7-(7-Hydroxy-3,7-dimethylocta-2,5-dienoxy)-6-methoxychromen-2-one

Details

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Internal ID a658b5a4-27ff-4bef-ad69-5190ca3c5e8b
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 7-(7-hydroxy-3,7-dimethylocta-2,5-dienoxy)-6-methoxychromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H24O5/c1-14(6-5-10-20(2,3)22)9-11-24-18-13-16-15(12-17(18)23-4)7-8-19(21)25-16/h5,7-10,12-13,22H,6,11H2,1-4H3
InChI Key RZHGIBONLJZHIW-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H24O5
Molecular Weight 344.40 g/mol
Exact Mass 344.16237386 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.84
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-(7-Hydroxy-3,7-dimethylocta-2,5-dienoxy)-6-methoxychromen-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 + 0.9695 96.95%
Caco-2 + 0.6967 69.67%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7623 76.23%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8685 86.85%
OATP1B3 inhibitior + 0.9056 90.56%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9488 94.88%
P-glycoprotein inhibitior + 0.6396 63.96%
P-glycoprotein substrate - 0.6993 69.93%
CYP3A4 substrate + 0.5494 54.94%
CYP2C9 substrate - 0.6340 63.40%
CYP2D6 substrate - 0.8186 81.86%
CYP3A4 inhibition - 0.5740 57.40%
CYP2C9 inhibition + 0.6497 64.97%
CYP2C19 inhibition + 0.8367 83.67%
CYP2D6 inhibition - 0.7557 75.57%
CYP1A2 inhibition + 0.8793 87.93%
CYP2C8 inhibition + 0.5529 55.29%
CYP inhibitory promiscuity + 0.6021 60.21%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6741 67.41%
Eye corrosion - 0.9910 99.10%
Eye irritation - 0.8730 87.30%
Skin irritation - 0.7720 77.20%
Skin corrosion - 0.9618 96.18%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8705 87.05%
Micronuclear - 0.6700 67.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.7942 79.42%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.7106 71.06%
Acute Oral Toxicity (c) III 0.5593 55.93%
Estrogen receptor binding + 0.9180 91.80%
Androgen receptor binding + 0.5587 55.87%
Thyroid receptor binding + 0.6865 68.65%
Glucocorticoid receptor binding + 0.8285 82.85%
Aromatase binding + 0.7277 72.77%
PPAR gamma + 0.8069 80.69%
Honey bee toxicity - 0.8915 89.15%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 1.0000 100.00%

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 94.24% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 93.55% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.45% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.13% 94.00%
CHEMBL2581 P07339 Cathepsin D 90.26% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.85% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.91% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 85.73% 94.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.48% 96.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.43% 96.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.94% 89.00%
CHEMBL4208 P20618 Proteasome component C5 84.72% 90.00%
CHEMBL2535 P11166 Glucose transporter 84.39% 98.75%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 82.01% 92.38%

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.
Zanthoxylum schinifolium

Cross-Links

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PubChem 162883818
LOTUS LTS0037109
wikiData Q105248386