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

Details

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Internal ID 10afce48-4368-49f7-92ab-872f2e0a622e
Taxonomy Lignans, neolignans and related compounds > Arylnaphthalene lignans
IUPAC Name 7,10-dihydroxy-5-methoxy-2-methyl-9-(2,7,10-trihydroxy-4-methoxy-7-methyl-5-oxo-6,8-dihydroanthracen-1-yl)anthracene-1,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C32H26O10/c1-12-5-17(34)27-28(29(12)37)26(16-7-14(33)8-20(41-3)25(16)31(27)39)23-15-6-13-10-32(2,40)11-19(36)22(13)30(38)24(15)21(42-4)9-18(23)35/h5-9,33,35,38-40H,10-11H2,1-4H3
InChI Key DCJYEFUZKKEXHM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C32H26O10
Molecular Weight 570.50 g/mol
Exact Mass 570.15259702 g/mol
Topological Polar Surface Area (TPSA) 171.00 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.70
H-Bond Acceptor 10
H-Bond Donor 5
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 - 0.7327 73.27%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8294 82.94%
OATP2B1 inhibitior - 0.8577 85.77%
OATP1B1 inhibitior + 0.8753 87.53%
OATP1B3 inhibitior + 0.9253 92.53%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.9451 94.51%
P-glycoprotein inhibitior + 0.6473 64.73%
P-glycoprotein substrate - 0.5462 54.62%
CYP3A4 substrate + 0.6818 68.18%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8358 83.58%
CYP3A4 inhibition - 0.7167 71.67%
CYP2C9 inhibition - 0.5797 57.97%
CYP2C19 inhibition + 0.6436 64.36%
CYP2D6 inhibition - 0.8693 86.93%
CYP1A2 inhibition + 0.5220 52.20%
CYP2C8 inhibition + 0.5108 51.08%
CYP inhibitory promiscuity - 0.6171 61.71%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8568 85.68%
Carcinogenicity (trinary) Non-required 0.5255 52.55%
Eye corrosion - 0.9943 99.43%
Eye irritation - 0.7868 78.68%
Skin irritation - 0.7579 75.79%
Skin corrosion - 0.9550 95.50%
Ames mutagenesis + 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6921 69.21%
Micronuclear + 0.5200 52.00%
Hepatotoxicity - 0.5695 56.95%
skin sensitisation - 0.8374 83.74%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity + 0.4734 47.34%
Acute Oral Toxicity (c) III 0.3363 33.63%
Estrogen receptor binding + 0.8562 85.62%
Androgen receptor binding + 0.6311 63.11%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.7794 77.94%
Aromatase binding + 0.6448 64.48%
PPAR gamma + 0.6854 68.54%
Honey bee toxicity - 0.7592 75.92%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9968 99.68%

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 99.39% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 97.33% 94.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 97.03% 93.99%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.59% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.32% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.03% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.55% 94.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 93.27% 92.94%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.20% 89.00%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 91.67% 92.68%
CHEMBL2581 P07339 Cathepsin D 91.09% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.05% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.92% 99.23%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 89.69% 96.21%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 88.21% 91.79%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.83% 86.33%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 86.09% 96.67%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.62% 95.89%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.12% 99.15%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.75% 91.07%
CHEMBL2535 P11166 Glucose transporter 80.33% 98.75%

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.
There are no matching plants.

Cross-Links

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PubChem 14355110
LOTUS LTS0133678
wikiData Q104975441