(3R)-3,6,9-trihydroxy-8-methoxy-3-methyl-2,4-dihydroanthracen-1-one

Details

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Internal ID 13ac7fd2-ee48-42cb-871e-e95872c78f05
Taxonomy Benzenoids > Anthracenes
IUPAC Name (3R)-3,6,9-trihydroxy-8-methoxy-3-methyl-2,4-dihydroanthracen-1-one
SMILES (Canonical) CC1(CC2=CC3=CC(=CC(=C3C(=C2C(=O)C1)O)OC)O)O
SMILES (Isomeric) C[C@]1(CC2=CC3=CC(=CC(=C3C(=C2C(=O)C1)O)OC)O)O
InChI InChI=1S/C16H16O5/c1-16(20)6-9-3-8-4-10(17)5-12(21-2)14(8)15(19)13(9)11(18)7-16/h3-5,17,19-20H,6-7H2,1-2H3/t16-/m1/s1
InChI Key WCRDTBIKDNWXLR-MRXNPFEDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H16O5
Molecular Weight 288.29 g/mol
Exact Mass 288.09977361 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.14
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 (3R)-3,6,9-trihydroxy-8-methoxy-3-methyl-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 + 0.9939 99.39%
Caco-2 + 0.7699 76.99%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7977 79.77%
OATP2B1 inhibitior - 0.7150 71.50%
OATP1B1 inhibitior + 0.8973 89.73%
OATP1B3 inhibitior + 0.9700 97.00%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8339 83.39%
P-glycoprotein inhibitior - 0.8964 89.64%
P-glycoprotein substrate - 0.7661 76.61%
CYP3A4 substrate + 0.5816 58.16%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7969 79.69%
CYP3A4 inhibition - 0.6601 66.01%
CYP2C9 inhibition - 0.8106 81.06%
CYP2C19 inhibition - 0.6044 60.44%
CYP2D6 inhibition - 0.7684 76.84%
CYP1A2 inhibition + 0.7793 77.93%
CYP2C8 inhibition - 0.6582 65.82%
CYP inhibitory promiscuity - 0.8301 83.01%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8324 83.24%
Carcinogenicity (trinary) Non-required 0.5224 52.24%
Eye corrosion - 0.9919 99.19%
Eye irritation + 0.7714 77.14%
Skin irritation - 0.7161 71.61%
Skin corrosion - 0.9529 95.29%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5896 58.96%
Micronuclear - 0.5500 55.00%
Hepatotoxicity - 0.5824 58.24%
skin sensitisation - 0.9053 90.53%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.6860 68.60%
Acute Oral Toxicity (c) III 0.6262 62.62%
Estrogen receptor binding + 0.7013 70.13%
Androgen receptor binding + 0.5476 54.76%
Thyroid receptor binding - 0.5321 53.21%
Glucocorticoid receptor binding + 0.7851 78.51%
Aromatase binding + 0.7196 71.96%
PPAR gamma + 0.7955 79.55%
Honey bee toxicity - 0.8597 85.97%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5349 53.49%
Fish aquatic toxicity + 0.9642 96.42%

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 99.27% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.10% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.81% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.68% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.24% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.99% 94.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.43% 92.94%
CHEMBL2581 P07339 Cathepsin D 90.00% 98.95%
CHEMBL4208 P20618 Proteasome component C5 89.82% 90.00%
CHEMBL1937 Q92769 Histone deacetylase 2 88.88% 94.75%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 88.44% 96.21%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.80% 95.56%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 87.06% 94.42%
CHEMBL2535 P11166 Glucose transporter 84.27% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.37% 99.23%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.33% 93.99%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.47% 91.07%

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 163013927
LOTUS LTS0171375
wikiData Q105302030