2-Hydroxy-3-methoxy-7,8-methylenedioxy-4,9-dioxapyrene-5,10-dione

Details

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Internal ID a3a55215-a485-425e-af7c-0fcb588139cb
Taxonomy Phenylpropanoids and polyketides > Tannins > Hydrolyzable tannins
IUPAC Name 13-hydroxy-12-methoxy-3,5,10,17-tetraoxapentacyclo[9.6.2.02,6.08,18.015,19]nonadeca-1(18),2(6),7,11(19),12,14-hexaene-9,16-dione
SMILES (Canonical) COC1=C(C=C2C3=C1OC(=O)C4=CC5=C(C(=C43)OC2=O)OCO5)O
SMILES (Isomeric) COC1=C(C=C2C3=C1OC(=O)C4=CC5=C(C(=C43)OC2=O)OCO5)O
InChI InChI=1S/C16H8O8/c1-20-11-7(17)2-5-9-10-6(16(19)23-13(9)11)3-8-12(22-4-21-8)14(10)24-15(5)18/h2-3,17H,4H2,1H3
InChI Key MKSFEZKHACTMCV-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H8O8
Molecular Weight 328.23 g/mol
Exact Mass 328.02191721 g/mol
Topological Polar Surface Area (TPSA) 101.00 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.93
H-Bond Acceptor 8
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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2-Hydroxy-3-methoxy-7,8-methylenedioxy-4,9-dioxapyrene-5,10-dione

2D Structure

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2D Structure of 2-Hydroxy-3-methoxy-7,8-methylenedioxy-4,9-dioxapyrene-5,10-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9725 97.25%
Caco-2 + 0.6067 60.67%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7794 77.94%
OATP2B1 inhibitior - 0.7181 71.81%
OATP1B1 inhibitior + 0.9352 93.52%
OATP1B3 inhibitior + 0.9768 97.68%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.6084 60.84%
P-glycoprotein inhibitior - 0.7369 73.69%
P-glycoprotein substrate - 0.8992 89.92%
CYP3A4 substrate - 0.5190 51.90%
CYP2C9 substrate - 0.8212 82.12%
CYP2D6 substrate - 0.8357 83.57%
CYP3A4 inhibition + 0.6705 67.05%
CYP2C9 inhibition + 0.7639 76.39%
CYP2C19 inhibition + 0.6849 68.49%
CYP2D6 inhibition - 0.5363 53.63%
CYP1A2 inhibition + 0.5761 57.61%
CYP2C8 inhibition - 0.8098 80.98%
CYP inhibitory promiscuity + 0.5480 54.80%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4265 42.65%
Eye corrosion - 0.9785 97.85%
Eye irritation - 0.4837 48.37%
Skin irritation - 0.7186 71.86%
Skin corrosion - 0.9546 95.46%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4772 47.72%
Micronuclear + 0.8474 84.74%
Hepatotoxicity - 0.5302 53.02%
skin sensitisation - 0.7604 76.04%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity - 0.8605 86.05%
Acute Oral Toxicity (c) III 0.6284 62.84%
Estrogen receptor binding + 0.7044 70.44%
Androgen receptor binding + 0.5293 52.93%
Thyroid receptor binding - 0.6295 62.95%
Glucocorticoid receptor binding + 0.7690 76.90%
Aromatase binding + 0.7217 72.17%
PPAR gamma + 0.7994 79.94%
Honey bee toxicity - 0.8590 85.90%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9154 91.54%

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 99.60% 91.11%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 97.60% 96.77%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.90% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.42% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.64% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.48% 89.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 89.44% 92.62%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 89.00% 94.80%
CHEMBL2581 P07339 Cathepsin D 88.80% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.81% 99.23%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.51% 99.15%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 84.47% 80.96%
CHEMBL3401 O75469 Pregnane X receptor 83.80% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.29% 86.33%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 81.11% 98.11%
CHEMBL2535 P11166 Glucose transporter 80.74% 98.75%

Cross-Links

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PubChem 10336592
NPASS NPC237898
LOTUS LTS0164243
wikiData Q105166189