Bryaquinone

Details

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Internal ID 30a81094-c476-4b20-890f-661da381ad65
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans
IUPAC Name 4-hydroxy-3,7-dimethoxy-6H-[1]benzofuro[3,2-c]chromene-9,10-dione
SMILES (Canonical) COC1=C(C2=C(C=C1)C3=C(CO2)C4=C(O3)C(=O)C(=O)C=C4OC)O
SMILES (Isomeric) COC1=C(C2=C(C=C1)C3=C(CO2)C4=C(O3)C(=O)C(=O)C=C4OC)O
InChI InChI=1S/C17H12O7/c1-21-10-4-3-7-15-8(6-23-16(7)14(10)20)12-11(22-2)5-9(18)13(19)17(12)24-15/h3-5,20H,6H2,1-2H3
InChI Key GRCODZNXJRUTGU-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H12O7
Molecular Weight 328.27 g/mol
Exact Mass 328.05830272 g/mol
Topological Polar Surface Area (TPSA) 95.20 Ų
XlogP 1.40
Atomic LogP (AlogP) 2.31
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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LMPK12070143

2D Structure

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2D Structure of Bryaquinone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9780 97.80%
Caco-2 + 0.7253 72.53%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.8196 81.96%
OATP2B1 inhibitior - 0.7185 71.85%
OATP1B1 inhibitior + 0.9284 92.84%
OATP1B3 inhibitior + 0.9713 97.13%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5128 51.28%
P-glycoprotein inhibitior - 0.5732 57.32%
P-glycoprotein substrate - 0.6130 61.30%
CYP3A4 substrate + 0.5916 59.16%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8071 80.71%
CYP3A4 inhibition + 0.6660 66.60%
CYP2C9 inhibition + 0.7767 77.67%
CYP2C19 inhibition + 0.8731 87.31%
CYP2D6 inhibition - 0.6302 63.02%
CYP1A2 inhibition + 0.6982 69.82%
CYP2C8 inhibition + 0.5393 53.93%
CYP inhibitory promiscuity + 0.8196 81.96%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4968 49.68%
Eye corrosion - 0.9866 98.66%
Eye irritation + 0.5458 54.58%
Skin irritation - 0.7461 74.61%
Skin corrosion - 0.9580 95.80%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7140 71.40%
Micronuclear + 0.7700 77.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.6813 68.13%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.6410 64.10%
Acute Oral Toxicity (c) II 0.4595 45.95%
Estrogen receptor binding + 0.8773 87.73%
Androgen receptor binding + 0.7342 73.42%
Thyroid receptor binding - 0.6019 60.19%
Glucocorticoid receptor binding + 0.8062 80.62%
Aromatase binding + 0.6546 65.46%
PPAR gamma + 0.7117 71.17%
Honey bee toxicity - 0.7992 79.92%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6049 60.49%
Fish aquatic toxicity + 0.9657 96.57%

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
CHEMBL1951 P21397 Monoamine oxidase A 97.73% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.41% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.04% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.01% 95.56%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 92.12% 98.21%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.96% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.16% 94.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 89.00% 96.67%
CHEMBL4208 P20618 Proteasome component C5 88.64% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.51% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.97% 95.89%
CHEMBL2535 P11166 Glucose transporter 86.36% 98.75%
CHEMBL3492 P49721 Proteasome Macropain subunit 85.86% 90.24%
CHEMBL1255126 O15151 Protein Mdm4 84.93% 90.20%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.85% 96.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.09% 96.77%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.13% 93.99%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.91% 99.23%
CHEMBL3194 P02766 Transthyretin 81.08% 90.71%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 80.79% 96.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.28% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.26% 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.
Brya ebenus

Cross-Links

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PubChem 44257496
LOTUS LTS0166351
wikiData Q104250448