(2-Methylidene-3-oxobutyl) 2-methylprop-2-enoate

Details

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Internal ID 0b5a4ecf-0715-42e5-b9cf-333ca998d730
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha,beta-unsaturated ketones > Alpha-branched alpha,beta-unsaturated ketones
IUPAC Name (2-methylidene-3-oxobutyl) 2-methylprop-2-enoate
SMILES (Canonical) CC(=C)C(=O)OCC(=C)C(=O)C
SMILES (Isomeric) CC(=C)C(=O)OCC(=C)C(=O)C
InChI InChI=1S/C9H12O3/c1-6(2)9(11)12-5-7(3)8(4)10/h1,3,5H2,2,4H3
InChI Key MWZGBLCWNBDPCZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C9H12O3
Molecular Weight 168.19 g/mol
Exact Mass 168.078644241 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.25
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2-Methylidene-3-oxobutyl) 2-methylprop-2-enoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9903 99.03%
Caco-2 + 0.5989 59.89%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7971 79.71%
OATP2B1 inhibitior - 0.8592 85.92%
OATP1B1 inhibitior + 0.9674 96.74%
OATP1B3 inhibitior + 0.9500 95.00%
MATE1 inhibitior - 0.6800 68.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9130 91.30%
P-glycoprotein inhibitior - 0.9667 96.67%
P-glycoprotein substrate - 0.9460 94.60%
CYP3A4 substrate - 0.6061 60.61%
CYP2C9 substrate - 0.8012 80.12%
CYP2D6 substrate - 0.8922 89.22%
CYP3A4 inhibition - 0.8119 81.19%
CYP2C9 inhibition - 0.8485 84.85%
CYP2C19 inhibition - 0.7422 74.22%
CYP2D6 inhibition - 0.9225 92.25%
CYP1A2 inhibition - 0.7169 71.69%
CYP2C8 inhibition - 0.9703 97.03%
CYP inhibitory promiscuity - 0.6686 66.86%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5651 56.51%
Carcinogenicity (trinary) Non-required 0.6750 67.50%
Eye corrosion + 0.6399 63.99%
Eye irritation + 0.9653 96.53%
Skin irritation + 0.8565 85.65%
Skin corrosion - 0.8815 88.15%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7419 74.19%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation + 0.7292 72.92%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.7694 76.94%
Acute Oral Toxicity (c) II 0.6685 66.85%
Estrogen receptor binding - 0.8535 85.35%
Androgen receptor binding - 0.8355 83.55%
Thyroid receptor binding - 0.8025 80.25%
Glucocorticoid receptor binding - 0.8688 86.88%
Aromatase binding - 0.6620 66.20%
PPAR gamma - 0.8308 83.08%
Honey bee toxicity - 0.8661 86.61%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.8655 86.55%
Fish aquatic toxicity + 0.9642 96.42%

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 94.15% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 92.16% 83.82%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.48% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.48% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.02% 91.11%
CHEMBL2581 P07339 Cathepsin D 81.91% 98.95%

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.
Chamaemelum fuscatum

Cross-Links

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PubChem 85554070
LOTUS LTS0190964
wikiData Q105173903