7-Hydroxy-3,4-dimethoxy-5-methylchromen-2-one

Details

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Internal ID 7631639d-d14a-40da-afe5-d11f588b575d
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins > 7-hydroxycoumarins
IUPAC Name 7-hydroxy-3,4-dimethoxy-5-methylchromen-2-one
SMILES (Canonical) CC1=CC(=CC2=C1C(=C(C(=O)O2)OC)OC)O
SMILES (Isomeric) CC1=CC(=CC2=C1C(=C(C(=O)O2)OC)OC)O
InChI InChI=1S/C12H12O5/c1-6-4-7(13)5-8-9(6)10(15-2)11(16-3)12(14)17-8/h4-5,13H,1-3H3
InChI Key AXLQMGBJLXYPHW-UHFFFAOYSA-N
Popularity 1 reference 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 1.80
Atomic LogP (AlogP) 1.82
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Hydroxy-3,4-dimethoxy-5-methylchromen-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 + 0.9602 96.02%
Caco-2 + 0.5427 54.27%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6514 65.14%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9339 93.39%
OATP1B3 inhibitior + 0.9611 96.11%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.7982 79.82%
P-glycoprotein inhibitior - 0.8845 88.45%
P-glycoprotein substrate - 0.9597 95.97%
CYP3A4 substrate - 0.5484 54.84%
CYP2C9 substrate - 0.6417 64.17%
CYP2D6 substrate - 0.8446 84.46%
CYP3A4 inhibition - 0.8520 85.20%
CYP2C9 inhibition - 0.9867 98.67%
CYP2C19 inhibition - 0.9199 91.99%
CYP2D6 inhibition - 0.9293 92.93%
CYP1A2 inhibition + 0.8260 82.60%
CYP2C8 inhibition - 0.7372 73.72%
CYP inhibitory promiscuity - 0.7249 72.49%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5526 55.26%
Eye corrosion - 0.9701 97.01%
Eye irritation + 0.9434 94.34%
Skin irritation - 0.6961 69.61%
Skin corrosion - 0.9873 98.73%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5862 58.62%
Micronuclear + 0.8459 84.59%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.9463 94.63%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6117 61.17%
Acute Oral Toxicity (c) II 0.6827 68.27%
Estrogen receptor binding + 0.7199 71.99%
Androgen receptor binding + 0.5919 59.19%
Thyroid receptor binding - 0.6683 66.83%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding + 0.6460 64.60%
PPAR gamma - 0.5256 52.56%
Honey bee toxicity - 0.7411 74.11%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9186 91.86%

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 96.47% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.89% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 91.33% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.18% 95.56%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 89.61% 93.65%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.34% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.60% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.01% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.11% 99.23%
CHEMBL2581 P07339 Cathepsin D 80.67% 98.95%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 80.40% 100.00%

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.
Dolichlasium lagascae
Sideritis cretica subsp. spicata

Cross-Links

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PubChem 162974845
LOTUS LTS0103112
wikiData Q104400450