1,4,6-Trihydroxy-8-(2'-oxohexyl)-9,10-anthraquinone

Details

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Internal ID cee37ed7-e6b9-418d-92d2-818992342ce0
Taxonomy Benzenoids > Anthracenes > Anthraquinones > Hydroxyanthraquinones
IUPAC Name 3,5,8-trihydroxy-1-(2-oxohexyl)anthracene-9,10-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H18O6/c1-2-3-4-11(21)7-10-8-12(22)9-13-16(10)20(26)18-15(24)6-5-14(23)17(18)19(13)25/h5-6,8-9,22-24H,2-4,7H2,1H3
InChI Key BFIKHMDSOKPQID-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H18O6
Molecular Weight 354.40 g/mol
Exact Mass 354.11033829 g/mol
Topological Polar Surface Area (TPSA) 112.00 Ų
XlogP 3.90
Atomic LogP (AlogP) 2.88
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,4,6-Trihydroxy-8-(2'-oxohexyl)-9,10-anthraquinone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9904 99.04%
Caco-2 - 0.6471 64.71%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7762 77.62%
OATP2B1 inhibitior + 0.5709 57.09%
OATP1B1 inhibitior + 0.8927 89.27%
OATP1B3 inhibitior + 0.9618 96.18%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.5428 54.28%
P-glycoprotein inhibitior - 0.8920 89.20%
P-glycoprotein substrate - 0.8072 80.72%
CYP3A4 substrate - 0.5260 52.60%
CYP2C9 substrate - 0.7974 79.74%
CYP2D6 substrate - 0.8037 80.37%
CYP3A4 inhibition - 0.5691 56.91%
CYP2C9 inhibition - 0.6468 64.68%
CYP2C19 inhibition - 0.6469 64.69%
CYP2D6 inhibition - 0.7785 77.85%
CYP1A2 inhibition + 0.8180 81.80%
CYP2C8 inhibition + 0.5260 52.60%
CYP inhibitory promiscuity - 0.6949 69.49%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8511 85.11%
Carcinogenicity (trinary) Non-required 0.6262 62.62%
Eye corrosion - 0.9896 98.96%
Eye irritation + 0.6422 64.22%
Skin irritation - 0.6591 65.91%
Skin corrosion - 0.8509 85.09%
Ames mutagenesis + 0.6263 62.63%
Human Ether-a-go-go-Related Gene inhibition - 0.6405 64.05%
Micronuclear - 0.8300 83.00%
Hepatotoxicity + 0.5847 58.47%
skin sensitisation - 0.9136 91.36%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.6248 62.48%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.7233 72.33%
Acute Oral Toxicity (c) III 0.7012 70.12%
Estrogen receptor binding + 0.7671 76.71%
Androgen receptor binding + 0.6870 68.70%
Thyroid receptor binding - 0.6771 67.71%
Glucocorticoid receptor binding + 0.7965 79.65%
Aromatase binding - 0.5451 54.51%
PPAR gamma + 0.8524 85.24%
Honey bee toxicity - 0.9753 97.53%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 1.0000 100.00%

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 98.76% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.82% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 92.08% 91.49%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.12% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.79% 95.56%
CHEMBL240 Q12809 HERG 90.67% 89.76%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.09% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.85% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.97% 86.33%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.70% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 85.14% 94.73%
CHEMBL4208 P20618 Proteasome component C5 84.12% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.77% 99.23%
CHEMBL1929 P47989 Xanthine dehydrogenase 81.20% 96.12%

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 139591674
LOTUS LTS0028484
wikiData Q103795531