
PPAR gamma - 0.9086 90.86%
Honey bee toxicity - 0.8908 89.08%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.7655 76.55%
Fish aquatic toxicity + 0.9588 95.88%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.82% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.78% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.70% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 83.15% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.16% 86.33%

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.
Anthriscus sylvestris

Cross-Links

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PubChem 155257
LOTUS LTS0212478
wikiData Q105169979