[8-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl] hydrogen sulfate

Details

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Internal ID f1836c7b-a25c-49f8-b33e-179217d1f3c3
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Biflavonoids and polyflavonoids
IUPAC Name [8-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl] hydrogen sulfate
SMILES (Canonical) C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)OS(=O)(=O)O)O
SMILES (Isomeric) C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)OS(=O)(=O)O)O
InChI InChI=1S/C30H20O13S/c31-15-5-1-13(2-6-15)21-11-19(35)24-20(36)12-23(43-44(38,39)40)26(30(24)41-21)27-28(37)25-18(34)9-17(33)10-22(25)42-29(27)14-3-7-16(32)8-4-14/h1-12,27,29,31-34,36H,(H,38,39,40)
InChI Key IPZCFPAXWINQCA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H20O13S
Molecular Weight 620.50 g/mol
Exact Mass 620.06246186 g/mol
Topological Polar Surface Area (TPSA) 226.00 Ų
XlogP 4.20
Atomic LogP (AlogP) 4.27
H-Bond Acceptor 12
H-Bond Donor 6
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [8-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl] hydrogen sulfate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7976 79.76%
Caco-2 - 0.8753 87.53%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.5315 53.15%
OATP2B1 inhibitior - 0.5566 55.66%
OATP1B1 inhibitior + 0.8442 84.42%
OATP1B3 inhibitior + 0.9290 92.90%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.4517 45.17%
P-glycoprotein inhibitior + 0.7085 70.85%
P-glycoprotein substrate - 0.6466 64.66%
CYP3A4 substrate + 0.6565 65.65%
CYP2C9 substrate + 0.6014 60.14%
CYP2D6 substrate - 0.8294 82.94%
CYP3A4 inhibition - 0.8421 84.21%
CYP2C9 inhibition - 0.7355 73.55%
CYP2C19 inhibition - 0.8080 80.80%
CYP2D6 inhibition - 0.8904 89.04%
CYP1A2 inhibition - 0.6321 63.21%
CYP2C8 inhibition + 0.8601 86.01%
CYP inhibitory promiscuity - 0.6843 68.43%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) + 0.5188 51.88%
Carcinogenicity (trinary) Non-required 0.6679 66.79%
Eye corrosion - 0.9333 93.33%
Eye irritation - 0.7326 73.26%
Skin irritation - 0.7494 74.94%
Skin corrosion - 0.8343 83.43%
Ames mutagenesis + 0.5746 57.46%
Human Ether-a-go-go-Related Gene inhibition + 0.7241 72.41%
Micronuclear + 0.9200 92.00%
Hepatotoxicity - 0.6091 60.91%
skin sensitisation - 0.8521 85.21%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.5669 56.69%
Acute Oral Toxicity (c) III 0.6211 62.11%
Estrogen receptor binding + 0.7507 75.07%
Androgen receptor binding + 0.8826 88.26%
Thyroid receptor binding + 0.5404 54.04%
Glucocorticoid receptor binding + 0.6483 64.83%
Aromatase binding - 0.6673 66.73%
PPAR gamma + 0.6855 68.55%
Honey bee toxicity - 0.6896 68.96%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9831 98.31%

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
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.94% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.79% 94.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.25% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.94% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.41% 99.15%
CHEMBL3194 P02766 Transthyretin 93.74% 90.71%
CHEMBL2581 P07339 Cathepsin D 92.19% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.89% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 89.40% 94.73%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 88.32% 95.78%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.16% 94.45%
CHEMBL308 P06493 Cyclin-dependent kinase 1 87.55% 91.73%
CHEMBL242 Q92731 Estrogen receptor beta 86.71% 98.35%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.40% 86.33%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 85.75% 86.92%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.50% 97.09%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.08% 97.14%
CHEMBL2803 P43403 Tyrosine-protein kinase ZAP-70 80.77% 82.50%
CHEMBL4530 P00488 Coagulation factor XIII 80.24% 96.00%
CHEMBL3038469 P24941 CDK2/Cyclin A 80.13% 91.38%

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.
Garcinia madruno

Cross-Links

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PubChem 162997867
LOTUS LTS0224988
wikiData Q105117605