6,7,8-Trihydroxy-2H-1-benzopyran-2-one

Details

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Internal ID 0af118a8-b152-446a-81d3-2f91dbd012c1
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins > 7-hydroxycoumarins
IUPAC Name 6,7,8-trihydroxychromen-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H6O5/c10-5-3-4-1-2-6(11)14-9(4)8(13)7(5)12/h1-3,10,12-13H
InChI Key NSDVPAHANCHBFV-UHFFFAOYSA-N
Popularity 12 references in papers

Physical and Chemical Properties

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Molecular Formula C9H6O5
Molecular Weight 194.14 g/mol
Exact Mass 194.02152329 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.91
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

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6,7,8-Trihydroxy-2H-1-benzopyran-2-one
114371-80-1
SCHEMBL4658019
CHEMBL4171780
DTXSID70473747
CHEBI:178006
NSDVPAHANCHBFV-UHFFFAOYSA-N
AKOS000277571

2D Structure

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2D Structure of 6,7,8-Trihydroxy-2H-1-benzopyran-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 + 0.8131 81.31%
Caco-2 - 0.6258 62.58%
Blood Brain Barrier - 0.8250 82.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.5191 51.91%
OATP2B1 inhibitior - 0.7233 72.33%
OATP1B1 inhibitior + 0.8930 89.30%
OATP1B3 inhibitior + 0.9057 90.57%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9179 91.79%
P-glycoprotein inhibitior - 0.9604 96.04%
P-glycoprotein substrate - 0.9887 98.87%
CYP3A4 substrate - 0.7520 75.20%
CYP2C9 substrate - 0.8283 82.83%
CYP2D6 substrate - 0.8434 84.34%
CYP3A4 inhibition - 0.6514 65.14%
CYP2C9 inhibition - 0.9486 94.86%
CYP2C19 inhibition - 0.9671 96.71%
CYP2D6 inhibition - 0.9543 95.43%
CYP1A2 inhibition + 0.6409 64.09%
CYP2C8 inhibition - 0.8858 88.58%
CYP inhibitory promiscuity - 0.8110 81.10%
UGT catelyzed + 0.7362 73.62%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6928 69.28%
Eye corrosion - 0.9893 98.93%
Eye irritation + 0.9718 97.18%
Skin irritation + 0.6288 62.88%
Skin corrosion - 0.9538 95.38%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8612 86.12%
Micronuclear + 0.9400 94.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.6721 67.21%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.7687 76.87%
Acute Oral Toxicity (c) II 0.4771 47.71%
Estrogen receptor binding + 0.7465 74.65%
Androgen receptor binding + 0.7551 75.51%
Thyroid receptor binding - 0.5135 51.35%
Glucocorticoid receptor binding + 0.8475 84.75%
Aromatase binding - 0.4879 48.79%
PPAR gamma + 0.7904 79.04%
Honey bee toxicity - 0.9754 97.54%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9335 93.35%

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 97.97% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.42% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.51% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.01% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 85.60% 94.73%
CHEMBL2581 P07339 Cathepsin D 85.53% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.03% 99.23%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.85% 90.71%
CHEMBL3194 P02766 Transthyretin 81.73% 90.71%

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.
Didymocheton variabilis
Paramignya monophylla
Pelargonium sidoides

Cross-Links

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PubChem 11819936
LOTUS LTS0181089
wikiData Q105327535