2-Hydroxy-1,3,4-trimethoxyanthraquinone

Details

Top
Internal ID 514d6c1a-d860-45ac-8442-399087d15aac
Taxonomy Benzenoids > Anthracenes > Anthraquinones > Hydroxyanthraquinones
IUPAC Name 2-hydroxy-1,3,4-trimethoxyanthracene-9,10-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H14O6/c1-21-15-10-11(16(22-2)17(23-3)14(15)20)13(19)9-7-5-4-6-8(9)12(10)18/h4-7,20H,1-3H3
InChI Key GNDKMLNOKPZDHG-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

Top
Molecular Formula C17H14O6
Molecular Weight 314.29 g/mol
Exact Mass 314.07903816 g/mol
Topological Polar Surface Area (TPSA) 82.10 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.19
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

Top
SCHEMBL19478231
HY-N10833
94099-63-5
2-hydroxy-1,3,4-trimethoxy-anthraquinone
CS-0637033

2D Structure

Top
2D Structure of 2-Hydroxy-1,3,4-trimethoxyanthraquinone

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 + 0.6662 66.62%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.8123 81.23%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8944 89.44%
OATP1B3 inhibitior + 0.9073 90.73%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.5853 58.53%
P-glycoprotein inhibitior - 0.6243 62.43%
P-glycoprotein substrate - 0.9729 97.29%
CYP3A4 substrate - 0.5607 56.07%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6961 69.61%
CYP3A4 inhibition - 0.7693 76.93%
CYP2C9 inhibition - 0.9504 95.04%
CYP2C19 inhibition - 0.9033 90.33%
CYP2D6 inhibition - 0.8995 89.95%
CYP1A2 inhibition + 0.9180 91.80%
CYP2C8 inhibition - 0.8540 85.40%
CYP inhibitory promiscuity - 0.7790 77.90%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8995 89.95%
Carcinogenicity (trinary) Non-required 0.5370 53.70%
Eye corrosion - 0.9825 98.25%
Eye irritation + 0.9312 93.12%
Skin irritation - 0.6825 68.25%
Skin corrosion - 0.9777 97.77%
Ames mutagenesis + 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8197 81.97%
Micronuclear + 0.7259 72.59%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.9226 92.26%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.5790 57.90%
Acute Oral Toxicity (c) II 0.6288 62.88%
Estrogen receptor binding + 0.6608 66.08%
Androgen receptor binding - 0.5590 55.90%
Thyroid receptor binding - 0.5193 51.93%
Glucocorticoid receptor binding + 0.7836 78.36%
Aromatase binding + 0.5743 57.43%
PPAR gamma + 0.5973 59.73%
Honey bee toxicity - 0.8957 89.57%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9767 97.67%

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 97.63% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.46% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.25% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.49% 99.23%
CHEMBL1951 P21397 Monoamine oxidase A 89.63% 91.49%
CHEMBL2535 P11166 Glucose transporter 87.41% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.03% 96.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 85.81% 82.69%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 85.30% 96.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.89% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.71% 96.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.95% 89.00%

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.
Cinchona calisaya
Cinchona pubescens

Cross-Links

Top
PubChem 86109348
LOTUS LTS0054628
wikiData Q105012332