2,3,3,5,6-Pentahydroxy-2-phenylchromen-4-one

Details

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Internal ID 5ee41719-8798-41f6-a4c2-ad9156eb9c0e
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavans > Flavanones
IUPAC Name 2,3,3,5,6-pentahydroxy-2-phenylchromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H12O7/c16-9-6-7-10-11(12(9)17)13(18)14(19,20)15(21,22-10)8-4-2-1-3-5-8/h1-7,16-17,19-21H
InChI Key QJMWNZIONUJUHA-UHFFFAOYSA-N
Popularity 54 references in papers

Physical and Chemical Properties

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Molecular Formula C15H12O7
Molecular Weight 304.25 g/mol
Exact Mass 304.05830272 g/mol
Topological Polar Surface Area (TPSA) 127.00 Ų
XlogP 0.70
Atomic LogP (AlogP) 0.20
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 1

Synonyms

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SCHEMBL30658588

2D Structure

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2D Structure of 2,3,3,5,6-Pentahydroxy-2-phenylchromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8683 86.83%
Caco-2 - 0.9532 95.32%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.7553 75.53%
OATP2B1 inhibitior - 0.7075 70.75%
OATP1B1 inhibitior + 0.9225 92.25%
OATP1B3 inhibitior + 0.9569 95.69%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8635 86.35%
P-glycoprotein inhibitior - 0.8716 87.16%
P-glycoprotein substrate - 0.9749 97.49%
CYP3A4 substrate - 0.6061 60.61%
CYP2C9 substrate - 0.8148 81.48%
CYP2D6 substrate - 0.8395 83.95%
CYP3A4 inhibition - 0.8303 83.03%
CYP2C9 inhibition - 0.5089 50.89%
CYP2C19 inhibition - 0.7957 79.57%
CYP2D6 inhibition - 0.9554 95.54%
CYP1A2 inhibition - 0.7725 77.25%
CYP2C8 inhibition - 0.7225 72.25%
CYP inhibitory promiscuity - 0.8743 87.43%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6204 62.04%
Eye corrosion - 0.9901 99.01%
Eye irritation + 0.8373 83.73%
Skin irritation + 0.5402 54.02%
Skin corrosion - 0.9567 95.67%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9516 95.16%
Micronuclear + 0.9100 91.00%
Hepatotoxicity + 0.5464 54.64%
skin sensitisation - 0.8481 84.81%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity + 0.5737 57.37%
Acute Oral Toxicity (c) II 0.5937 59.37%
Estrogen receptor binding + 0.7531 75.31%
Androgen receptor binding + 0.7780 77.80%
Thyroid receptor binding + 0.6325 63.25%
Glucocorticoid receptor binding + 0.8083 80.83%
Aromatase binding + 0.8680 86.80%
PPAR gamma + 0.8666 86.66%
Honey bee toxicity - 0.9526 95.26%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9595 95.95%

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 99.35% 91.11%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 97.18% 94.62%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 94.23% 94.08%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.89% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.61% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.54% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.06% 99.15%
CHEMBL1951 P21397 Monoamine oxidase A 86.00% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.97% 94.45%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 83.76% 94.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.62% 89.00%
CHEMBL4208 P20618 Proteasome component C5 82.02% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.11% 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.
Scutellaria baicalensis

Cross-Links

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PubChem 54231395
LOTUS LTS0181619
wikiData Q105222765