4,8-Dimethylnona-4,7-dien-2-one

Details

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Internal ID 564a548b-6f4c-460e-8c59-af5d44a83535
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name 4,8-dimethylnona-4,7-dien-2-one
SMILES (Canonical) CC(=CCC=C(C)CC(=O)C)C
SMILES (Isomeric) CC(=CCC=C(C)CC(=O)C)C
InChI InChI=1S/C11H18O/c1-9(2)6-5-7-10(3)8-11(4)12/h6-7H,5,8H2,1-4H3
InChI Key LLPHCJKTUJMQEQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H18O
Molecular Weight 166.26 g/mol
Exact Mass 166.135765193 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.27
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 4,8-Dimethylnona-4,7-dien-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 + 0.9941 99.41%
Caco-2 + 0.9351 93.51%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.4035 40.35%
OATP2B1 inhibitior - 0.8633 86.33%
OATP1B1 inhibitior + 0.9512 95.12%
OATP1B3 inhibitior + 0.9522 95.22%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8889 88.89%
P-glycoprotein inhibitior - 0.9759 97.59%
P-glycoprotein substrate - 0.9678 96.78%
CYP3A4 substrate - 0.7193 71.93%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7774 77.74%
CYP3A4 inhibition - 0.9340 93.40%
CYP2C9 inhibition - 0.9003 90.03%
CYP2C19 inhibition - 0.8513 85.13%
CYP2D6 inhibition - 0.9301 93.01%
CYP1A2 inhibition - 0.6595 65.95%
CYP2C8 inhibition - 0.9938 99.38%
CYP inhibitory promiscuity - 0.7039 70.39%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5883 58.83%
Carcinogenicity (trinary) Non-required 0.5480 54.80%
Eye corrosion + 0.8152 81.52%
Eye irritation + 0.9756 97.56%
Skin irritation + 0.7939 79.39%
Skin corrosion - 0.7700 77.00%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4873 48.73%
Micronuclear - 0.9700 97.00%
Hepatotoxicity + 0.5323 53.23%
skin sensitisation + 0.9405 94.05%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.8875 88.75%
Nephrotoxicity + 0.5197 51.97%
Acute Oral Toxicity (c) III 0.7580 75.80%
Estrogen receptor binding - 0.9813 98.13%
Androgen receptor binding - 0.9517 95.17%
Thyroid receptor binding - 0.8811 88.11%
Glucocorticoid receptor binding - 0.8499 84.99%
Aromatase binding - 0.9022 90.22%
PPAR gamma - 0.8729 87.29%
Honey bee toxicity - 0.9410 94.10%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.8100 81.00%
Fish aquatic toxicity + 0.8892 88.92%

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
CHEMBL4040 P28482 MAP kinase ERK2 98.01% 83.82%
CHEMBL3401 O75469 Pregnane X receptor 88.24% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.68% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.29% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.98% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.81% 94.45%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 83.27% 87.67%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.09% 89.34%

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.
Thymus martinezii

Cross-Links

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PubChem 85768581
LOTUS LTS0181788
wikiData Q105153622