Graphislactone H

Details

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Internal ID cd594949-3ed1-4e02-877d-cfb3382b61cd
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 7-hydroxy-3,4,9-trimethoxy-1-methylbenzo[c]chromen-6-one
SMILES (Canonical) CC1=CC(=C(C2=C1C3=C(C(=CC(=C3)OC)O)C(=O)O2)OC)OC
SMILES (Isomeric) CC1=CC(=C(C2=C1C3=C(C(=CC(=C3)OC)O)C(=O)O2)OC)OC
InChI InChI=1S/C17H16O6/c1-8-5-12(21-3)15(22-4)16-13(8)10-6-9(20-2)7-11(18)14(10)17(19)23-16/h5-7,18H,1-4H3
InChI Key ZKPINXURUNKUFT-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 3.50
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 H

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 + 0.8642 86.42%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6514 65.14%
OATP2B1 inhibitior - 0.8597 85.97%
OATP1B1 inhibitior + 0.9493 94.93%
OATP1B3 inhibitior + 0.9611 96.11%
MATE1 inhibitior - 0.6800 68.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.5539 55.39%
P-glycoprotein inhibitior - 0.5844 58.44%
P-glycoprotein substrate - 0.8903 89.03%
CYP3A4 substrate + 0.5206 52.06%
CYP2C9 substrate - 0.5374 53.74%
CYP2D6 substrate - 0.8728 87.28%
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 + 0.5305 53.05%
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 + 0.8025 80.25%
Skin irritation - 0.6961 69.61%
Skin corrosion - 0.9873 98.73%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6632 66.32%
Micronuclear + 0.8459 84.59%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.9463 94.63%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7731 77.31%
Acute Oral Toxicity (c) II 0.6827 68.27%
Estrogen receptor binding + 0.7423 74.23%
Androgen receptor binding - 0.4940 49.40%
Thyroid receptor binding + 0.7410 74.10%
Glucocorticoid receptor binding + 0.7810 78.10%
Aromatase binding + 0.7011 70.11%
PPAR gamma + 0.7476 74.76%
Honey bee toxicity - 0.8603 86.03%
Biodegradation - 0.8000 80.00%
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 98.37% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.41% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.99% 94.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.83% 99.15%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.28% 85.14%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 90.36% 93.65%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.04% 89.00%
CHEMBL2535 P11166 Glucose transporter 89.64% 98.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.40% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.79% 99.23%
CHEMBL3401 O75469 Pregnane X receptor 86.68% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.17% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.20% 93.99%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.42% 95.50%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.17% 94.45%
CHEMBL4208 P20618 Proteasome component C5 81.36% 90.00%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 80.00% 92.68%

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.
Inula helenium
Pinellia pedatisecta

Cross-Links

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PubChem 11529770
NPASS NPC27293
LOTUS LTS0056962
wikiData Q104202495