6-Hydroxy-1-methoxy-2-methylanthracene-9,10-dione

Details

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Internal ID 8a1fcaca-c2dd-4c0b-8d71-072aeeba6b84
Taxonomy Benzenoids > Anthracenes > Anthraquinones > Hydroxyanthraquinones
IUPAC Name 6-hydroxy-1-methoxy-2-methylanthracene-9,10-dione
SMILES (Canonical) CC1=C(C2=C(C=C1)C(=O)C3=C(C2=O)C=CC(=C3)O)OC
SMILES (Isomeric) CC1=C(C2=C(C=C1)C(=O)C3=C(C2=O)C=CC(=C3)O)OC
InChI InChI=1S/C16H12O4/c1-8-3-5-11-13(16(8)20-2)15(19)10-6-4-9(17)7-12(10)14(11)18/h3-7,17H,1-2H3
InChI Key QWSAQDJMTLEQMQ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C16H12O4
Molecular Weight 268.26 g/mol
Exact Mass 268.07355886 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.48
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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228574-06-9
DTXSID70660094

2D Structure

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2D Structure of 6-Hydroxy-1-methoxy-2-methylanthracene-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 + 0.9947 99.47%
Caco-2 + 0.6966 69.66%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.8538 85.38%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9194 91.94%
OATP1B3 inhibitior + 0.9805 98.05%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.7016 70.16%
P-glycoprotein inhibitior - 0.7922 79.22%
P-glycoprotein substrate - 0.8617 86.17%
CYP3A4 substrate - 0.5225 52.25%
CYP2C9 substrate - 0.8129 81.29%
CYP2D6 substrate - 0.7222 72.22%
CYP3A4 inhibition - 0.7839 78.39%
CYP2C9 inhibition - 0.7287 72.87%
CYP2C19 inhibition - 0.7525 75.25%
CYP2D6 inhibition - 0.8490 84.90%
CYP1A2 inhibition + 0.9504 95.04%
CYP2C8 inhibition - 0.7768 77.68%
CYP inhibitory promiscuity - 0.6782 67.82%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7929 79.29%
Carcinogenicity (trinary) Non-required 0.5626 56.26%
Eye corrosion - 0.9837 98.37%
Eye irritation + 0.9118 91.18%
Skin irritation - 0.6144 61.44%
Skin corrosion - 0.9770 97.70%
Ames mutagenesis + 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7256 72.56%
Micronuclear + 0.7759 77.59%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.9513 95.13%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.4592 45.92%
Acute Oral Toxicity (c) II 0.7324 73.24%
Estrogen receptor binding + 0.8279 82.79%
Androgen receptor binding + 0.7922 79.22%
Thyroid receptor binding - 0.5596 55.96%
Glucocorticoid receptor binding + 0.7599 75.99%
Aromatase binding + 0.7706 77.06%
PPAR gamma + 0.6170 61.70%
Honey bee toxicity - 0.8992 89.92%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.9825 98.25%

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
CHEMBL2581 P07339 Cathepsin D 97.63% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.34% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.96% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.01% 99.15%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 88.82% 97.21%
CHEMBL2535 P11166 Glucose transporter 87.37% 98.75%
CHEMBL4208 P20618 Proteasome component C5 87.08% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.06% 86.33%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.85% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 83.41% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.20% 89.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.99% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.56% 94.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.72% 96.67%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.03% 96.09%

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.
Heterophyllaea pustulata
Morinda citrifolia
Morinda lucida

Cross-Links

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PubChem 44715573
LOTUS LTS0100345
wikiData Q82576928