5-Hydroxy-6-methoxychromen-2-one

Details

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Internal ID e4090535-f750-4593-b430-332bec01a681
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins
IUPAC Name 5-hydroxy-6-methoxychromen-2-one
SMILES (Canonical) COC1=C(C2=C(C=C1)OC(=O)C=C2)O
SMILES (Isomeric) COC1=C(C2=C(C=C1)OC(=O)C=C2)O
InChI InChI=1S/C10H8O4/c1-13-8-4-3-7-6(10(8)12)2-5-9(11)14-7/h2-5,12H,1H3
InChI Key CIWXNUFLRXYBQV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H8O4
Molecular Weight 192.17 g/mol
Exact Mass 192.04225873 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.51
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Hydroxy-6-methoxychromen-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9730 97.30%
Caco-2 + 0.5797 57.97%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.6806 68.06%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8595 85.95%
OATP1B3 inhibitior + 0.9915 99.15%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8256 82.56%
P-glycoprotein inhibitior - 0.9131 91.31%
P-glycoprotein substrate - 0.9150 91.50%
CYP3A4 substrate - 0.5783 57.83%
CYP2C9 substrate - 0.8431 84.31%
CYP2D6 substrate - 0.8139 81.39%
CYP3A4 inhibition - 0.7933 79.33%
CYP2C9 inhibition - 0.9071 90.71%
CYP2C19 inhibition - 0.7862 78.62%
CYP2D6 inhibition - 0.9230 92.30%
CYP1A2 inhibition + 0.9106 91.06%
CYP2C8 inhibition - 0.6968 69.68%
CYP inhibitory promiscuity - 0.6876 68.76%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5260 52.60%
Eye corrosion - 0.9431 94.31%
Eye irritation + 0.9822 98.22%
Skin irritation + 0.4950 49.50%
Skin corrosion - 0.9810 98.10%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7038 70.38%
Micronuclear + 0.9059 90.59%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.9369 93.69%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.7053 70.53%
Acute Oral Toxicity (c) III 0.8059 80.59%
Estrogen receptor binding + 0.8555 85.55%
Androgen receptor binding + 0.5679 56.79%
Thyroid receptor binding - 0.7240 72.40%
Glucocorticoid receptor binding + 0.6152 61.52%
Aromatase binding + 0.6638 66.38%
PPAR gamma - 0.6066 60.66%
Honey bee toxicity - 0.9306 93.06%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.6049 60.49%
Fish aquatic toxicity + 0.8914 89.14%

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 96.36% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.02% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.85% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.11% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.77% 99.23%
CHEMBL2581 P07339 Cathepsin D 88.07% 98.95%
CHEMBL1255126 O15151 Protein Mdm4 86.30% 90.20%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.99% 89.00%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 83.88% 94.03%
CHEMBL1951 P21397 Monoamine oxidase A 83.69% 91.49%

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.
Fraxinus floribunda
Prunus spinosa

Cross-Links

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PubChem 71440520
LOTUS LTS0194357
wikiData Q105126990