9-(1,3-benzodioxol-5-yl)-5-[(2R,3R,4R,5R)-3-hydroxy-4,5-dimethoxyoxan-2-yl]oxy-6H-[2]benzofuro[6,5-f][1,3]benzodioxol-8-one

Details

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Internal ID 7fe8e1fe-7646-4b1e-a78e-19cc74b0cee8
Taxonomy Lignans, neolignans and related compounds > Lignan glycosides
IUPAC Name 9-(1,3-benzodioxol-5-yl)-5-[(2R,3R,4R,5R)-3-hydroxy-4,5-dimethoxyoxan-2-yl]oxy-6H-[2]benzofuro[6,5-f][1,3]benzodioxol-8-one
SMILES (Canonical) COC1COC(C(C1OC)O)OC2=C3COC(=O)C3=C(C4=CC5=C(C=C42)OCO5)C6=CC7=C(C=C6)OCO7
SMILES (Isomeric) CO[C@@H]1CO[C@@H]([C@@H]([C@H]1OC)O)OC2=C3COC(=O)C3=C(C4=CC5=C(C=C42)OCO5)C6=CC7=C(C=C6)OCO7
InChI InChI=1S/C27H24O11/c1-30-20-9-33-27(23(28)25(20)31-2)38-24-14-7-19-18(36-11-37-19)6-13(14)21(22-15(24)8-32-26(22)29)12-3-4-16-17(5-12)35-10-34-16/h3-7,20,23,25,27-28H,8-11H2,1-2H3/t20-,23-,25+,27-/m1/s1
InChI Key ZXQBXVCLILMITL-KLZKGZPJSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C27H24O11
Molecular Weight 524.50 g/mol
Exact Mass 524.13186158 g/mol
Topological Polar Surface Area (TPSA) 120.00 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.76
H-Bond Acceptor 11
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 9-(1,3-benzodioxol-5-yl)-5-[(2R,3R,4R,5R)-3-hydroxy-4,5-dimethoxyoxan-2-yl]oxy-6H-[2]benzofuro[6,5-f][1,3]benzodioxol-8-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9542 95.42%
Caco-2 - 0.5802 58.02%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.8000 80.00%
Subcellular localzation Mitochondria 0.7384 73.84%
OATP2B1 inhibitior - 0.8651 86.51%
OATP1B1 inhibitior + 0.9176 91.76%
OATP1B3 inhibitior + 0.9409 94.09%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9759 97.59%
P-glycoprotein inhibitior + 0.7572 75.72%
P-glycoprotein substrate - 0.6543 65.43%
CYP3A4 substrate + 0.6493 64.93%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8611 86.11%
CYP3A4 inhibition + 0.7020 70.20%
CYP2C9 inhibition + 0.6310 63.10%
CYP2C19 inhibition + 0.7408 74.08%
CYP2D6 inhibition - 0.7507 75.07%
CYP1A2 inhibition - 0.8156 81.56%
CYP2C8 inhibition + 0.5121 51.21%
CYP inhibitory promiscuity + 0.7457 74.57%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5068 50.68%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.9113 91.13%
Skin irritation - 0.7923 79.23%
Skin corrosion - 0.9525 95.25%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5688 56.88%
Micronuclear + 0.5700 57.00%
Hepatotoxicity + 0.5927 59.27%
skin sensitisation - 0.8151 81.51%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.7943 79.43%
Acute Oral Toxicity (c) I 0.7557 75.57%
Estrogen receptor binding + 0.7443 74.43%
Androgen receptor binding + 0.7431 74.31%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.7298 72.98%
Aromatase binding - 0.6367 63.67%
PPAR gamma + 0.7398 73.98%
Honey bee toxicity - 0.6568 65.68%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9158 91.58%

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 99.10% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 99.00% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.35% 94.45%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 97.98% 94.80%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 97.59% 96.77%
CHEMBL2581 P07339 Cathepsin D 95.84% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.21% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.12% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 91.64% 92.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.11% 86.33%
CHEMBL4225 P49760 Dual specificity protein kinase CLK2 89.68% 80.96%
CHEMBL2039 P27338 Monoamine oxidase B 89.17% 92.51%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.89% 85.14%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.82% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.12% 100.00%
CHEMBL3922 P50579 Methionine aminopeptidase 2 86.57% 97.28%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.22% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.83% 94.00%
CHEMBL2535 P11166 Glucose transporter 83.05% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.79% 99.23%
CHEMBL1907 P15144 Aminopeptidase N 80.09% 93.31%

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.
Cleistanthus collinus

Cross-Links

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PubChem 162851728
LOTUS LTS0232710
wikiData Q105385696