5-Isopropyl-3-hepten-2-one

Details

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Internal ID 6ef71950-5f7d-4817-90d9-08759c3569b7
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha,beta-unsaturated ketones > Enones
IUPAC Name 5-ethyl-6-methylhept-3-en-2-one
SMILES (Canonical) CCC(C=CC(=O)C)C(C)C
SMILES (Isomeric) CCC(C=CC(=O)C)C(C)C
InChI InChI=1S/C10H18O/c1-5-10(8(2)3)7-6-9(4)11/h6-8,10H,5H2,1-4H3
InChI Key BCYUENXUQILNAA-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H18O
Molecular Weight 154.25 g/mol
Exact Mass 154.135765193 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.81
H-Bond Acceptor 1
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 5-Isopropyl-3-hepten-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 + 0.9969 99.69%
Caco-2 + 0.8042 80.42%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.4648 46.48%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9359 93.59%
OATP1B3 inhibitior + 0.9537 95.37%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9131 91.31%
P-glycoprotein inhibitior - 0.9749 97.49%
P-glycoprotein substrate - 0.9399 93.99%
CYP3A4 substrate - 0.6977 69.77%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8733 87.33%
CYP3A4 inhibition - 0.9789 97.89%
CYP2C9 inhibition - 0.9072 90.72%
CYP2C19 inhibition - 0.9031 90.31%
CYP2D6 inhibition - 0.9463 94.63%
CYP1A2 inhibition - 0.6403 64.03%
CYP2C8 inhibition - 0.9891 98.91%
CYP inhibitory promiscuity - 0.7021 70.21%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5700 57.00%
Carcinogenicity (trinary) Non-required 0.6415 64.15%
Eye corrosion + 0.9660 96.60%
Eye irritation + 0.9566 95.66%
Skin irritation + 0.8947 89.47%
Skin corrosion - 0.6992 69.92%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5558 55.58%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5553 55.53%
skin sensitisation + 0.9515 95.15%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity + 0.5693 56.93%
Acute Oral Toxicity (c) III 0.8189 81.89%
Estrogen receptor binding - 0.9572 95.72%
Androgen receptor binding - 0.9376 93.76%
Thyroid receptor binding - 0.8691 86.91%
Glucocorticoid receptor binding - 0.9136 91.36%
Aromatase binding - 0.9251 92.51%
PPAR gamma - 0.9702 97.02%
Honey bee toxicity - 0.9354 93.54%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.9100 91.00%
Fish aquatic toxicity + 0.7342 73.42%

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 92.86% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.62% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.15% 85.14%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 85.71% 97.21%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.50% 89.34%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.04% 97.25%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 83.41% 100.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.69% 96.95%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 81.68% 98.75%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.33% 93.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.08% 99.17%

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.
Nicotiana tabacum

Cross-Links

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PubChem 538599
LOTUS LTS0028274
wikiData Q104923717