7-Acetyl-8,9-dihydroxy-2,2,4,4,6-pentamethylanthracene-1,3-dione

Details

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Internal ID b6c1cc39-204b-41c0-9980-fd9666d4e527
Taxonomy Benzenoids > Anthracenes
IUPAC Name 7-acetyl-8,9-dihydroxy-2,2,4,4,6-pentamethylanthracene-1,3-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H22O5/c1-9-7-11-8-12-15(17(24)14(11)16(23)13(9)10(2)22)18(25)21(5,6)19(26)20(12,3)4/h7-8,23-24H,1-6H3
InChI Key MEPZRMGKLLUDEW-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C21H22O5
Molecular Weight 354.40 g/mol
Exact Mass 354.14672380 g/mol
Topological Polar Surface Area (TPSA) 91.70 Ų
XlogP 4.90
Atomic LogP (AlogP) 3.83
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Acetyl-8,9-dihydroxy-2,2,4,4,6-pentamethylanthracene-1,3-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9868 98.68%
Caco-2 + 0.6181 61.81%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8229 82.29%
OATP2B1 inhibitior - 0.7133 71.33%
OATP1B1 inhibitior + 0.7814 78.14%
OATP1B3 inhibitior + 0.8113 81.13%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8471 84.71%
P-glycoprotein inhibitior - 0.7505 75.05%
P-glycoprotein substrate - 0.8258 82.58%
CYP3A4 substrate + 0.5665 56.65%
CYP2C9 substrate - 0.7958 79.58%
CYP2D6 substrate - 0.8430 84.30%
CYP3A4 inhibition - 0.7900 79.00%
CYP2C9 inhibition + 0.5867 58.67%
CYP2C19 inhibition - 0.8396 83.96%
CYP2D6 inhibition - 0.8203 82.03%
CYP1A2 inhibition + 0.8319 83.19%
CYP2C8 inhibition - 0.5930 59.30%
CYP inhibitory promiscuity - 0.6293 62.93%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8986 89.86%
Carcinogenicity (trinary) Non-required 0.6606 66.06%
Eye corrosion - 0.9898 98.98%
Eye irritation + 0.7521 75.21%
Skin irritation - 0.6664 66.64%
Skin corrosion - 0.9200 92.00%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5842 58.42%
Micronuclear + 0.5800 58.00%
Hepatotoxicity + 0.5927 59.27%
skin sensitisation - 0.7930 79.30%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity - 0.6556 65.56%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.4707 47.07%
Acute Oral Toxicity (c) III 0.8139 81.39%
Estrogen receptor binding + 0.7351 73.51%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding + 0.5446 54.46%
Glucocorticoid receptor binding + 0.5508 55.08%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.6378 63.78%
Honey bee toxicity - 0.9242 92.42%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9924 99.24%

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 98.56% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.49% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.17% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.07% 89.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 85.74% 94.42%
CHEMBL3401 O75469 Pregnane X receptor 85.16% 94.73%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 85.01% 95.64%
CHEMBL2581 P07339 Cathepsin D 84.89% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.60% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.28% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.79% 94.00%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 82.68% 85.11%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.42% 93.03%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.11% 99.23%
CHEMBL1937 Q92769 Histone deacetylase 2 82.06% 94.75%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 23426470
LOTUS LTS0117448
wikiData Q105162361