6-Hydroxy-7,8-dimethoxycoumarin

Details

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Internal ID 69371a17-9286-49fe-8db9-589a08907d5f
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins
IUPAC Name 6-hydroxy-7,8-dimethoxychromen-2-one
SMILES (Canonical) COC1=C(C=C2C=CC(=O)OC2=C1OC)O
SMILES (Isomeric) COC1=C(C=C2C=CC(=O)OC2=C1OC)O
InChI InChI=1S/C11H10O5/c1-14-10-7(12)5-6-3-4-8(13)16-9(6)11(10)15-2/h3-5,12H,1-2H3
InChI Key ULJXDXSBXDSMLE-UHFFFAOYSA-N
Popularity 7 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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6-hydroxy-7,8-dimethoxy-chromen-2-one
CHEMBL469432
7,8-Dimethoxy-6-hydroxy cumarine

2D Structure

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2D Structure of 6-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 + 0.7008 70.08%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6686 66.86%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9282 92.82%
OATP1B3 inhibitior + 0.9746 97.46%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.7309 73.09%
P-glycoprotein inhibitior - 0.8869 88.69%
P-glycoprotein substrate - 0.9824 98.24%
CYP3A4 substrate - 0.7105 71.05%
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 - 0.8944 89.44%
CYP inhibitory promiscuity - 0.6635 66.35%
UGT catelyzed + 0.7362 73.62%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6010 60.10%
Eye corrosion - 0.9585 95.85%
Eye irritation + 0.8816 88.16%
Skin irritation - 0.6008 60.08%
Skin corrosion - 0.9837 98.37%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6194 61.94%
Micronuclear + 0.9059 90.59%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.9324 93.24%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.6710 67.10%
Acute Oral Toxicity (c) II 0.6201 62.01%
Estrogen receptor binding + 0.7473 74.73%
Androgen receptor binding + 0.5557 55.57%
Thyroid receptor binding - 0.5715 57.15%
Glucocorticoid receptor binding - 0.6003 60.03%
Aromatase binding + 0.6473 64.73%
PPAR gamma + 0.5675 56.75%
Honey bee toxicity - 0.9635 96.35%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6500 65.00%
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 97.19% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.92% 94.00%
CHEMBL2581 P07339 Cathepsin D 88.66% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.22% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.60% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.34% 94.45%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.15% 99.15%
CHEMBL3401 O75469 Pregnane X receptor 83.63% 94.73%
CHEMBL4040 P28482 MAP kinase ERK2 80.81% 83.82%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.10% 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 monosperma
Diospyros maritima
Fraxinus chinensis
Fraxinus chinensis subsp. chinensis
Fraxinus stylosa
Haloxylon salicornicum

Cross-Links

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PubChem 11345068
NPASS NPC20511
LOTUS LTS0260835
wikiData Q105275173