7-(2-Hydroxyethoxy)-6-methoxychromen-2-one

Details

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Internal ID b55724cf-c517-4154-bd11-34278c5b4070
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 7-(2-hydroxyethoxy)-6-methoxychromen-2-one
SMILES (Canonical) COC1=C(C=C2C(=C1)C=CC(=O)O2)OCCO
SMILES (Isomeric) COC1=C(C=C2C(=C1)C=CC(=O)O2)OCCO
InChI InChI=1S/C12H12O5/c1-15-10-6-8-2-3-12(14)17-9(8)7-11(10)16-5-4-13/h2-3,6-7,13H,4-5H2,1H3
InChI Key FKPQJOGPSWNIAR-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H12O5
Molecular Weight 236.22 g/mol
Exact Mass 236.06847348 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.17
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-(2-Hydroxyethoxy)-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 + 0.9490 94.90%
Caco-2 + 0.7627 76.27%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.7277 72.77%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9014 90.14%
OATP1B3 inhibitior + 0.9648 96.48%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8155 81.55%
P-glycoprotein inhibitior - 0.9384 93.84%
P-glycoprotein substrate - 0.7434 74.34%
CYP3A4 substrate - 0.5886 58.86%
CYP2C9 substrate - 0.8464 84.64%
CYP2D6 substrate - 0.8131 81.31%
CYP3A4 inhibition - 0.8504 85.04%
CYP2C9 inhibition - 0.8459 84.59%
CYP2C19 inhibition - 0.7121 71.21%
CYP2D6 inhibition - 0.8835 88.35%
CYP1A2 inhibition - 0.5326 53.26%
CYP2C8 inhibition + 0.4766 47.66%
CYP inhibitory promiscuity - 0.7375 73.75%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6360 63.60%
Eye corrosion - 0.9784 97.84%
Eye irritation + 0.7472 74.72%
Skin irritation - 0.7812 78.12%
Skin corrosion - 0.9718 97.18%
Ames mutagenesis - 0.6737 67.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5318 53.18%
Micronuclear - 0.5467 54.67%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.8711 87.11%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.6023 60.23%
Acute Oral Toxicity (c) III 0.7301 73.01%
Estrogen receptor binding + 0.5846 58.46%
Androgen receptor binding + 0.6882 68.82%
Thyroid receptor binding - 0.7189 71.89%
Glucocorticoid receptor binding - 0.5095 50.95%
Aromatase binding + 0.5645 56.45%
PPAR gamma + 0.6440 64.40%
Honey bee toxicity - 0.9458 94.58%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.8100 81.00%
Fish aquatic toxicity - 0.6211 62.11%

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
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.06% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.59% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.37% 91.11%
CHEMBL2581 P07339 Cathepsin D 90.98% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.96% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.68% 96.09%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 86.65% 94.03%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 84.62% 86.92%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.37% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 82.92% 94.73%
CHEMBL1937 Q92769 Histone deacetylase 2 82.43% 94.75%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.15% 96.95%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.58% 90.71%
CHEMBL5555 O00767 Acyl-CoA desaturase 81.52% 97.50%

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.
Alstonia venenata
Pterocaulon polystachyum

Cross-Links

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PubChem 85800492
LOTUS LTS0128750
wikiData Q105285661