1,8-Dihydroxy-3-methoxy-6-methyl-2-(2,3,10-trihydroxy-5,7-dimethoxy-2-methyl-4-oxo-1,3-dihydroanthracen-9-yl)anthracene-9,10-dione

Details

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Internal ID e02186a1-c7f4-4ba2-b06e-b4cbf2873bc0
Taxonomy Lignans, neolignans and related compounds > Arylnaphthalene lignans
IUPAC Name 1,8-dihydroxy-3-methoxy-6-methyl-2-(2,3,10-trihydroxy-5,7-dimethoxy-2-methyl-4-oxo-1,3-dihydroanthracen-9-yl)anthracene-9,10-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C33H28O11/c1-12-6-15-22(18(34)7-12)28(36)24-16(27(15)35)10-20(44-5)26(30(24)38)21-14-8-13(42-3)9-19(43-4)23(14)29(37)25-17(21)11-33(2,41)32(40)31(25)39/h6-10,32,34,37-38,40-41H,11H2,1-5H3
InChI Key FWOHGTUCKDNPLQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C33H28O11
Molecular Weight 600.60 g/mol
Exact Mass 600.16316171 g/mol
Topological Polar Surface Area (TPSA) 180.00 Ų
XlogP 4.80
Atomic LogP (AlogP) 3.58
H-Bond Acceptor 11
H-Bond Donor 5
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,8-Dihydroxy-3-methoxy-6-methyl-2-(2,3,10-trihydroxy-5,7-dimethoxy-2-methyl-4-oxo-1,3-dihydroanthracen-9-yl)anthracene-9,10-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9819 98.19%
Caco-2 - 0.7917 79.17%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7503 75.03%
OATP2B1 inhibitior - 0.8571 85.71%
OATP1B1 inhibitior + 0.8972 89.72%
OATP1B3 inhibitior + 0.9155 91.55%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9750 97.50%
P-glycoprotein inhibitior + 0.7391 73.91%
P-glycoprotein substrate - 0.5690 56.90%
CYP3A4 substrate + 0.6848 68.48%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8025 80.25%
CYP3A4 inhibition - 0.7097 70.97%
CYP2C9 inhibition - 0.9295 92.95%
CYP2C19 inhibition - 0.8668 86.68%
CYP2D6 inhibition - 0.9002 90.02%
CYP1A2 inhibition + 0.6408 64.08%
CYP2C8 inhibition + 0.5099 50.99%
CYP inhibitory promiscuity - 0.9588 95.88%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8932 89.32%
Carcinogenicity (trinary) Non-required 0.4948 49.48%
Eye corrosion - 0.9923 99.23%
Eye irritation - 0.8819 88.19%
Skin irritation - 0.7538 75.38%
Skin corrosion - 0.9214 92.14%
Ames mutagenesis + 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7429 74.29%
Micronuclear + 0.5300 53.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.8964 89.64%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.6413 64.13%
Acute Oral Toxicity (c) III 0.5093 50.93%
Estrogen receptor binding + 0.8325 83.25%
Androgen receptor binding + 0.6471 64.71%
Thyroid receptor binding + 0.5902 59.02%
Glucocorticoid receptor binding + 0.7681 76.81%
Aromatase binding + 0.6373 63.73%
PPAR gamma + 0.7425 74.25%
Honey bee toxicity - 0.7513 75.13%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9799 97.99%

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 99.57% 91.11%
CHEMBL240 Q12809 HERG 99.32% 89.76%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 98.32% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.95% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 95.83% 91.49%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 95.18% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.78% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 94.21% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.49% 94.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 93.20% 92.94%
CHEMBL2581 P07339 Cathepsin D 92.89% 98.95%
CHEMBL2535 P11166 Glucose transporter 89.72% 98.75%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 89.46% 91.79%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.17% 95.89%
CHEMBL340 P08684 Cytochrome P450 3A4 88.99% 91.19%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 88.64% 92.68%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.99% 85.14%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 87.96% 96.77%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 87.25% 96.21%
CHEMBL4208 P20618 Proteasome component C5 85.92% 90.00%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 85.13% 96.00%
CHEMBL2056 P21728 Dopamine D1 receptor 84.76% 91.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 84.71% 91.07%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 83.37% 91.03%
CHEMBL3438 Q05513 Protein kinase C zeta 83.35% 88.48%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.05% 96.67%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.51% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.49% 86.33%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.22% 97.14%
CHEMBL1937 Q92769 Histone deacetylase 2 81.48% 94.75%
CHEMBL4145 Q9UKV0 Histone deacetylase 9 81.24% 85.49%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.48% 100.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 85193080
LOTUS LTS0081364
wikiData Q105003452