2,5,7,3',4'-Pentahydroxy-3,4-flavandione

Details

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Internal ID 16b73a3a-178c-4e8b-8d79-444850a99528
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > Flavanones
IUPAC Name 2-(3,4-dihydroxyphenyl)-2,5,7-trihydroxychromene-3,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H10O8/c16-7-4-10(19)12-11(5-7)23-15(22,14(21)13(12)20)6-1-2-8(17)9(18)3-6/h1-5,16-19,22H
InChI Key WDHJJAXPRDKDBA-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H10O8
Molecular Weight 318.23 g/mol
Exact Mass 318.03756727 g/mol
Topological Polar Surface Area (TPSA) 145.00 Ų
XlogP 1.10
Atomic LogP (AlogP) 0.50
H-Bond Acceptor 8
H-Bond Donor 5
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,5,7,3',4'-Pentahydroxy-3,4-flavandione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6672 66.72%
Caco-2 - 0.7794 77.94%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.6283 62.83%
OATP2B1 inhibitior - 0.6657 66.57%
OATP1B1 inhibitior + 0.9524 95.24%
OATP1B3 inhibitior + 0.9499 94.99%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9023 90.23%
P-glycoprotein inhibitior - 0.9365 93.65%
P-glycoprotein substrate - 0.9545 95.45%
CYP3A4 substrate - 0.5553 55.53%
CYP2C9 substrate - 0.8166 81.66%
CYP2D6 substrate - 0.8373 83.73%
CYP3A4 inhibition - 0.6750 67.50%
CYP2C9 inhibition - 0.7493 74.93%
CYP2C19 inhibition - 0.9203 92.03%
CYP2D6 inhibition - 0.9709 97.09%
CYP1A2 inhibition - 0.8585 85.85%
CYP2C8 inhibition - 0.6087 60.87%
CYP inhibitory promiscuity - 0.8947 89.47%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6983 69.83%
Eye corrosion - 0.9926 99.26%
Eye irritation + 0.9560 95.60%
Skin irritation - 0.5174 51.74%
Skin corrosion - 0.9300 93.00%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8806 88.06%
Micronuclear + 0.8900 89.00%
Hepatotoxicity - 0.5194 51.94%
skin sensitisation - 0.8665 86.65%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.7511 75.11%
Acute Oral Toxicity (c) II 0.5783 57.83%
Estrogen receptor binding + 0.6858 68.58%
Androgen receptor binding + 0.8421 84.21%
Thyroid receptor binding + 0.5698 56.98%
Glucocorticoid receptor binding + 0.7985 79.85%
Aromatase binding + 0.7812 78.12%
PPAR gamma + 0.6618 66.18%
Honey bee toxicity - 0.8252 82.52%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9633 96.33%

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 99.19% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.31% 95.56%
CHEMBL1929 P47989 Xanthine dehydrogenase 92.02% 96.12%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.68% 94.45%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.46% 99.15%
CHEMBL2581 P07339 Cathepsin D 90.95% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.78% 89.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 87.98% 93.40%
CHEMBL3194 P02766 Transthyretin 87.05% 90.71%
CHEMBL4208 P20618 Proteasome component C5 86.37% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.27% 99.23%
CHEMBL1951 P21397 Monoamine oxidase A 85.20% 91.49%

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.
Allium cepa

Cross-Links

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PubChem 14826843
LOTUS LTS0246545
wikiData Q105302369