Methyl vinyl ketone

Details

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Internal ID 3b3aef9d-0767-496c-8cf1-1ad351ceb9fb
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha,beta-unsaturated ketones > Enones
IUPAC Name but-3-en-2-one
SMILES (Canonical) CC(=O)C=C
SMILES (Isomeric) CC(=O)C=C
InChI InChI=1S/C4H6O/c1-3-4(2)5/h3H,1H2,2H3
InChI Key FUSUHKVFWTUUBE-UHFFFAOYSA-N
Popularity 2,264 references in papers

Physical and Chemical Properties

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Molecular Formula C4H6O
Molecular Weight 70.09 g/mol
Exact Mass 70.041864811 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 0.50
Atomic LogP (AlogP) 0.76
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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3-Buten-2-one
but-3-en-2-one
78-94-4
Butenone
Vinyl methyl ketone
Methylene acetone
2-Butenone
Methylvinylketon
Acetyl ethylene
1-Buten-3-one
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Methyl vinyl ketone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9937 99.37%
Caco-2 + 0.8388 83.88%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.4680 46.80%
OATP2B1 inhibitior - 0.8746 87.46%
OATP1B1 inhibitior + 0.9645 96.45%
OATP1B3 inhibitior + 0.9642 96.42%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9201 92.01%
P-glycoprotein inhibitior - 0.9855 98.55%
P-glycoprotein substrate - 0.9961 99.61%
CYP3A4 substrate - 0.7671 76.71%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8388 83.88%
CYP3A4 inhibition - 0.9574 95.74%
CYP2C9 inhibition - 0.9523 95.23%
CYP2C19 inhibition - 0.8823 88.23%
CYP2D6 inhibition - 0.9721 97.21%
CYP1A2 inhibition - 0.7695 76.95%
CYP2C8 inhibition - 0.9948 99.48%
CYP inhibitory promiscuity - 0.8574 85.74%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6983 69.83%
Carcinogenicity (trinary) Non-required 0.6484 64.84%
Eye corrosion + 0.9972 99.72%
Eye irritation + 0.9886 98.86%
Skin irritation + 0.8920 89.20%
Skin corrosion + 0.9671 96.71%
Ames mutagenesis + 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8254 82.54%
Micronuclear + 0.6100 61.00%
Hepatotoxicity + 0.8750 87.50%
skin sensitisation + 0.9272 92.72%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.7338 73.38%
Acute Oral Toxicity (c) I 0.7794 77.94%
Estrogen receptor binding - 0.9330 93.30%
Androgen receptor binding - 0.8917 89.17%
Thyroid receptor binding - 0.8935 89.35%
Glucocorticoid receptor binding - 0.8416 84.16%
Aromatase binding - 0.9120 91.20%
PPAR gamma - 0.8708 87.08%
Honey bee toxicity - 0.8509 85.09%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.9400 94.00%
Fish aquatic toxicity - 0.4457 44.57%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL3577 P00352 Aldehyde dehydrogenase 1A1 19952.6 nM
Potency
via CMAUP

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 87.07% 82.05%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.01% 96.09%
CHEMBL340 P08684 Cytochrome P450 3A4 81.71% 91.19%

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.
Artemisia argyi
Artemisia montana
Artemisia princeps
Zanthoxylum bungeanum
Zanthoxylum schinifolium

Cross-Links

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PubChem 6570
NPASS NPC94980
ChEMBL CHEMBL1600824