7-(2,10-Dihydroxy-5,7-dimethoxy-2-methyl-4-oxo-1,3-dihydroanthracen-9-yl)-3,9-dihydroxy-6,8-dimethoxy-3-methyl-2,4-dihydroanthracen-1-one

Details

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Internal ID 76552658-a4aa-4a68-a00c-6908aa88d29e
Taxonomy Lignans, neolignans and related compounds > Arylnaphthalene lignans
IUPAC Name 7-(2,10-dihydroxy-5,7-dimethoxy-2-methyl-4-oxo-1,3-dihydroanthracen-9-yl)-3,9-dihydroxy-6,8-dimethoxy-3-methyl-2,4-dihydroanthracen-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C34H34O10/c1-33(39)11-16-7-15-8-22(42-4)29(32(44-6)25(15)30(37)24(16)20(35)13-33)26-18-9-17(41-3)10-23(43-5)28(18)31(38)27-19(26)12-34(2,40)14-21(27)36/h7-10,37-40H,11-14H2,1-6H3
InChI Key MGODXJCESXHVIE-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) 152.00 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.87
H-Bond Acceptor 10
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-(2,10-Dihydroxy-5,7-dimethoxy-2-methyl-4-oxo-1,3-dihydroanthracen-9-yl)-3,9-dihydroxy-6,8-dimethoxy-3-methyl-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 + 0.9917 99.17%
Caco-2 - 0.7227 72.27%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.8583 85.83%
OATP2B1 inhibitior - 0.8582 85.82%
OATP1B1 inhibitior + 0.8773 87.73%
OATP1B3 inhibitior + 0.9240 92.40%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9091 90.91%
P-glycoprotein inhibitior + 0.7628 76.28%
P-glycoprotein substrate - 0.5160 51.60%
CYP3A4 substrate + 0.6505 65.05%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7969 79.69%
CYP3A4 inhibition - 0.7825 78.25%
CYP2C9 inhibition - 0.8247 82.47%
CYP2C19 inhibition - 0.7575 75.75%
CYP2D6 inhibition - 0.8635 86.35%
CYP1A2 inhibition + 0.6305 63.05%
CYP2C8 inhibition + 0.5463 54.63%
CYP inhibitory promiscuity - 0.8659 86.59%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8345 83.45%
Carcinogenicity (trinary) Non-required 0.5305 53.05%
Eye corrosion - 0.9938 99.38%
Eye irritation - 0.8646 86.46%
Skin irritation - 0.7697 76.97%
Skin corrosion - 0.9482 94.82%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7373 73.73%
Micronuclear - 0.5300 53.00%
Hepatotoxicity - 0.5299 52.99%
skin sensitisation - 0.9402 94.02%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.7277 72.77%
Acute Oral Toxicity (c) III 0.4389 43.89%
Estrogen receptor binding + 0.8491 84.91%
Androgen receptor binding + 0.5231 52.31%
Thyroid receptor binding + 0.5881 58.81%
Glucocorticoid receptor binding + 0.7955 79.55%
Aromatase binding + 0.7263 72.63%
PPAR gamma + 0.7052 70.52%
Honey bee toxicity - 0.8281 82.81%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5051 50.51%
Fish aquatic toxicity + 0.9892 98.92%

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 99.70% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.04% 85.14%
CHEMBL3192 Q9BY41 Histone deacetylase 8 95.81% 93.99%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.69% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.51% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.13% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.08% 94.45%
CHEMBL2535 P11166 Glucose transporter 91.34% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.26% 96.09%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 90.39% 92.68%
CHEMBL4208 P20618 Proteasome component C5 89.45% 90.00%
CHEMBL2708 Q16584 Mitogen-activated protein kinase kinase kinase 11 89.32% 81.14%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.28% 92.94%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.15% 99.15%
CHEMBL4040 P28482 MAP kinase ERK2 87.79% 83.82%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 87.30% 91.79%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 86.15% 94.42%
CHEMBL2581 P07339 Cathepsin D 86.04% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 85.90% 94.75%
CHEMBL2056 P21728 Dopamine D1 receptor 85.00% 91.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 84.94% 96.21%
CHEMBL1907 P15144 Aminopeptidase N 84.66% 93.31%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.48% 99.23%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.97% 96.77%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.92% 92.62%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.30% 91.07%
CHEMBL4302 P08183 P-glycoprotein 1 82.31% 92.98%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.66% 95.50%

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 162953189
LOTUS LTS0260876
wikiData Q105163470