3,8,9-Trihydroxy-6-methoxy-3,7-dimethyl-2,4-dihydroanthracen-1-one

Details

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Internal ID 569abb4f-9f65-492d-96bf-8f1ae940e43d
Taxonomy Benzenoids > Anthracenes
IUPAC Name 3,8,9-trihydroxy-6-methoxy-3,7-dimethyl-2,4-dihydroanthracen-1-one
SMILES (Canonical) CC1=C(C2=C(C3=C(CC(CC3=O)(C)O)C=C2C=C1OC)O)O
SMILES (Isomeric) CC1=C(C2=C(C3=C(CC(CC3=O)(C)O)C=C2C=C1OC)O)O
InChI InChI=1S/C17H18O5/c1-8-12(22-3)5-9-4-10-6-17(2,21)7-11(18)13(10)16(20)14(9)15(8)19/h4-5,19-21H,6-7H2,1-3H3
InChI Key YYVFJEFIHRGYRX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H18O5
Molecular Weight 302.32 g/mol
Exact Mass 302.11542367 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.45
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 3,8,9-Trihydroxy-6-methoxy-3,7-dimethyl-2,4-dihydroanthracen-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9860 98.60%
Caco-2 + 0.8473 84.73%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7072 70.72%
OATP2B1 inhibitior - 0.8586 85.86%
OATP1B1 inhibitior + 0.8803 88.03%
OATP1B3 inhibitior + 0.9413 94.13%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8146 81.46%
P-glycoprotein inhibitior - 0.8796 87.96%
P-glycoprotein substrate - 0.7567 75.67%
CYP3A4 substrate + 0.5730 57.30%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7969 79.69%
CYP3A4 inhibition - 0.5391 53.91%
CYP2C9 inhibition - 0.8050 80.50%
CYP2C19 inhibition - 0.6386 63.86%
CYP2D6 inhibition - 0.7792 77.92%
CYP1A2 inhibition + 0.8117 81.17%
CYP2C8 inhibition - 0.6692 66.92%
CYP inhibitory promiscuity - 0.7522 75.22%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8711 87.11%
Carcinogenicity (trinary) Non-required 0.5896 58.96%
Eye corrosion - 0.9916 99.16%
Eye irritation + 0.6542 65.42%
Skin irritation - 0.7136 71.36%
Skin corrosion - 0.9343 93.43%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5174 51.74%
Micronuclear - 0.5800 58.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.8951 89.51%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.6358 63.58%
Acute Oral Toxicity (c) III 0.5790 57.90%
Estrogen receptor binding + 0.7470 74.70%
Androgen receptor binding - 0.5596 55.96%
Thyroid receptor binding + 0.5341 53.41%
Glucocorticoid receptor binding + 0.7339 73.39%
Aromatase binding + 0.7788 77.88%
PPAR gamma + 0.7893 78.93%
Honey bee toxicity - 0.8712 87.12%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9752 97.52%

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 98.15% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.53% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.77% 85.14%
CHEMBL1937 Q92769 Histone deacetylase 2 92.45% 94.75%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 91.85% 96.21%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.83% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.82% 86.33%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.60% 92.94%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.13% 94.45%
CHEMBL2581 P07339 Cathepsin D 88.14% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.69% 93.99%
CHEMBL4208 P20618 Proteasome component C5 86.04% 90.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 86.02% 94.42%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 85.24% 93.03%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.71% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.53% 99.23%
CHEMBL2535 P11166 Glucose transporter 83.08% 98.75%
CHEMBL4829 O00763 Acetyl-CoA carboxylase 2 82.68% 98.00%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 82.41% 92.68%
CHEMBL3714130 P46095 G-protein coupled receptor 6 81.57% 97.36%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 80.88% 91.03%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.50% 99.15%

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.
Senna occidentalis

Cross-Links

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PubChem 21770758
LOTUS LTS0056539
wikiData Q105368937