8-Hydroxy-1,2,3,5-tetramethoxy-6-methylanthracene-9,10-dione

Details

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Internal ID 3f23b79d-27fc-4040-b419-53f71891d927
Taxonomy Benzenoids > Anthracenes > Anthraquinones
IUPAC Name 8-hydroxy-1,2,3,5-tetramethoxy-6-methylanthracene-9,10-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H18O7/c1-8-6-10(20)13-14(17(8)24-3)15(21)9-7-11(23-2)18(25-4)19(26-5)12(9)16(13)22/h6-7,20H,1-5H3
InChI Key ZEHCTIWURTZYHV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H18O7
Molecular Weight 358.30 g/mol
Exact Mass 358.10525291 g/mol
Topological Polar Surface Area (TPSA) 91.30 Ų
XlogP 3.30
Atomic LogP (AlogP) 2.51
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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CHEMBL1997256
NSC-676833
NCI60_027280

2D Structure

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2D Structure of 8-Hydroxy-1,2,3,5-tetramethoxy-6-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 + 0.9917 99.17%
Caco-2 + 0.7840 78.40%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.8123 81.23%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9381 93.81%
OATP1B3 inhibitior + 0.9073 90.73%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.6899 68.99%
P-glycoprotein inhibitior - 0.6387 63.87%
P-glycoprotein substrate - 0.9105 91.05%
CYP3A4 substrate + 0.5000 50.00%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7976 79.76%
CYP3A4 inhibition - 0.7693 76.93%
CYP2C9 inhibition - 0.9504 95.04%
CYP2C19 inhibition - 0.9033 90.33%
CYP2D6 inhibition - 0.8995 89.95%
CYP1A2 inhibition + 0.9180 91.80%
CYP2C8 inhibition - 0.6097 60.97%
CYP inhibitory promiscuity - 0.7790 77.90%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8995 89.95%
Carcinogenicity (trinary) Non-required 0.5370 53.70%
Eye corrosion - 0.9825 98.25%
Eye irritation + 0.7767 77.67%
Skin irritation - 0.6825 68.25%
Skin corrosion - 0.9777 97.77%
Ames mutagenesis + 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6908 69.08%
Micronuclear + 0.7259 72.59%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.9226 92.26%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.5466 54.66%
Acute Oral Toxicity (c) II 0.6288 62.88%
Estrogen receptor binding + 0.8523 85.23%
Androgen receptor binding - 0.6885 68.85%
Thyroid receptor binding + 0.5933 59.33%
Glucocorticoid receptor binding + 0.6399 63.99%
Aromatase binding + 0.6587 65.87%
PPAR gamma + 0.6598 65.98%
Honey bee toxicity - 0.8837 88.37%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9767 97.67%

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 95.44% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.40% 91.11%
CHEMBL2581 P07339 Cathepsin D 89.82% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.35% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.74% 99.23%
CHEMBL2535 P11166 Glucose transporter 88.03% 98.75%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.75% 99.15%
CHEMBL4208 P20618 Proteasome component C5 86.99% 90.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.98% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.49% 89.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 83.48% 93.40%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.22% 96.00%
CHEMBL4247 Q9UM73 ALK tyrosine kinase receptor 82.14% 96.86%
CHEMBL1937 Q92769 Histone deacetylase 2 81.52% 94.75%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.13% 96.67%

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 385561
LOTUS LTS0257659
wikiData Q105373246