(4E)-8-methylnona-4,7-dien-3-one

Details

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Internal ID 8ea28d08-f2b5-4bab-a015-f548b6617e8d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Alpha,beta-unsaturated ketones > Enones
IUPAC Name (4E)-8-methylnona-4,7-dien-3-one
SMILES (Canonical) CCC(=O)C=CCC=C(C)C
SMILES (Isomeric) CCC(=O)/C=C/CC=C(C)C
InChI InChI=1S/C10H16O/c1-4-10(11)8-6-5-7-9(2)3/h6-8H,4-5H2,1-3H3/b8-6+
InChI Key QFGBSMZKZAHNKE-SOFGYWHQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O
Molecular Weight 152.23 g/mol
Exact Mass 152.120115130 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.88
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 (4E)-8-methylnona-4,7-dien-3-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 + 0.9065 90.65%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.4837 48.37%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9334 93.34%
OATP1B3 inhibitior + 0.9513 95.13%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7403 74.03%
P-glycoprotein inhibitior - 0.9901 99.01%
P-glycoprotein substrate - 0.9612 96.12%
CYP3A4 substrate - 0.6775 67.75%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8620 86.20%
CYP3A4 inhibition - 0.9620 96.20%
CYP2C9 inhibition - 0.8680 86.80%
CYP2C19 inhibition - 0.8354 83.54%
CYP2D6 inhibition - 0.9276 92.76%
CYP1A2 inhibition - 0.7044 70.44%
CYP2C8 inhibition - 0.9577 95.77%
CYP inhibitory promiscuity - 0.6055 60.55%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5800 58.00%
Carcinogenicity (trinary) Non-required 0.6150 61.50%
Eye corrosion + 0.7826 78.26%
Eye irritation + 0.9905 99.05%
Skin irritation + 0.8054 80.54%
Skin corrosion - 0.7065 70.65%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5907 59.07%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.7000 70.00%
skin sensitisation + 0.9376 93.76%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity - 0.6078 60.78%
Acute Oral Toxicity (c) III 0.7763 77.63%
Estrogen receptor binding - 0.9521 95.21%
Androgen receptor binding - 0.8885 88.85%
Thyroid receptor binding - 0.8446 84.46%
Glucocorticoid receptor binding - 0.7565 75.65%
Aromatase binding - 0.7706 77.06%
PPAR gamma - 0.7182 71.82%
Honey bee toxicity - 0.9525 95.25%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.8073 80.73%

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
CHEMBL221 P23219 Cyclooxygenase-1 91.37% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.68% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.69% 89.34%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.47% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.70% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 81.26% 94.73%
CHEMBL2581 P07339 Cathepsin D 81.15% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.62% 91.11%

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.
Curculigo orchioides

Cross-Links

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PubChem 5319674
NPASS NPC157611