2,5-Dihydroxy-6-(hydroxymethyl)-1,3-dimethoxyanthracene-9,10-dione

Details

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Internal ID fd40a619-01c6-4625-aed9-21b1b041e51a
Taxonomy Benzenoids > Anthracenes > Anthraquinones > Hydroxyanthraquinones
IUPAC Name 2,5-dihydroxy-6-(hydroxymethyl)-1,3-dimethoxyanthracene-9,10-dione
SMILES (Canonical) COC1=C(C(=C2C(=C1)C(=O)C3=C(C2=O)C=CC(=C3O)CO)OC)O
SMILES (Isomeric) COC1=C(C(=C2C(=C1)C(=O)C3=C(C2=O)C=CC(=C3O)CO)OC)O
InChI InChI=1S/C17H14O7/c1-23-10-5-9-12(17(24-2)16(10)22)14(20)8-4-3-7(6-18)13(19)11(8)15(9)21/h3-5,18-19,22H,6H2,1-2H3
InChI Key CIYBOVCTYRLLSS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H14O7
Molecular Weight 330.29 g/mol
Exact Mass 330.07395278 g/mol
Topological Polar Surface Area (TPSA) 113.00 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.38
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,5-Dihydroxy-6-(hydroxymethyl)-1,3-dimethoxyanthracene-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 + 0.9685 96.85%
Caco-2 + 0.5962 59.62%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.6324 63.24%
OATP2B1 inhibitior - 0.5678 56.78%
OATP1B1 inhibitior + 0.9014 90.14%
OATP1B3 inhibitior + 0.8881 88.81%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.6765 67.65%
P-glycoprotein inhibitior - 0.7543 75.43%
P-glycoprotein substrate - 0.7980 79.80%
CYP3A4 substrate + 0.5457 54.57%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7944 79.44%
CYP3A4 inhibition - 0.7509 75.09%
CYP2C9 inhibition - 0.5433 54.33%
CYP2C19 inhibition - 0.6618 66.18%
CYP2D6 inhibition - 0.8773 87.73%
CYP1A2 inhibition + 0.8032 80.32%
CYP2C8 inhibition + 0.4642 46.42%
CYP inhibitory promiscuity - 0.6104 61.04%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8975 89.75%
Carcinogenicity (trinary) Non-required 0.7312 73.12%
Eye corrosion - 0.9860 98.60%
Eye irritation + 0.7214 72.14%
Skin irritation - 0.7630 76.30%
Skin corrosion - 0.9443 94.43%
Ames mutagenesis + 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7799 77.99%
Micronuclear + 0.5859 58.59%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.8105 81.05%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.7640 76.40%
Acute Oral Toxicity (c) III 0.6558 65.58%
Estrogen receptor binding + 0.8922 89.22%
Androgen receptor binding - 0.5000 50.00%
Thyroid receptor binding - 0.5509 55.09%
Glucocorticoid receptor binding + 0.8210 82.10%
Aromatase binding + 0.6830 68.30%
PPAR gamma + 0.7221 72.21%
Honey bee toxicity - 0.9025 90.25%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6549 65.49%
Fish aquatic toxicity + 0.9394 93.94%

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 98.47% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.52% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.08% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.79% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.81% 89.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.58% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.41% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.47% 86.33%
CHEMBL2535 P11166 Glucose transporter 86.87% 98.75%
CHEMBL4208 P20618 Proteasome component C5 84.85% 90.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.80% 96.67%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.84% 99.17%
CHEMBL1255126 O15151 Protein Mdm4 82.35% 90.20%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.57% 85.14%
CHEMBL1951 P21397 Monoamine oxidase A 81.49% 91.49%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.50% 99.15%
CHEMBL3401 O75469 Pregnane X receptor 80.47% 94.73%

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.
Galium sinaicum

Cross-Links

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PubChem 10616395
LOTUS LTS0083289
wikiData Q104960632