5-(3',3'-Dimethylallyl)-7,8-dihydroxy-6-methoxycoumarin

Details

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Internal ID 521a42c8-ab3a-4960-805c-5f0a8a62e9e3
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins > 7,8-dihydroxycoumarins
IUPAC Name 7,8-dihydroxy-6-methoxy-5-(3-methylbut-2-enyl)chromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H16O5/c1-8(2)4-5-9-10-6-7-11(16)20-15(10)13(18)12(17)14(9)19-3/h4,6-7,17-18H,5H2,1-3H3
InChI Key VCQOFWFYLXOGFZ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O5
Molecular Weight 276.28 g/mol
Exact Mass 276.09977361 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.72
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-(3',3'-Dimethylallyl)-7,8-dihydroxy-6-methoxycoumarin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9243 92.43%
Caco-2 + 0.7088 70.88%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.6414 64.14%
OATP2B1 inhibitior - 0.7232 72.32%
OATP1B1 inhibitior + 0.8548 85.48%
OATP1B3 inhibitior + 0.9215 92.15%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6248 62.48%
P-glycoprotein inhibitior - 0.8390 83.90%
P-glycoprotein substrate - 0.8349 83.49%
CYP3A4 substrate - 0.5510 55.10%
CYP2C9 substrate - 0.6141 61.41%
CYP2D6 substrate - 0.8133 81.33%
CYP3A4 inhibition - 0.9301 93.01%
CYP2C9 inhibition + 0.6359 63.59%
CYP2C19 inhibition + 0.7616 76.16%
CYP2D6 inhibition + 0.5000 50.00%
CYP1A2 inhibition + 0.7283 72.83%
CYP2C8 inhibition - 0.7384 73.84%
CYP inhibitory promiscuity + 0.6880 68.80%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6299 62.99%
Eye corrosion - 0.9894 98.94%
Eye irritation - 0.5206 52.06%
Skin irritation - 0.7452 74.52%
Skin corrosion - 0.9557 95.57%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5168 51.68%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation - 0.8200 82.00%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.8944 89.44%
Acute Oral Toxicity (c) III 0.6442 64.42%
Estrogen receptor binding + 0.7624 76.24%
Androgen receptor binding + 0.5201 52.01%
Thyroid receptor binding - 0.5547 55.47%
Glucocorticoid receptor binding + 0.8362 83.62%
Aromatase binding + 0.6447 64.47%
PPAR gamma + 0.7499 74.99%
Honey bee toxicity - 0.8809 88.09%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.9934 99.34%

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 99.12% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.05% 94.45%
CHEMBL2581 P07339 Cathepsin D 94.07% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.59% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 89.00% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.86% 94.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.25% 89.34%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.93% 96.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.65% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.30% 99.17%
CHEMBL3922 P50579 Methionine aminopeptidase 2 80.11% 97.28%

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.
Haplophyllum obtusifolium

Cross-Links

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PubChem 23263155
LOTUS LTS0233967
wikiData Q105283901