1,3-Dihydroxy-2-(methoxymethoxy)anthracene-9,10-dione

Details

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Internal ID cbac52f0-f1e8-4b30-b349-aa7b79db5336
Taxonomy Benzenoids > Anthracenes > Anthraquinones > Hydroxyanthraquinones
IUPAC Name 1,3-dihydroxy-2-(methoxymethoxy)anthracene-9,10-dione
SMILES (Canonical) COCOC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O
SMILES (Isomeric) COCOC1=C(C=C2C(=C1O)C(=O)C3=CC=CC=C3C2=O)O
InChI InChI=1S/C16H12O6/c1-21-7-22-16-11(17)6-10-12(15(16)20)14(19)9-5-3-2-4-8(9)13(10)18/h2-6,17,20H,7H2,1H3
InChI Key JKWCMFFAFBMEMW-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H12O6
Molecular Weight 300.26 g/mol
Exact Mass 300.06338810 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 2.60
Atomic LogP (AlogP) 1.86
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,3-Dihydroxy-2-(methoxymethoxy)anthracene-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 + 0.9007 90.07%
Caco-2 - 0.5362 53.62%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.6860 68.60%
OATP2B1 inhibitior - 0.7175 71.75%
OATP1B1 inhibitior + 0.8713 87.13%
OATP1B3 inhibitior + 0.9213 92.13%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.8106 81.06%
P-glycoprotein inhibitior - 0.6106 61.06%
P-glycoprotein substrate - 0.9420 94.20%
CYP3A4 substrate + 0.5165 51.65%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8335 83.35%
CYP3A4 inhibition - 0.6056 60.56%
CYP2C9 inhibition + 0.6238 62.38%
CYP2C19 inhibition - 0.7834 78.34%
CYP2D6 inhibition - 0.7407 74.07%
CYP1A2 inhibition - 0.6173 61.73%
CYP2C8 inhibition - 0.6353 63.53%
CYP inhibitory promiscuity - 0.6327 63.27%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8975 89.75%
Carcinogenicity (trinary) Non-required 0.6247 62.47%
Eye corrosion - 0.9872 98.72%
Eye irritation + 0.8050 80.50%
Skin irritation - 0.7370 73.70%
Skin corrosion - 0.9365 93.65%
Ames mutagenesis + 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7561 75.61%
Micronuclear + 0.5833 58.33%
Hepatotoxicity + 0.6237 62.37%
skin sensitisation - 0.8546 85.46%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.5750 57.50%
Nephrotoxicity + 0.4831 48.31%
Acute Oral Toxicity (c) III 0.6382 63.82%
Estrogen receptor binding + 0.8612 86.12%
Androgen receptor binding + 0.6647 66.47%
Thyroid receptor binding - 0.5299 52.99%
Glucocorticoid receptor binding + 0.8966 89.66%
Aromatase binding + 0.6338 63.38%
PPAR gamma + 0.7843 78.43%
Honey bee toxicity - 0.9227 92.27%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9818 98.18%

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 98.41% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.25% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 97.79% 91.49%
CHEMBL2535 P11166 Glucose transporter 92.55% 98.75%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.09% 99.15%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.80% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.01% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 89.04% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.70% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.89% 86.33%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 87.24% 96.67%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.04% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.97% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.63% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.78% 96.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.73% 82.69%

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.
Galium aparine
Gynochthodes officinalis
Morinda citrifolia

Cross-Links

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PubChem 102138994
LOTUS LTS0165108
wikiData Q104402811