Trimethoxyanthraquinone

Details

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Internal ID db182cc3-a25c-4cb5-951d-d599cc1811ba
Taxonomy Benzenoids > Anthracenes > Anthraquinones
IUPAC Name 1,2,3-trimethoxyanthracene-9,10-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H14O5/c1-20-12-8-11-13(17(22-3)16(12)21-2)15(19)10-7-5-4-6-9(10)14(11)18/h4-8H,1-3H3
InChI Key SODIHNOHBGHBIQ-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C17H14O5
Molecular Weight 298.29 g/mol
Exact Mass 298.08412354 g/mol
Topological Polar Surface Area (TPSA) 61.80 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.49
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Trimethoxyanthraquinone

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 + 0.8440 84.40%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Mitochondria 0.7592 75.92%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9449 94.49%
OATP1B3 inhibitior + 0.9708 97.08%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.4653 46.53%
P-glycoprotein inhibitior - 0.4760 47.60%
P-glycoprotein substrate - 0.9387 93.87%
CYP3A4 substrate - 0.5351 53.51%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6800 68.00%
CYP3A4 inhibition - 0.6045 60.45%
CYP2C9 inhibition - 0.9144 91.44%
CYP2C19 inhibition - 0.8482 84.82%
CYP2D6 inhibition - 0.9480 94.80%
CYP1A2 inhibition + 0.9743 97.43%
CYP2C8 inhibition - 0.7552 75.52%
CYP inhibitory promiscuity - 0.5249 52.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8995 89.95%
Carcinogenicity (trinary) Non-required 0.5057 50.57%
Eye corrosion - 0.9741 97.41%
Eye irritation + 0.9255 92.55%
Skin irritation - 0.7642 76.42%
Skin corrosion - 0.9789 97.89%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4904 49.04%
Micronuclear + 0.6659 66.59%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.9136 91.36%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.6299 62.99%
Acute Oral Toxicity (c) II 0.5137 51.37%
Estrogen receptor binding + 0.8207 82.07%
Androgen receptor binding + 0.6455 64.55%
Thyroid receptor binding + 0.5823 58.23%
Glucocorticoid receptor binding + 0.6952 69.52%
Aromatase binding + 0.5550 55.50%
PPAR gamma + 0.5639 56.39%
Honey bee toxicity - 0.8077 80.77%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9835 98.35%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.15% 95.56%
CHEMBL2581 P07339 Cathepsin D 95.98% 98.95%
CHEMBL2535 P11166 Glucose transporter 93.44% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.75% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.72% 86.33%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 89.04% 82.69%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.89% 96.09%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 87.07% 96.67%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.70% 91.11%
CHEMBL1907 P15144 Aminopeptidase N 82.99% 93.31%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.71% 97.14%
CHEMBL4247 Q9UM73 ALK tyrosine kinase receptor 82.67% 96.86%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.44% 89.00%
CHEMBL1255126 O15151 Protein Mdm4 81.39% 90.20%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 81.18% 94.03%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.72% 99.23%

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.
Oldenlandia umbellata

Cross-Links

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PubChem 12697029
LOTUS LTS0237242
wikiData Q105256867