1-Hydroxy-3-methoxyanthracene-9,10-dione

Details

Top
Internal ID 94a5519d-42af-4bd0-8b83-aa61a14b9f6a
Taxonomy Benzenoids > Anthracenes > Anthraquinones
IUPAC Name 1-hydroxy-3-methoxyanthracene-9,10-dione
SMILES (Canonical) COC1=CC2=C(C(=C1)O)C(=O)C3=CC=CC=C3C2=O
SMILES (Isomeric) COC1=CC2=C(C(=C1)O)C(=O)C3=CC=CC=C3C2=O
InChI InChI=1S/C15H10O4/c1-19-8-6-11-13(12(16)7-8)15(18)10-5-3-2-4-9(10)14(11)17/h2-7,16H,1H3
InChI Key LRCKMFKYRNMGRL-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H10O4
Molecular Weight 254.24 g/mol
Exact Mass 254.05790880 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 3.50
Atomic LogP (AlogP) 2.18
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

Top
20733-99-7
1-hydroxy-3-methoxyanthraquinone
SCHEMBL16227266
DTXSID00540017

2D Structure

Top
2D Structure of 1-Hydroxy-3-methoxyanthracene-9,10-dione

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.8377 83.77%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.8542 85.42%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9441 94.41%
OATP1B3 inhibitior + 0.9897 98.97%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.7173 71.73%
P-glycoprotein inhibitior - 0.7861 78.61%
P-glycoprotein substrate - 0.9799 97.99%
CYP3A4 substrate - 0.5679 56.79%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7800 78.00%
CYP3A4 inhibition - 0.7941 79.41%
CYP2C9 inhibition - 0.5699 56.99%
CYP2C19 inhibition - 0.7155 71.55%
CYP2D6 inhibition - 0.8542 85.42%
CYP1A2 inhibition + 0.9721 97.21%
CYP2C8 inhibition - 0.8311 83.11%
CYP inhibitory promiscuity - 0.7590 75.90%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7529 75.29%
Carcinogenicity (trinary) Non-required 0.4819 48.19%
Eye corrosion - 0.9771 97.71%
Eye irritation + 0.9565 95.65%
Skin irritation - 0.5515 55.15%
Skin corrosion - 0.9785 97.85%
Ames mutagenesis + 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7236 72.36%
Micronuclear + 0.7400 74.00%
Hepatotoxicity + 0.5927 59.27%
skin sensitisation - 0.9661 96.61%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.7420 74.20%
Acute Oral Toxicity (c) II 0.6994 69.94%
Estrogen receptor binding + 0.8509 85.09%
Androgen receptor binding + 0.7783 77.83%
Thyroid receptor binding + 0.5956 59.56%
Glucocorticoid receptor binding + 0.8725 87.25%
Aromatase binding + 0.7879 78.79%
PPAR gamma + 0.6605 66.05%
Honey bee toxicity - 0.8887 88.87%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9606 96.06%

Targets

Top

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 97.81% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.23% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.22% 95.56%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 96.04% 99.15%
CHEMBL1951 P21397 Monoamine oxidase A 93.72% 91.49%
CHEMBL2535 P11166 Glucose transporter 91.57% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.31% 96.09%
CHEMBL4208 P20618 Proteasome component C5 89.92% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.57% 99.23%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 89.30% 82.69%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.85% 85.14%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 84.59% 96.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.19% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 83.04% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.44% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.39% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.71% 99.17%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 80.63% 92.67%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.54% 91.07%

Plants that contains it

Top
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.
Rubia tinctorum
Rubia wallichiana

Cross-Links

Top
PubChem 13412786
LOTUS LTS0168953
wikiData Q82415873