5-Methyl-3-hexen-2-one

Details

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Internal ID fe0a34eb-9665-4753-a0d1-fa4cd6cb2f34
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha,beta-unsaturated ketones > Enones
IUPAC Name (E)-5-methylhex-3-en-2-one
SMILES (Canonical) CC(C)C=CC(=O)C
SMILES (Isomeric) CC(C)/C=C/C(=O)C
InChI InChI=1S/C7H12O/c1-6(2)4-5-7(3)8/h4-6H,1-3H3/b5-4+
InChI Key IYMKNYVCXUEFJE-SNAWJCMRSA-N
Popularity 36 references in papers

Physical and Chemical Properties

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Molecular Formula C7H12O
Molecular Weight 112.17 g/mol
Exact Mass 112.088815002 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.79
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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3-Hexen-2-one, 5-methyl-
5166-53-0
(E)-5-methylhex-3-en-2-one
2-Oxo-5-methylhex-3-ene
5-Methyl-3E-hexen-2-one
FEMA No. 3409
1821-29-0
(3E)-5-methylhex-3-en-2-one
8L0NZD2EIQ
(E)-5-Methyl-3-hexen-2-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 5-Methyl-3-hexen-2-one

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 + 0.6317 63.17%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5427 54.27%
OATP2B1 inhibitior - 0.8695 86.95%
OATP1B1 inhibitior + 0.9589 95.89%
OATP1B3 inhibitior + 0.9645 96.45%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8885 88.85%
P-glycoprotein inhibitior - 0.9709 97.09%
P-glycoprotein substrate - 0.9861 98.61%
CYP3A4 substrate - 0.7407 74.07%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8847 88.47%
CYP3A4 inhibition - 0.9668 96.68%
CYP2C9 inhibition - 0.9364 93.64%
CYP2C19 inhibition - 0.9193 91.93%
CYP2D6 inhibition - 0.9595 95.95%
CYP1A2 inhibition - 0.7839 78.39%
CYP2C8 inhibition - 0.9959 99.59%
CYP inhibitory promiscuity - 0.8123 81.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5983 59.83%
Carcinogenicity (trinary) Non-required 0.6008 60.08%
Eye corrosion + 0.9919 99.19%
Eye irritation + 0.9855 98.55%
Skin irritation + 0.8473 84.73%
Skin corrosion - 0.7073 70.73%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7889 78.89%
Micronuclear - 0.7100 71.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation + 0.8371 83.71%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.6498 64.98%
Acute Oral Toxicity (c) III 0.8594 85.94%
Estrogen receptor binding - 0.9735 97.35%
Androgen receptor binding - 0.9294 92.94%
Thyroid receptor binding - 0.9099 90.99%
Glucocorticoid receptor binding - 0.9305 93.05%
Aromatase binding - 0.9184 91.84%
PPAR gamma - 0.9394 93.94%
Honey bee toxicity - 0.9023 90.23%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.9200 92.00%
Fish aquatic toxicity - 0.5217 52.17%

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 87.50% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.30% 85.14%
CHEMBL2581 P07339 Cathepsin D 80.62% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.05% 94.45%

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.
Cryptomeria japonica
Isodon lophanthoides
Salvia deserta

Cross-Links

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PubChem 5363140
LOTUS LTS0074488
wikiData Q105287348