5-Hydroxy-7,8-dimethoxycoumarin

Details

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Internal ID 1ca97398-b296-4d14-b84e-ea485a675a19
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins
IUPAC Name 5-hydroxy-7,8-dimethoxychromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H10O5/c1-14-8-5-7(12)6-3-4-9(13)16-10(6)11(8)15-2/h3-5,12H,1-2H3
InChI Key ZWEVIFVSDFJDJS-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C11H10O5
Molecular Weight 222.19 g/mol
Exact Mass 222.05282342 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.52
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Hydroxy-7,8-dimethoxycoumarin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9643 96.43%
Caco-2 + 0.6259 62.59%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.6686 66.86%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9500 95.00%
OATP1B3 inhibitior + 0.9746 97.46%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8123 81.23%
P-glycoprotein inhibitior - 0.8462 84.62%
P-glycoprotein substrate - 0.9199 91.99%
CYP3A4 substrate - 0.5920 59.20%
CYP2C9 substrate - 0.8431 84.31%
CYP2D6 substrate - 0.8139 81.39%
CYP3A4 inhibition - 0.7395 73.95%
CYP2C9 inhibition - 0.9291 92.91%
CYP2C19 inhibition - 0.7830 78.30%
CYP2D6 inhibition - 0.8714 87.14%
CYP1A2 inhibition + 0.8253 82.53%
CYP2C8 inhibition - 0.6431 64.31%
CYP inhibitory promiscuity - 0.6635 66.35%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6010 60.10%
Eye corrosion - 0.9585 95.85%
Eye irritation + 0.9206 92.06%
Skin irritation - 0.6008 60.08%
Skin corrosion - 0.9837 98.37%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7434 74.34%
Micronuclear + 0.9059 90.59%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.9324 93.24%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.7492 74.92%
Acute Oral Toxicity (c) II 0.6201 62.01%
Estrogen receptor binding + 0.8221 82.21%
Androgen receptor binding + 0.7206 72.06%
Thyroid receptor binding - 0.6245 62.45%
Glucocorticoid receptor binding + 0.7052 70.52%
Aromatase binding + 0.6764 67.64%
PPAR gamma - 0.5203 52.03%
Honey bee toxicity - 0.9188 91.88%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.5949 59.49%
Fish aquatic toxicity + 0.9128 91.28%

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 97.95% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 95.02% 83.82%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.28% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.21% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.03% 94.45%
CHEMBL2535 P11166 Glucose transporter 87.46% 98.75%
CHEMBL2581 P07339 Cathepsin D 86.75% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.59% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.81% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.24% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.84% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.59% 99.15%
CHEMBL3194 P02766 Transthyretin 83.03% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.21% 86.33%

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.
Artemisia laciniata

Cross-Links

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PubChem 5518297
LOTUS LTS0259045
wikiData Q105384877