3-Acetoxymethyl-6,8-dimethoxycoumarin

Details

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Internal ID a94e5490-6093-458d-b600-59068d12614c
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name (6,8-dimethoxy-2-oxochromen-3-yl)methyl acetate
SMILES (Canonical) CC(=O)OCC1=CC2=CC(=CC(=C2OC1=O)OC)OC
SMILES (Isomeric) CC(=O)OCC1=CC2=CC(=CC(=C2OC1=O)OC)OC
InChI InChI=1S/C14H14O6/c1-8(15)19-7-10-4-9-5-11(17-2)6-12(18-3)13(9)20-14(10)16/h4-6H,7H2,1-3H3
InChI Key YGGLDHBOJBUAPL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C14H14O6
Molecular Weight 278.26 g/mol
Exact Mass 278.07903816 g/mol
Topological Polar Surface Area (TPSA) 71.10 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.87
H-Bond Acceptor 6
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Acetoxymethyl-6,8-dimethoxycoumarin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9728 97.28%
Caco-2 + 0.7453 74.53%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6190 61.90%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9229 92.29%
OATP1B3 inhibitior + 0.9235 92.35%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6204 62.04%
P-glycoprotein inhibitior - 0.7607 76.07%
P-glycoprotein substrate - 0.8973 89.73%
CYP3A4 substrate - 0.5276 52.76%
CYP2C9 substrate - 0.8235 82.35%
CYP2D6 substrate - 0.8606 86.06%
CYP3A4 inhibition - 0.8412 84.12%
CYP2C9 inhibition - 0.7206 72.06%
CYP2C19 inhibition - 0.6869 68.69%
CYP2D6 inhibition - 0.9273 92.73%
CYP1A2 inhibition + 0.8307 83.07%
CYP2C8 inhibition - 0.6614 66.14%
CYP inhibitory promiscuity + 0.5268 52.68%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7033 70.33%
Eye corrosion - 0.9654 96.54%
Eye irritation + 0.5711 57.11%
Skin irritation - 0.8344 83.44%
Skin corrosion - 0.9793 97.93%
Ames mutagenesis - 0.6354 63.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5438 54.38%
Micronuclear + 0.5192 51.92%
Hepatotoxicity - 0.5600 56.00%
skin sensitisation - 0.8981 89.81%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.6186 61.86%
Acute Oral Toxicity (c) III 0.5623 56.23%
Estrogen receptor binding + 0.7971 79.71%
Androgen receptor binding + 0.6950 69.50%
Thyroid receptor binding - 0.5079 50.79%
Glucocorticoid receptor binding + 0.5599 55.99%
Aromatase binding + 0.6175 61.75%
PPAR gamma - 0.5654 56.54%
Honey bee toxicity - 0.9151 91.51%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9740 97.40%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.76% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.58% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.19% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.99% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.14% 86.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.21% 92.62%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.00% 96.00%
CHEMBL2581 P07339 Cathepsin D 86.94% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.31% 95.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.26% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 83.56% 94.73%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.61% 95.50%
CHEMBL4208 P20618 Proteasome component C5 81.61% 90.00%
CHEMBL2535 P11166 Glucose transporter 81.11% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.58% 96.09%

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 139591605
LOTUS LTS0010210
wikiData Q104201670