5-Methyl-hept-3-en-2-one

Details

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Internal ID 1ba99c7a-e92d-4233-8b68-990501d0d988
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha,beta-unsaturated ketones > Enones
IUPAC Name 5-methylhept-3-en-2-one
SMILES (Canonical) CCC(C)C=CC(=O)C
SMILES (Isomeric) CCC(C)C=CC(=O)C
InChI InChI=1S/C8H14O/c1-4-7(2)5-6-8(3)9/h5-7H,4H2,1-3H3
InChI Key QDUQNQQMHZNNTG-UHFFFAOYSA-N
Popularity 0 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 2.10
Atomic LogP (AlogP) 2.18
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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QDUQNQQMHZNNTG-UHFFFAOYSA-N

2D Structure

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2D Structure of 5-Methyl-hept-3-en-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 + 0.9949 99.49%
Caco-2 + 0.8787 87.87%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.3676 36.76%
OATP2B1 inhibitior - 0.8634 86.34%
OATP1B1 inhibitior + 0.9096 90.96%
OATP1B3 inhibitior + 0.9542 95.42%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8416 84.16%
P-glycoprotein inhibitior - 0.9746 97.46%
P-glycoprotein substrate - 0.9674 96.74%
CYP3A4 substrate - 0.7129 71.29%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8733 87.33%
CYP3A4 inhibition - 0.9670 96.70%
CYP2C9 inhibition - 0.9335 93.35%
CYP2C19 inhibition - 0.9147 91.47%
CYP2D6 inhibition - 0.9380 93.80%
CYP1A2 inhibition - 0.6400 64.00%
CYP2C8 inhibition - 0.9891 98.91%
CYP inhibitory promiscuity - 0.7105 71.05%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.5274 52.74%
Eye corrosion + 0.9676 96.76%
Eye irritation + 0.9265 92.65%
Skin irritation + 0.8264 82.64%
Skin corrosion - 0.8565 85.65%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6766 67.66%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.5500 55.00%
skin sensitisation + 0.9564 95.64%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.8333 83.33%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.5679 56.79%
Acute Oral Toxicity (c) III 0.8499 84.99%
Estrogen receptor binding - 0.9639 96.39%
Androgen receptor binding - 0.9061 90.61%
Thyroid receptor binding - 0.8924 89.24%
Glucocorticoid receptor binding - 0.9357 93.57%
Aromatase binding - 0.9284 92.84%
PPAR gamma - 0.9648 96.48%
Honey bee toxicity - 0.8921 89.21%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity - 0.9100 91.00%
Fish aquatic toxicity + 0.6646 66.46%

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 92.22% 96.09%
CHEMBL2581 P07339 Cathepsin D 89.40% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.86% 89.34%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.85% 100.00%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 82.83% 98.75%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.72% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.47% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.22% 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.
Salvia caespitosa

Cross-Links

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PubChem 138412
LOTUS LTS0037803
wikiData Q105218984