2-(Ethoxymethyl)-1,3,5-trihydroxy-6-methoxyanthracene-9,10-dione

Details

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Internal ID 79e1405d-a2e3-4923-92b1-04a18a963827
Taxonomy Benzenoids > Anthracenes > Anthraquinones > Hydroxyanthraquinones
IUPAC Name 2-(ethoxymethyl)-1,3,5-trihydroxy-6-methoxyanthracene-9,10-dione
SMILES (Canonical) CCOCC1=C(C=C2C(=C1O)C(=O)C3=C(C2=O)C(=C(C=C3)OC)O)O
SMILES (Isomeric) CCOCC1=C(C=C2C(=C1O)C(=O)C3=C(C2=O)C(=C(C=C3)OC)O)O
InChI InChI=1S/C18H16O7/c1-3-25-7-10-11(19)6-9-14(17(10)22)15(20)8-4-5-12(24-2)18(23)13(8)16(9)21/h4-6,19,22-23H,3,7H2,1-2H3
InChI Key XTXAOKFDPSACFJ-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C18H16O7
Molecular Weight 344.30 g/mol
Exact Mass 344.08960285 g/mol
Topological Polar Surface Area (TPSA) 113.00 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.12
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(Ethoxymethyl)-1,3,5-trihydroxy-6-methoxyanthracene-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 + 0.9863 98.63%
Caco-2 + 0.5193 51.93%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7076 70.76%
OATP2B1 inhibitior - 0.7052 70.52%
OATP1B1 inhibitior + 0.8745 87.45%
OATP1B3 inhibitior + 0.9353 93.53%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.5314 53.14%
P-glycoprotein inhibitior - 0.7898 78.98%
P-glycoprotein substrate - 0.7707 77.07%
CYP3A4 substrate + 0.5619 56.19%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7988 79.88%
CYP3A4 inhibition - 0.9098 90.98%
CYP2C9 inhibition + 0.5165 51.65%
CYP2C19 inhibition - 0.6299 62.99%
CYP2D6 inhibition - 0.8438 84.38%
CYP1A2 inhibition + 0.6334 63.34%
CYP2C8 inhibition + 0.6016 60.16%
CYP inhibitory promiscuity - 0.7044 70.44%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8932 89.32%
Carcinogenicity (trinary) Non-required 0.6792 67.92%
Eye corrosion - 0.9877 98.77%
Eye irritation + 0.6293 62.93%
Skin irritation - 0.7961 79.61%
Skin corrosion - 0.9445 94.45%
Ames mutagenesis + 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6178 61.78%
Micronuclear - 0.5600 56.00%
Hepatotoxicity - 0.5291 52.91%
skin sensitisation - 0.7927 79.27%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.7119 71.19%
Estrogen receptor binding + 0.9394 93.94%
Androgen receptor binding + 0.5818 58.18%
Thyroid receptor binding - 0.5320 53.20%
Glucocorticoid receptor binding + 0.8927 89.27%
Aromatase binding + 0.6489 64.89%
PPAR gamma + 0.8216 82.16%
Honey bee toxicity - 0.8853 88.53%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6649 66.49%
Fish aquatic toxicity + 0.9778 97.78%

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
CHEMBL1951 P21397 Monoamine oxidase A 97.80% 91.49%
CHEMBL2581 P07339 Cathepsin D 97.32% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.48% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.10% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.54% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.62% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.03% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.17% 86.33%
CHEMBL1255126 O15151 Protein Mdm4 86.20% 90.20%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.39% 99.17%
CHEMBL3194 P02766 Transthyretin 84.72% 90.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.37% 96.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.18% 96.67%
CHEMBL4208 P20618 Proteasome component C5 83.14% 90.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.71% 86.92%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.71% 95.89%
CHEMBL3401 O75469 Pregnane X receptor 80.52% 94.73%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.40% 90.71%

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.
Knoxia roxburghii

Cross-Links

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PubChem 91156689
NPASS NPC229944