7-Hydroxy-3-methoxy-6-(3-methylbut-2-enyl)chromen-2-one

Details

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Internal ID 89198472-71e6-4818-8302-72a2bdee793e
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins > 7-hydroxycoumarins
IUPAC Name 7-hydroxy-3-methoxy-6-(3-methylbut-2-enyl)chromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H16O4/c1-9(2)4-5-10-6-11-7-14(18-3)15(17)19-13(11)8-12(10)16/h4,6-8,16H,5H2,1-3H3
InChI Key KLGRCWHERPTUFN-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O4
Molecular Weight 260.28 g/mol
Exact Mass 260.10485899 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.02
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Hydroxy-3-methoxy-6-(3-methylbut-2-enyl)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 + 0.9894 98.94%
Caco-2 + 0.8049 80.49%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.6405 64.05%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9446 94.46%
OATP1B3 inhibitior + 0.8887 88.87%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5758 57.58%
P-glycoprotein inhibitior - 0.7960 79.60%
P-glycoprotein substrate - 0.7589 75.89%
CYP3A4 substrate - 0.5423 54.23%
CYP2C9 substrate - 0.6172 61.72%
CYP2D6 substrate - 0.8048 80.48%
CYP3A4 inhibition - 0.8846 88.46%
CYP2C9 inhibition - 0.5326 53.26%
CYP2C19 inhibition + 0.8312 83.12%
CYP2D6 inhibition - 0.6697 66.97%
CYP1A2 inhibition + 0.6910 69.10%
CYP2C8 inhibition - 0.8409 84.09%
CYP inhibitory promiscuity + 0.6680 66.80%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6563 65.63%
Eye corrosion - 0.9857 98.57%
Eye irritation + 0.6573 65.73%
Skin irritation - 0.7438 74.38%
Skin corrosion - 0.9700 97.00%
Ames mutagenesis - 0.6854 68.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5973 59.73%
Micronuclear - 0.5100 51.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.8178 81.78%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.4948 49.48%
Acute Oral Toxicity (c) III 0.6444 64.44%
Estrogen receptor binding + 0.9419 94.19%
Androgen receptor binding - 0.5434 54.34%
Thyroid receptor binding + 0.5436 54.36%
Glucocorticoid receptor binding + 0.7825 78.25%
Aromatase binding + 0.8148 81.48%
PPAR gamma + 0.6970 69.70%
Honey bee toxicity - 0.8971 89.71%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9920 99.20%

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 99.07% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.39% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.30% 86.33%
CHEMBL2581 P07339 Cathepsin D 91.39% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.82% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.59% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 89.33% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.67% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.05% 95.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.07% 96.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.47% 92.62%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 14466225
LOTUS LTS0185131
wikiData Q105142612