8-Hydroxy-6-(hydroxymethyl)-1,2,3,5-tetramethoxyanthracene-9,10-dione

Details

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Internal ID ee41f257-22d6-4b3f-a04a-7ff71c7eb159
Taxonomy Benzenoids > Anthracenes > Anthraquinones
IUPAC Name 8-hydroxy-6-(hydroxymethyl)-1,2,3,5-tetramethoxyanthracene-9,10-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H18O8/c1-24-11-6-9-12(19(27-4)18(11)26-3)16(23)13-10(21)5-8(7-20)17(25-2)14(13)15(9)22/h5-6,20-21H,7H2,1-4H3
InChI Key XZFBINPJBBQLHQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H18O8
Molecular Weight 374.30 g/mol
Exact Mass 374.10016753 g/mol
Topological Polar Surface Area (TPSA) 112.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 1.69
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 8-Hydroxy-6-(hydroxymethyl)-1,2,3,5-tetramethoxyanthracene-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 + 0.9589 95.89%
Caco-2 + 0.7060 70.60%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.7772 77.72%
OATP2B1 inhibitior - 0.8597 85.97%
OATP1B1 inhibitior + 0.8891 88.91%
OATP1B3 inhibitior + 0.8046 80.46%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5062 50.62%
P-glycoprotein inhibitior - 0.6891 68.91%
P-glycoprotein substrate - 0.8474 84.74%
CYP3A4 substrate + 0.5359 53.59%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7944 79.44%
CYP3A4 inhibition - 0.7002 70.02%
CYP2C9 inhibition + 0.5531 55.31%
CYP2C19 inhibition - 0.5240 52.40%
CYP2D6 inhibition - 0.8538 85.38%
CYP1A2 inhibition + 0.8206 82.06%
CYP2C8 inhibition - 0.6223 62.23%
CYP inhibitory promiscuity + 0.5201 52.01%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.8863 88.63%
Carcinogenicity (trinary) Non-required 0.6675 66.75%
Eye corrosion - 0.9901 99.01%
Eye irritation - 0.4794 47.94%
Skin irritation - 0.8048 80.48%
Skin corrosion - 0.9672 96.72%
Ames mutagenesis + 0.7546 75.46%
Human Ether-a-go-go-Related Gene inhibition - 0.6825 68.25%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.8570 85.70%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.5085 50.85%
Acute Oral Toxicity (c) III 0.5801 58.01%
Estrogen receptor binding + 0.8873 88.73%
Androgen receptor binding - 0.6562 65.62%
Thyroid receptor binding + 0.5289 52.89%
Glucocorticoid receptor binding + 0.8180 81.80%
Aromatase binding + 0.7739 77.39%
PPAR gamma + 0.6321 63.21%
Honey bee toxicity - 0.8737 87.37%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6549 65.49%
Fish aquatic toxicity + 0.9548 95.48%

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 97.19% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.82% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.86% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.74% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 90.58% 94.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.80% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.12% 89.00%
CHEMBL4208 P20618 Proteasome component C5 86.82% 90.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.53% 93.99%
CHEMBL2535 P11166 Glucose transporter 85.74% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.32% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.73% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.65% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.04% 99.23%
CHEMBL1255126 O15151 Protein Mdm4 82.83% 90.20%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.74% 99.15%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.92% 86.92%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.66% 85.14%

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.
Chamaecrista greggii

Cross-Links

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PubChem 101676230
LOTUS LTS0144166
wikiData Q105344887