2-Methyl-2-hepten-4-one

Details

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Internal ID 19e4802c-cd70-4af3-a1e8-124ea5c5a64e
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha,beta-unsaturated ketones > Enones
IUPAC Name 2-methylhept-2-en-4-one
SMILES (Canonical) CCCC(=O)C=C(C)C
SMILES (Isomeric) CCCC(=O)C=C(C)C
InChI InChI=1S/C8H14O/c1-4-5-8(9)6-7(2)3/h6H,4-5H2,1-3H3
InChI Key FKMGZMDLSNOJPQ-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C8H14O
Molecular Weight 126.20 g/mol
Exact Mass 126.104465066 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.32
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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2-methylhept-2-en-4-one
22319-24-0
2-Hepten-4-one, 2-methyl-
2-methyl-hept-2-en-4-one
SCHEMBL4391467
DTXSID30176863
AKOS017730460

2D Structure

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2D Structure of 2-Methyl-2-hepten-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 + 0.9717 97.17%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Nucleus 0.4545 45.45%
OATP2B1 inhibitior - 0.8524 85.24%
OATP1B1 inhibitior + 0.9247 92.47%
OATP1B3 inhibitior + 0.9470 94.70%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8799 87.99%
P-glycoprotein inhibitior - 0.9869 98.69%
P-glycoprotein substrate - 0.9532 95.32%
CYP3A4 substrate - 0.7118 71.18%
CYP2C9 substrate - 0.8058 80.58%
CYP2D6 substrate - 0.8550 85.50%
CYP3A4 inhibition - 0.9502 95.02%
CYP2C9 inhibition - 0.9092 90.92%
CYP2C19 inhibition - 0.8882 88.82%
CYP2D6 inhibition - 0.9406 94.06%
CYP1A2 inhibition - 0.5795 57.95%
CYP2C8 inhibition - 0.9793 97.93%
CYP inhibitory promiscuity - 0.6080 60.80%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5400 54.00%
Carcinogenicity (trinary) Non-required 0.4953 49.53%
Eye corrosion + 0.7059 70.59%
Eye irritation + 0.9913 99.13%
Skin irritation + 0.7692 76.92%
Skin corrosion - 0.9564 95.64%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7697 76.97%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5448 54.48%
skin sensitisation + 0.9444 94.44%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.9500 95.00%
Nephrotoxicity - 0.5860 58.60%
Acute Oral Toxicity (c) III 0.8022 80.22%
Estrogen receptor binding - 0.9850 98.50%
Androgen receptor binding - 0.8827 88.27%
Thyroid receptor binding - 0.9074 90.74%
Glucocorticoid receptor binding - 0.8760 87.60%
Aromatase binding - 0.9252 92.52%
PPAR gamma - 0.8813 88.13%
Honey bee toxicity - 0.9582 95.82%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.8000 80.00%
Fish aquatic toxicity - 0.4324 43.24%

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 91.38% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.99% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.80% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.79% 94.45%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.73% 96.95%
CHEMBL221 P23219 Cyclooxygenase-1 80.15% 90.17%

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.
Aspalathus linearis
Curcuma longa

Cross-Links

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PubChem 31138
NPASS NPC303866
LOTUS LTS0179778
wikiData Q83047192