Graphislactone B

Details

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Internal ID 006a0678-151b-4794-9bd6-27dd48343ada
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 4-hydroxy-3,7,9-trimethoxy-1-methylbenzo[c]chromen-6-one
SMILES (Canonical) CC1=CC(=C(C2=C1C3=C(C(=CC(=C3)OC)OC)C(=O)O2)O)OC
SMILES (Isomeric) CC1=CC(=C(C2=C1C3=C(C(=CC(=C3)OC)OC)C(=O)O2)O)OC
InChI InChI=1S/C17H16O6/c1-8-5-12(22-4)15(18)16-13(8)10-6-9(20-2)7-11(21-3)14(10)17(19)23-16/h5-7,18H,1-4H3
InChI Key BVOHQDQPAURBCA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H16O6
Molecular Weight 316.30 g/mol
Exact Mass 316.09468823 g/mol
Topological Polar Surface Area (TPSA) 74.20 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.99
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Graphislactone B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9602 96.02%
Caco-2 + 0.8153 81.53%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6514 65.14%
OATP2B1 inhibitior - 0.8595 85.95%
OATP1B1 inhibitior + 0.9205 92.05%
OATP1B3 inhibitior + 0.9611 96.11%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.6799 67.99%
P-glycoprotein inhibitior - 0.5459 54.59%
P-glycoprotein substrate - 0.8851 88.51%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate - 0.6417 64.17%
CYP2D6 substrate - 0.8446 84.46%
CYP3A4 inhibition - 0.8520 85.20%
CYP2C9 inhibition - 0.9867 98.67%
CYP2C19 inhibition - 0.9199 91.99%
CYP2D6 inhibition - 0.9293 92.93%
CYP1A2 inhibition + 0.8260 82.60%
CYP2C8 inhibition - 0.6423 64.23%
CYP inhibitory promiscuity - 0.7249 72.49%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5526 55.26%
Eye corrosion - 0.9701 97.01%
Eye irritation + 0.7997 79.97%
Skin irritation - 0.6961 69.61%
Skin corrosion - 0.9873 98.73%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7204 72.04%
Micronuclear + 0.8459 84.59%
Hepatotoxicity + 0.5140 51.40%
skin sensitisation - 0.9463 94.63%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.8167 81.67%
Acute Oral Toxicity (c) II 0.6827 68.27%
Estrogen receptor binding + 0.7954 79.54%
Androgen receptor binding - 0.5367 53.67%
Thyroid receptor binding + 0.5973 59.73%
Glucocorticoid receptor binding + 0.7924 79.24%
Aromatase binding + 0.8057 80.57%
PPAR gamma + 0.7496 74.96%
Honey bee toxicity - 0.8801 88.01%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9186 91.86%

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 98.74% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.12% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.73% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.91% 85.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.76% 99.15%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 89.04% 93.65%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.99% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.43% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 85.37% 94.73%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 84.05% 94.42%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.90% 99.23%
CHEMBL2581 P07339 Cathepsin D 83.68% 98.95%
CHEMBL2535 P11166 Glucose transporter 83.31% 98.75%
CHEMBL1871 P10275 Androgen Receptor 82.52% 96.43%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.29% 99.17%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.86% 92.62%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.31% 95.50%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.27% 89.34%

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.
Strychnos kasengaensis

Cross-Links

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PubChem 10686868
LOTUS LTS0246937
wikiData Q104912295