2,8-Dihydroxy-1-(hydroxymethyl)anthracene-9,10-dione

Details

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Internal ID 048a6c74-be2d-4d8d-afa4-2b381258a530
Taxonomy Benzenoids > Anthracenes > Anthraquinones > Hydroxyanthraquinones
IUPAC Name 2,8-dihydroxy-1-(hydroxymethyl)anthracene-9,10-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H10O5/c16-6-9-10(17)5-4-8-12(9)15(20)13-7(14(8)19)2-1-3-11(13)18/h1-5,16-18H,6H2
InChI Key YNKDPCKPMPOEAQ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H10O5
Molecular Weight 270.24 g/mol
Exact Mass 270.05282342 g/mol
Topological Polar Surface Area (TPSA) 94.80 Ų
XlogP 2.40
Atomic LogP (AlogP) 1.37
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,8-Dihydroxy-1-(hydroxymethyl)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 + 0.9764 97.64%
Caco-2 - 0.7129 71.29%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.7419 74.19%
OATP2B1 inhibitior - 0.6949 69.49%
OATP1B1 inhibitior + 0.8885 88.85%
OATP1B3 inhibitior + 0.8486 84.86%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7791 77.91%
P-glycoprotein inhibitior - 0.9406 94.06%
P-glycoprotein substrate - 0.8875 88.75%
CYP3A4 substrate - 0.6046 60.46%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8175 81.75%
CYP3A4 inhibition - 0.8474 84.74%
CYP2C9 inhibition - 0.6783 67.83%
CYP2C19 inhibition - 0.6161 61.61%
CYP2D6 inhibition - 0.9034 90.34%
CYP1A2 inhibition + 0.6838 68.38%
CYP2C8 inhibition - 0.9083 90.83%
CYP inhibitory promiscuity - 0.6516 65.16%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8485 84.85%
Carcinogenicity (trinary) Non-required 0.7041 70.41%
Eye corrosion - 0.9924 99.24%
Eye irritation + 0.9597 95.97%
Skin irritation - 0.5713 57.13%
Skin corrosion - 0.9650 96.50%
Ames mutagenesis + 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7997 79.97%
Micronuclear + 0.5959 59.59%
Hepatotoxicity + 0.6802 68.02%
skin sensitisation - 0.6969 69.69%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.7515 75.15%
Acute Oral Toxicity (c) III 0.5421 54.21%
Estrogen receptor binding + 0.8883 88.83%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.5583 55.83%
Glucocorticoid receptor binding + 0.9404 94.04%
Aromatase binding + 0.7295 72.95%
PPAR gamma + 0.8755 87.55%
Honey bee toxicity - 0.9383 93.83%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9686 96.86%

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 97.89% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.16% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.93% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 93.29% 91.49%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.29% 99.15%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.00% 99.23%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 85.19% 96.67%
CHEMBL3401 O75469 Pregnane X receptor 83.22% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.84% 89.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.11% 96.95%

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 163013290
LOTUS LTS0041794
wikiData Q105350978