6,8-Dihydroxy-3-(hydroxymethyl)-1H-2-benzopyran-1-one

Details

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Internal ID 83e76d55-85a8-4636-a7f3-a477b807148b
Taxonomy Phenylpropanoids and polyketides > Isocoumarins and derivatives
IUPAC Name 6,8-dihydroxy-3-(hydroxymethyl)isochromen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H8O5/c11-4-7-2-5-1-6(12)3-8(13)9(5)10(14)15-7/h1-3,11-13H,4H2
InChI Key BKFBBKNNGTZBPF-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C10H8O5
Molecular Weight 208.17 g/mol
Exact Mass 208.03717335 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 0.90
Atomic LogP (AlogP) 0.70
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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62209-16-9
6,8-dihydroxy-3-(hydroxymethyl)isochromen-1-one
CHEMBL539432
6,8-Dihydroxy-3-(hydroxymethyl)-1H-2-benzopyran-1-one
SCHEMBL17866981
DTXSID80433771
CHEBI:198792
6,8-dihydroxy-3-hydroxymethyl isocou-marin

2D Structure

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2D Structure of 6,8-Dihydroxy-3-(hydroxymethyl)-1H-2-benzopyran-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8610 86.10%
Caco-2 + 0.5916 59.16%
Blood Brain Barrier - 0.8500 85.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.5435 54.35%
OATP2B1 inhibitior - 0.7096 70.96%
OATP1B1 inhibitior + 0.9108 91.08%
OATP1B3 inhibitior + 0.8433 84.33%
MATE1 inhibitior - 0.5200 52.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9262 92.62%
P-glycoprotein inhibitior - 0.9611 96.11%
P-glycoprotein substrate - 0.9439 94.39%
CYP3A4 substrate - 0.6213 62.13%
CYP2C9 substrate - 0.5401 54.01%
CYP2D6 substrate - 0.8721 87.21%
CYP3A4 inhibition - 0.7485 74.85%
CYP2C9 inhibition - 0.8912 89.12%
CYP2C19 inhibition - 0.9049 90.49%
CYP2D6 inhibition - 0.9352 93.52%
CYP1A2 inhibition - 0.8167 81.67%
CYP2C8 inhibition - 0.8333 83.33%
CYP inhibitory promiscuity - 0.6989 69.89%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6461 64.61%
Eye corrosion - 0.9833 98.33%
Eye irritation + 0.9573 95.73%
Skin irritation - 0.7084 70.84%
Skin corrosion - 0.9702 97.02%
Ames mutagenesis + 0.6063 60.63%
Human Ether-a-go-go-Related Gene inhibition - 0.9166 91.66%
Micronuclear + 0.5433 54.33%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.8552 85.52%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.4586 45.86%
Acute Oral Toxicity (c) II 0.4527 45.27%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding + 0.7260 72.60%
Thyroid receptor binding - 0.6681 66.81%
Glucocorticoid receptor binding + 0.7473 74.73%
Aromatase binding + 0.5397 53.97%
PPAR gamma + 0.7931 79.31%
Honey bee toxicity - 0.9266 92.66%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity - 0.4592 45.92%

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 97.85% 91.11%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.52% 93.99%
CHEMBL2581 P07339 Cathepsin D 88.10% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.82% 94.00%
CHEMBL1929 P47989 Xanthine dehydrogenase 87.67% 96.12%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.09% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.62% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 83.89% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.75% 99.17%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 82.96% 89.67%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.30% 89.00%
CHEMBL3194 P02766 Transthyretin 82.30% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.19% 86.33%

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.
Artemisia gilvescens
Datura stramonium
Oenanthe fistulosa

Cross-Links

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PubChem 9990614
NPASS NPC247409
LOTUS LTS0138100
wikiData Q75063164