8-Hydroxy-6-methoxy-3-methylisocoumarin

Details

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Internal ID 23c351f6-3420-48f1-985e-d2911e87369c
Taxonomy Phenylpropanoids and polyketides > Isocoumarins and derivatives
IUPAC Name 8-hydroxy-6-methoxy-3-methylisochromen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H10O4/c1-6-3-7-4-8(14-2)5-9(12)10(7)11(13)15-6/h3-5,12H,1-2H3
InChI Key BZMCHKXIXROMSY-UHFFFAOYSA-N
Popularity 12 references 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) 55.80 Ų
XlogP 2.50
Atomic LogP (AlogP) 1.82
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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8-hydroxy-6-methoxy-3-methylisochromen-1-one
RefChem:914576
1702-86-9
SCHEMBL5079030
CHEBI:217431
6-Methoxy-3-methyl-8-hydroxy-1H-2-benzopyran-1-one

2D Structure

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2D Structure of 8-Hydroxy-6-methoxy-3-methylisocoumarin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9776 97.76%
Caco-2 + 0.7941 79.41%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6329 63.29%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9416 94.16%
OATP1B3 inhibitior + 0.9639 96.39%
MATE1 inhibitior - 0.6800 68.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8639 86.39%
P-glycoprotein inhibitior - 0.8841 88.41%
P-glycoprotein substrate - 0.9542 95.42%
CYP3A4 substrate - 0.5477 54.77%
CYP2C9 substrate - 0.5374 53.74%
CYP2D6 substrate - 0.8728 87.28%
CYP3A4 inhibition - 0.5292 52.92%
CYP2C9 inhibition - 0.7855 78.55%
CYP2C19 inhibition - 0.7891 78.91%
CYP2D6 inhibition - 0.8559 85.59%
CYP1A2 inhibition + 0.8351 83.51%
CYP2C8 inhibition - 0.8292 82.92%
CYP inhibitory promiscuity - 0.7180 71.80%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9213 92.13%
Carcinogenicity (trinary) Non-required 0.5597 55.97%
Eye corrosion - 0.9192 91.92%
Eye irritation + 0.9333 93.33%
Skin irritation - 0.6545 65.45%
Skin corrosion - 0.9895 98.95%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7521 75.21%
Micronuclear + 0.9100 91.00%
Hepatotoxicity - 0.5217 52.17%
skin sensitisation - 0.9602 96.02%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.5263 52.63%
Acute Oral Toxicity (c) III 0.5655 56.55%
Estrogen receptor binding - 0.5720 57.20%
Androgen receptor binding + 0.6661 66.61%
Thyroid receptor binding - 0.6301 63.01%
Glucocorticoid receptor binding - 0.5785 57.85%
Aromatase binding + 0.5940 59.40%
PPAR gamma + 0.5730 57.30%
Honey bee toxicity - 0.9269 92.69%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.8510 85.10%

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 96.51% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.42% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.21% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.25% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 88.67% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 88.56% 93.65%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.36% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.97% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.92% 99.23%
CHEMBL4208 P20618 Proteasome component C5 85.82% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.81% 85.14%
CHEMBL2581 P07339 Cathepsin D 83.37% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.44% 93.99%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 81.94% 94.42%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 80.36% 92.68%

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 gilvescens
Datura stramonium
Oenanthe fistulosa

Cross-Links

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PubChem 11127420
NPASS NPC127590
LOTUS LTS0028094
wikiData Q77565362