1,2,4,5,8-Pentahydroxy-7-methylanthracene-9,10-dione

Details

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Internal ID 6f17e1e3-5ace-4890-9ac4-569fec638ca2
Taxonomy Benzenoids > Anthracenes > Anthraquinones > Hydroxyanthraquinones
IUPAC Name 1,2,4,5,8-pentahydroxy-7-methylanthracene-9,10-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H10O7/c1-4-2-5(16)8-10(12(4)19)15(22)11-9(14(8)21)6(17)3-7(18)13(11)20/h2-3,16-20H,1H3
InChI Key AXEZGFOGSXQCPB-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H10O7
Molecular Weight 302.23 g/mol
Exact Mass 302.04265265 g/mol
Topological Polar Surface Area (TPSA) 135.00 Ų
XlogP 2.60
Atomic LogP (AlogP) 1.30
H-Bond Acceptor 7
H-Bond Donor 5
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,2,4,5,8-Pentahydroxy-7-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 + 0.9566 95.66%
Caco-2 - 0.7028 70.28%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.7001 70.01%
OATP2B1 inhibitior - 0.6837 68.37%
OATP1B1 inhibitior + 0.9361 93.61%
OATP1B3 inhibitior + 0.9563 95.63%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9208 92.08%
P-glycoprotein inhibitior - 0.9407 94.07%
P-glycoprotein substrate - 0.9754 97.54%
CYP3A4 substrate - 0.6814 68.14%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8352 83.52%
CYP3A4 inhibition - 0.7915 79.15%
CYP2C9 inhibition + 0.5205 52.05%
CYP2C19 inhibition - 0.9391 93.91%
CYP2D6 inhibition - 0.8513 85.13%
CYP1A2 inhibition + 0.8546 85.46%
CYP2C8 inhibition - 0.9463 94.63%
CYP inhibitory promiscuity - 0.7651 76.51%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8775 87.75%
Carcinogenicity (trinary) Non-required 0.5492 54.92%
Eye corrosion - 0.9910 99.10%
Eye irritation + 0.8239 82.39%
Skin irritation + 0.6662 66.62%
Skin corrosion - 0.6358 63.58%
Ames mutagenesis + 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7104 71.04%
Micronuclear + 0.8200 82.00%
Hepatotoxicity + 0.7680 76.80%
skin sensitisation - 0.5647 56.47%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.5176 51.76%
Acute Oral Toxicity (c) III 0.6791 67.91%
Estrogen receptor binding + 0.7457 74.57%
Androgen receptor binding + 0.6292 62.92%
Thyroid receptor binding - 0.7213 72.13%
Glucocorticoid receptor binding + 0.8878 88.78%
Aromatase binding - 0.5051 50.51%
PPAR gamma + 0.6815 68.15%
Honey bee toxicity - 0.9735 97.35%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9828 98.28%

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 96.38% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.57% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 90.67% 94.73%
CHEMBL2581 P07339 Cathepsin D 89.25% 98.95%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 85.75% 93.40%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.86% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.54% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.47% 94.00%
CHEMBL4208 P20618 Proteasome component C5 82.12% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.37% 99.23%

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 85990596
LOTUS LTS0129267
wikiData Q104920504