(2E)-1-(2,5-dihydroxyphenyl)-3,7-dimethylocta-2,6-dien-1-one

Details

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Internal ID f386b256-c4c1-445f-9e89-f4353c0a4715
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Quinone and hydroquinone lipids > Prenylated hydroquinones
IUPAC Name (2E)-1-(2,5-dihydroxyphenyl)-3,7-dimethylocta-2,6-dien-1-one
SMILES (Canonical) CC(=CCCC(=CC(=O)C1=C(C=CC(=C1)O)O)C)C
SMILES (Isomeric) CC(=CCC/C(=C/C(=O)C1=C(C=CC(=C1)O)O)/C)C
InChI InChI=1S/C16H20O3/c1-11(2)5-4-6-12(3)9-16(19)14-10-13(17)7-8-15(14)18/h5,7-10,17-18H,4,6H2,1-3H3/b12-9+
InChI Key GUDWMKNWJMHSCP-FMIVXFBMSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H20O3
Molecular Weight 260.33 g/mol
Exact Mass 260.14124450 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 4.80
Atomic LogP (AlogP) 3.97
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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SCHEMBL13952721

2D Structure

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2D Structure of (2E)-1-(2,5-dihydroxyphenyl)-3,7-dimethylocta-2,6-dien-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8107 81.07%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.8226 82.26%
OATP2B1 inhibitior - 0.8528 85.28%
OATP1B1 inhibitior + 0.9007 90.07%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.5205 52.05%
P-glycoprotein inhibitior - 0.9399 93.99%
P-glycoprotein substrate - 0.9000 90.00%
CYP3A4 substrate - 0.6031 60.31%
CYP2C9 substrate - 0.7770 77.70%
CYP2D6 substrate - 0.8482 84.82%
CYP3A4 inhibition - 0.6328 63.28%
CYP2C9 inhibition + 0.7027 70.27%
CYP2C19 inhibition + 0.7209 72.09%
CYP2D6 inhibition - 0.7196 71.96%
CYP1A2 inhibition + 0.9010 90.10%
CYP2C8 inhibition - 0.7982 79.82%
CYP inhibitory promiscuity + 0.6859 68.59%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6701 67.01%
Carcinogenicity (trinary) Non-required 0.6660 66.60%
Eye corrosion - 0.9567 95.67%
Eye irritation + 0.6924 69.24%
Skin irritation - 0.5281 52.81%
Skin corrosion - 0.8734 87.34%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5740 57.40%
Micronuclear - 0.8500 85.00%
Hepatotoxicity + 0.5565 55.65%
skin sensitisation + 0.7986 79.86%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.5856 58.56%
Acute Oral Toxicity (c) III 0.7804 78.04%
Estrogen receptor binding + 0.7503 75.03%
Androgen receptor binding + 0.7115 71.15%
Thyroid receptor binding + 0.5501 55.01%
Glucocorticoid receptor binding + 0.7063 70.63%
Aromatase binding + 0.6243 62.43%
PPAR gamma + 0.9030 90.30%
Honey bee toxicity - 0.9251 92.51%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.9937 99.37%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.04% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.03% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.14% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.93% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 90.93% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.90% 99.17%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 89.22% 93.10%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 87.28% 92.08%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.59% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.31% 86.33%
CHEMBL4208 P20618 Proteasome component C5 81.45% 90.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.24% 90.71%

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.
Piper crassinervium

Cross-Links

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PubChem 10377908
LOTUS LTS0275441
wikiData Q105020044