9-(1,3-benzodioxol-5-yl)-4,5,6,7-tetramethoxy-3H-benzo[f][2]benzofuran-1-one

Details

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Internal ID dcbca09c-be93-4c1a-a4f9-15ba5354ce2b
Taxonomy Lignans, neolignans and related compounds > Arylnaphthalene lignans
IUPAC Name 9-(1,3-benzodioxol-5-yl)-4,5,6,7-tetramethoxy-3H-benzo[f][2]benzofuran-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H20O8/c1-25-16-8-12-17(11-5-6-14-15(7-11)31-10-30-14)18-13(9-29-23(18)24)20(26-2)19(12)22(28-4)21(16)27-3/h5-8H,9-10H2,1-4H3
InChI Key JZLOANXPTOXARG-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H20O8
Molecular Weight 424.40 g/mol
Exact Mass 424.11581759 g/mol
Topological Polar Surface Area (TPSA) 81.70 Ų
XlogP 3.90
Atomic LogP (AlogP) 3.94
H-Bond Acceptor 8
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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SCHEMBL4051601
AKOS040763347
205505-62-0
9-(1,3-benzodioxol-5-yl)-4,5,6,7-tetramethoxy-3H-benzo[f][2]benzofuran-1-one

2D Structure

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2D Structure of 9-(1,3-benzodioxol-5-yl)-4,5,6,7-tetramethoxy-3H-benzo[f][2]benzofuran-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9887 98.87%
Caco-2 + 0.8919 89.19%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6974 69.74%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9397 93.97%
OATP1B3 inhibitior + 0.9651 96.51%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.9408 94.08%
P-glycoprotein inhibitior + 0.7183 71.83%
P-glycoprotein substrate - 0.8524 85.24%
CYP3A4 substrate + 0.5801 58.01%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8360 83.60%
CYP3A4 inhibition + 0.8826 88.26%
CYP2C9 inhibition + 0.9061 90.61%
CYP2C19 inhibition + 0.9355 93.55%
CYP2D6 inhibition - 0.7937 79.37%
CYP1A2 inhibition - 0.6855 68.55%
CYP2C8 inhibition + 0.5928 59.28%
CYP inhibitory promiscuity + 0.9414 94.14%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.3969 39.69%
Eye corrosion - 0.9851 98.51%
Eye irritation - 0.6866 68.66%
Skin irritation - 0.8278 82.78%
Skin corrosion - 0.9689 96.89%
Ames mutagenesis + 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6937 69.37%
Micronuclear + 0.7400 74.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.6964 69.64%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.4578 45.78%
Acute Oral Toxicity (c) III 0.4888 48.88%
Estrogen receptor binding + 0.8962 89.62%
Androgen receptor binding + 0.6485 64.85%
Thyroid receptor binding + 0.7678 76.78%
Glucocorticoid receptor binding + 0.9181 91.81%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.7626 76.26%
Honey bee toxicity - 0.7688 76.88%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity + 0.9693 96.93%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.29% 94.45%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 98.14% 96.77%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.61% 91.11%
CHEMBL240 Q12809 HERG 96.25% 89.76%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.05% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.31% 95.56%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 94.96% 94.80%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 92.73% 92.62%
CHEMBL2581 P07339 Cathepsin D 92.38% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.19% 89.00%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 91.97% 80.96%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.26% 94.00%
CHEMBL1907 P15144 Aminopeptidase N 89.90% 93.31%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.58% 85.14%
CHEMBL2535 P11166 Glucose transporter 89.25% 98.75%
CHEMBL4940 P07195 L-lactate dehydrogenase B chain 87.07% 95.53%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.31% 96.09%
CHEMBL2717 Q9HCR9 Phosphodiesterase 11A 85.57% 85.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.42% 97.14%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.60% 96.00%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 82.09% 98.21%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 81.40% 95.78%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 80.72% 92.38%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 80.54% 94.03%

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.
Protium unifoliolatum

Cross-Links

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PubChem 10670001
LOTUS LTS0073645
wikiData Q105137466