7-Hydroxy-4,8-dimethoxy-2-oxochromene-5,6-dicarboxylic acid

Details

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Internal ID 2b43d8dc-73cd-4f46-8d8f-408d22bc3c61
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins > 7-hydroxycoumarins
IUPAC Name 7-hydroxy-4,8-dimethoxy-2-oxochromene-5,6-dicarboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H10O9/c1-20-4-3-5(14)22-10-6(4)7(12(16)17)8(13(18)19)9(15)11(10)21-2/h3,15H,1-2H3,(H,16,17)(H,18,19)
InChI Key HXFCTKKFLJMYHC-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H10O9
Molecular Weight 310.21 g/mol
Exact Mass 310.03248189 g/mol
Topological Polar Surface Area (TPSA) 140.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.91
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Hydroxy-4,8-dimethoxy-2-oxochromene-5,6-dicarboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8134 81.34%
Caco-2 - 0.5787 57.87%
Blood Brain Barrier - 0.9000 90.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.5551 55.51%
OATP2B1 inhibitior - 0.7145 71.45%
OATP1B1 inhibitior + 0.9119 91.19%
OATP1B3 inhibitior + 0.9006 90.06%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8804 88.04%
P-glycoprotein inhibitior - 0.8469 84.69%
P-glycoprotein substrate - 0.9115 91.15%
CYP3A4 substrate - 0.5847 58.47%
CYP2C9 substrate - 0.5681 56.81%
CYP2D6 substrate - 0.8904 89.04%
CYP3A4 inhibition - 0.7851 78.51%
CYP2C9 inhibition - 0.8081 80.81%
CYP2C19 inhibition - 0.8889 88.89%
CYP2D6 inhibition - 0.8468 84.68%
CYP1A2 inhibition + 0.5484 54.84%
CYP2C8 inhibition - 0.6603 66.03%
CYP inhibitory promiscuity - 0.6704 67.04%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.6653 66.53%
Eye corrosion - 0.9794 97.94%
Eye irritation + 0.5709 57.09%
Skin irritation - 0.6936 69.36%
Skin corrosion - 0.9430 94.30%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7256 72.56%
Micronuclear + 0.9200 92.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.9283 92.83%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.6784 67.84%
Acute Oral Toxicity (c) III 0.4991 49.91%
Estrogen receptor binding + 0.6566 65.66%
Androgen receptor binding + 0.5644 56.44%
Thyroid receptor binding - 0.7955 79.55%
Glucocorticoid receptor binding + 0.6294 62.94%
Aromatase binding - 0.6316 63.16%
PPAR gamma + 0.8022 80.22%
Honey bee toxicity - 0.9423 94.23%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.9268 92.68%

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 97.01% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.63% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.76% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.46% 94.00%
CHEMBL1255126 O15151 Protein Mdm4 90.51% 90.20%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.11% 99.23%
CHEMBL3194 P02766 Transthyretin 88.57% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.24% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.70% 85.14%
CHEMBL213 P08588 Beta-1 adrenergic receptor 85.81% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.25% 99.17%
CHEMBL2581 P07339 Cathepsin D 84.85% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.11% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.76% 89.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 82.87% 94.42%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.37% 89.34%
CHEMBL2535 P11166 Glucose transporter 81.72% 98.75%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.13% 95.50%

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.
Sanguisorba minor

Cross-Links

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PubChem 91554824
LOTUS LTS0117637
wikiData Q105034960