7-Methoxy-5-(3-methylbut-2-enoxy)-8-(3-methylbut-2-enoyl)chromen-2-one

Details

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Internal ID 2b4bb321-e47e-4401-b4ac-76f35e9d4dd7
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 7-methoxy-5-(3-methylbut-2-enoxy)-8-(3-methylbut-2-enoyl)chromen-2-one
SMILES (Canonical) CC(=CCOC1=CC(=C(C2=C1C=CC(=O)O2)C(=O)C=C(C)C)OC)C
SMILES (Isomeric) CC(=CCOC1=CC(=C(C2=C1C=CC(=O)O2)C(=O)C=C(C)C)OC)C
InChI InChI=1S/C20H22O5/c1-12(2)8-9-24-16-11-17(23-5)19(15(21)10-13(3)4)20-14(16)6-7-18(22)25-20/h6-8,10-11H,9H2,1-5H3
InChI Key KMLONNDXWAQAPV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H22O5
Molecular Weight 342.40 g/mol
Exact Mass 342.14672380 g/mol
Topological Polar Surface Area (TPSA) 61.80 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.30
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Methoxy-5-(3-methylbut-2-enoxy)-8-(3-methylbut-2-enoyl)chromen-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 + 0.9919 99.19%
Caco-2 + 0.7627 76.27%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.7580 75.80%
OATP2B1 inhibitior - 0.8592 85.92%
OATP1B1 inhibitior + 0.9041 90.41%
OATP1B3 inhibitior + 0.9389 93.89%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8406 84.06%
P-glycoprotein inhibitior + 0.7734 77.34%
P-glycoprotein substrate - 0.6300 63.00%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.6133 61.33%
CYP2D6 substrate - 0.8906 89.06%
CYP3A4 inhibition - 0.7300 73.00%
CYP2C9 inhibition + 0.7302 73.02%
CYP2C19 inhibition + 0.9118 91.18%
CYP2D6 inhibition - 0.7447 74.47%
CYP1A2 inhibition + 0.9600 96.00%
CYP2C8 inhibition + 0.5614 56.14%
CYP inhibitory promiscuity + 0.8583 85.83%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9613 96.13%
Carcinogenicity (trinary) Non-required 0.7357 73.57%
Eye corrosion - 0.9812 98.12%
Eye irritation - 0.6327 63.27%
Skin irritation - 0.8174 81.74%
Skin corrosion - 0.9746 97.46%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7622 76.22%
Micronuclear - 0.5226 52.26%
Hepatotoxicity + 0.8000 80.00%
skin sensitisation - 0.7751 77.51%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.7188 71.88%
Acute Oral Toxicity (c) III 0.7054 70.54%
Estrogen receptor binding + 0.8694 86.94%
Androgen receptor binding + 0.8367 83.67%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.7382 73.82%
Aromatase binding + 0.8333 83.33%
PPAR gamma + 0.8012 80.12%
Honey bee toxicity - 0.8914 89.14%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9963 99.63%

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 97.67% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.38% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.69% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.44% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.05% 94.00%
CHEMBL2581 P07339 Cathepsin D 89.04% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 88.53% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.63% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.04% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.92% 86.33%
CHEMBL2535 P11166 Glucose transporter 85.96% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.86% 96.09%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 85.84% 97.21%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.04% 85.14%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.68% 96.95%

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.
Alstonia angustiloba
Alstonia scholaris
Angelica pubescens

Cross-Links

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PubChem 163089234
LOTUS LTS0123649
wikiData Q104397268