3,8,9-Trihydroxy-6-methoxy-3,7-dimethyl-10-(2,5,10-trihydroxy-7-methoxy-2,6-dimethyl-4-oxo-1,3-dihydroanthracen-9-yl)-2,4-dihydroanthracen-1-one

Details

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Internal ID 6fac34bc-794a-41b7-884a-275c00665a42
Taxonomy Lignans, neolignans and related compounds > Arylnaphthalene lignans
IUPAC Name 3,8,9-trihydroxy-6-methoxy-3,7-dimethyl-10-(2,5,10-trihydroxy-7-methoxy-2,6-dimethyl-4-oxo-1,3-dihydroanthracen-9-yl)-2,4-dihydroanthracen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C34H34O10/c1-13-21(43-5)7-15-23(17-9-33(3,41)11-19(35)25(17)31(39)27(15)29(13)37)24-16-8-22(44-6)14(2)30(38)28(16)32(40)26-18(24)10-34(4,42)12-20(26)36/h7-8,37-42H,9-12H2,1-6H3
InChI Key LZBVDXHYLXHJGU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C34H34O10
Molecular Weight 602.60 g/mol
Exact Mass 602.21519728 g/mol
Topological Polar Surface Area (TPSA) 174.00 Ų
XlogP 5.00
Atomic LogP (AlogP) 4.88
H-Bond Acceptor 10
H-Bond Donor 6
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,8,9-Trihydroxy-6-methoxy-3,7-dimethyl-10-(2,5,10-trihydroxy-7-methoxy-2,6-dimethyl-4-oxo-1,3-dihydroanthracen-9-yl)-2,4-dihydroanthracen-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 + 0.9835 98.35%
Caco-2 - 0.6600 66.00%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7865 78.65%
OATP2B1 inhibitior - 0.7153 71.53%
OATP1B1 inhibitior + 0.8743 87.43%
OATP1B3 inhibitior + 0.9116 91.16%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.8885 88.85%
P-glycoprotein inhibitior + 0.6519 65.19%
P-glycoprotein substrate - 0.7297 72.97%
CYP3A4 substrate + 0.5969 59.69%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7969 79.69%
CYP3A4 inhibition - 0.6195 61.95%
CYP2C9 inhibition - 0.7827 78.27%
CYP2C19 inhibition - 0.7526 75.26%
CYP2D6 inhibition - 0.8183 81.83%
CYP1A2 inhibition + 0.6140 61.40%
CYP2C8 inhibition - 0.6503 65.03%
CYP inhibitory promiscuity - 0.8138 81.38%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8632 86.32%
Carcinogenicity (trinary) Non-required 0.5800 58.00%
Eye corrosion - 0.9928 99.28%
Eye irritation - 0.7398 73.98%
Skin irritation - 0.7622 76.22%
Skin corrosion - 0.9308 93.08%
Ames mutagenesis + 0.5736 57.36%
Human Ether-a-go-go-Related Gene inhibition + 0.6746 67.46%
Micronuclear - 0.5300 53.00%
Hepatotoxicity - 0.5852 58.52%
skin sensitisation - 0.9256 92.56%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.7980 79.80%
Acute Oral Toxicity (c) III 0.4911 49.11%
Estrogen receptor binding + 0.7666 76.66%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding + 0.5818 58.18%
Glucocorticoid receptor binding + 0.7499 74.99%
Aromatase binding + 0.8009 80.09%
PPAR gamma + 0.7218 72.18%
Honey bee toxicity - 0.8553 85.53%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9862 98.62%

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 98.88% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.68% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.68% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.46% 94.00%
CHEMBL1937 Q92769 Histone deacetylase 2 90.36% 94.75%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 90.16% 96.21%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.87% 89.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 89.51% 93.99%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.48% 92.94%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.95% 85.14%
CHEMBL2581 P07339 Cathepsin D 87.64% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.29% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.32% 96.09%
CHEMBL2535 P11166 Glucose transporter 84.05% 98.75%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 83.49% 91.79%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.91% 95.89%
CHEMBL1871 P10275 Androgen Receptor 81.28% 96.43%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 80.70% 92.68%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.67% 99.23%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.58% 94.42%

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.
Senna occidentalis

Cross-Links

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PubChem 12769730
LOTUS LTS0168355
wikiData Q105159759