3,8-Dihydroxy-4-methoxy-2-oxochromene-5-carboxylic acid

Details

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Internal ID 96b594aa-41e1-4ef5-ac36-43de31225ab6
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins
IUPAC Name 3,8-dihydroxy-4-methoxy-2-oxochromene-5-carboxylic acid
SMILES (Canonical) COC1=C(C(=O)OC2=C(C=CC(=C21)C(=O)O)O)O
SMILES (Isomeric) COC1=C(C(=O)OC2=C(C=CC(=C21)C(=O)O)O)O
InChI InChI=1S/C11H8O7/c1-17-9-6-4(10(14)15)2-3-5(12)8(6)18-11(16)7(9)13/h2-3,12-13H,1H3,(H,14,15)
InChI Key ZWHGKGZEJKYFFJ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C11H8O7
Molecular Weight 252.18 g/mol
Exact Mass 252.02700259 g/mol
Topological Polar Surface Area (TPSA) 113.00 Ų
XlogP 0.60
Atomic LogP (AlogP) 0.91
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,8-Dihydroxy-4-methoxy-2-oxochromene-5-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9226 92.26%
Caco-2 - 0.8460 84.60%
Blood Brain Barrier - 0.9000 90.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7310 73.10%
OATP2B1 inhibitior - 0.7204 72.04%
OATP1B1 inhibitior + 0.9470 94.70%
OATP1B3 inhibitior + 0.9822 98.22%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9223 92.23%
P-glycoprotein inhibitior - 0.8922 89.22%
P-glycoprotein substrate - 0.9456 94.56%
CYP3A4 substrate - 0.6429 64.29%
CYP2C9 substrate - 0.8036 80.36%
CYP2D6 substrate - 0.8742 87.42%
CYP3A4 inhibition - 0.9331 93.31%
CYP2C9 inhibition - 0.7108 71.08%
CYP2C19 inhibition - 0.8539 85.39%
CYP2D6 inhibition - 0.9261 92.61%
CYP1A2 inhibition + 0.8030 80.30%
CYP2C8 inhibition - 0.7376 73.76%
CYP inhibitory promiscuity - 0.7801 78.01%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5813 58.13%
Eye corrosion - 0.9718 97.18%
Eye irritation + 0.9630 96.30%
Skin irritation - 0.6211 62.11%
Skin corrosion - 0.9538 95.38%
Ames mutagenesis - 0.5064 50.64%
Human Ether-a-go-go-Related Gene inhibition - 0.8398 83.98%
Micronuclear + 0.9300 93.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.9464 94.64%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.6800 68.00%
Acute Oral Toxicity (c) III 0.7502 75.02%
Estrogen receptor binding + 0.7233 72.33%
Androgen receptor binding - 0.5443 54.43%
Thyroid receptor binding - 0.7550 75.50%
Glucocorticoid receptor binding + 0.7239 72.39%
Aromatase binding - 0.6979 69.79%
PPAR gamma + 0.6095 60.95%
Honey bee toxicity - 0.9552 95.52%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.8600 86.00%
Fish aquatic toxicity + 0.9270 92.70%

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 97.43% 91.11%
CHEMBL3194 P02766 Transthyretin 90.82% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.72% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.49% 94.00%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 89.92% 98.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.89% 99.23%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 89.78% 94.42%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 88.41% 81.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.09% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.29% 86.33%
CHEMBL2581 P07339 Cathepsin D 86.38% 98.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.07% 99.15%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.90% 89.34%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 83.67% 87.67%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.21% 99.17%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.87% 95.50%
CHEMBL1811 P34995 Prostanoid EP1 receptor 80.82% 95.71%

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.
Coptis chinensis
Euphorbia ebracteolata
Leibnitzia anandria

Cross-Links

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PubChem 3083044
NPASS NPC76468