5,8-Dimethoxycoumarin

Details

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Internal ID a7fdf04d-a91d-449a-b6c0-c2d296bcc7aa
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 5,8-dimethoxychromen-2-one
SMILES (Canonical) COC1=C2C=CC(=O)OC2=C(C=C1)OC
SMILES (Isomeric) COC1=C2C=CC(=O)OC2=C(C=C1)OC
InChI InChI=1S/C11H10O4/c1-13-8-4-5-9(14-2)11-7(8)3-6-10(12)15-11/h3-6H,1-2H3
InChI Key YITSCFOPPAUZLM-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C11H10O4
Molecular Weight 206.19 g/mol
Exact Mass 206.05790880 g/mol
Topological Polar Surface Area (TPSA) 44.80 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.81
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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2H-1-Benzopyran-2-one, 5,8-dimethoxy-
5,8-Dimethoxycumarin
57585-52-1
DTXSID90346126
YITSCFOPPAUZLM-UHFFFAOYSA-N
5,8-Dimethoxy-2H-chromen-2-one #

2D Structure

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2D Structure of 5,8-Dimethoxycoumarin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9815 98.15%
Caco-2 + 0.8246 82.46%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.5320 53.20%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9628 96.28%
OATP1B3 inhibitior + 0.9218 92.18%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.7969 79.69%
P-glycoprotein inhibitior - 0.8833 88.33%
P-glycoprotein substrate - 0.9250 92.50%
CYP3A4 substrate - 0.6499 64.99%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8151 81.51%
CYP3A4 inhibition + 0.5292 52.92%
CYP2C9 inhibition - 0.8525 85.25%
CYP2C19 inhibition + 0.5358 53.58%
CYP2D6 inhibition - 0.8152 81.52%
CYP1A2 inhibition + 0.9531 95.31%
CYP2C8 inhibition - 0.8482 84.82%
CYP inhibitory promiscuity + 0.5466 54.66%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5381 53.81%
Eye corrosion - 0.8268 82.68%
Eye irritation + 0.9591 95.91%
Skin irritation - 0.6573 65.73%
Skin corrosion - 0.9879 98.79%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3956 39.56%
Micronuclear + 0.8400 84.00%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation - 0.9136 91.36%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.5084 50.84%
Acute Oral Toxicity (c) II 0.5189 51.89%
Estrogen receptor binding - 0.5579 55.79%
Androgen receptor binding + 0.6920 69.20%
Thyroid receptor binding - 0.7296 72.96%
Glucocorticoid receptor binding - 0.5537 55.37%
Aromatase binding + 0.5413 54.13%
PPAR gamma - 0.5548 55.48%
Honey bee toxicity - 0.8796 87.96%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.8596 85.96%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.59% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.82% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.09% 94.45%
CHEMBL2581 P07339 Cathepsin D 85.83% 98.95%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 83.35% 94.03%
CHEMBL1255126 O15151 Protein Mdm4 82.41% 90.20%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.37% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.09% 96.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.78% 99.23%

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.
Angelica decursiva
Kitagawia praeruptora

Cross-Links

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PubChem 609839
NPASS NPC230091