1,4-Phenanthrenedione, 7-hydroxy-2,6-dimethoxy-

Details

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Internal ID 1d250d2e-12e1-4b48-9a15-a6c98d3fd939
Taxonomy Benzenoids > Phenanthrenes and derivatives > Phenanthrols
IUPAC Name 7-hydroxy-2,6-dimethoxyphenanthrene-1,4-dione
SMILES (Canonical) COC1=CC(=O)C2=C(C1=O)C=CC3=CC(=C(C=C32)OC)O
SMILES (Isomeric) COC1=CC(=O)C2=C(C1=O)C=CC3=CC(=C(C=C32)OC)O
InChI InChI=1S/C16H12O5/c1-20-13-6-10-8(5-11(13)17)3-4-9-15(10)12(18)7-14(21-2)16(9)19/h3-7,17H,1-2H3
InChI Key LWTLCLCYPAOTPO-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C16H12O5
Molecular Weight 284.26 g/mol
Exact Mass 284.06847348 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.46
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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600736-65-0
DTXSID70446572

2D Structure

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2D Structure of 1,4-Phenanthrenedione, 7-hydroxy-2,6-dimethoxy-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9959 99.59%
Caco-2 + 0.8332 83.32%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.7977 79.77%
OATP2B1 inhibitior - 0.8611 86.11%
OATP1B1 inhibitior + 0.9110 91.10%
OATP1B3 inhibitior + 0.9760 97.60%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.5494 54.94%
P-glycoprotein inhibitior - 0.8009 80.09%
P-glycoprotein substrate - 0.7659 76.59%
CYP3A4 substrate - 0.5076 50.76%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7787 77.87%
CYP3A4 inhibition - 0.5478 54.78%
CYP2C9 inhibition - 0.6162 61.62%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.7907 79.07%
CYP1A2 inhibition + 0.9209 92.09%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity + 0.6239 62.39%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8938 89.38%
Carcinogenicity (trinary) Non-required 0.5294 52.94%
Eye corrosion - 0.9878 98.78%
Eye irritation + 0.8769 87.69%
Skin irritation - 0.5939 59.39%
Skin corrosion - 0.9722 97.22%
Ames mutagenesis + 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8331 83.31%
Micronuclear + 0.7959 79.59%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.7595 75.95%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.5531 55.31%
Acute Oral Toxicity (c) II 0.6482 64.82%
Estrogen receptor binding + 0.9121 91.21%
Androgen receptor binding + 0.6651 66.51%
Thyroid receptor binding + 0.5770 57.70%
Glucocorticoid receptor binding + 0.6247 62.47%
Aromatase binding + 0.6977 69.77%
PPAR gamma + 0.7562 75.62%
Honey bee toxicity - 0.8905 89.05%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6049 60.49%
Fish aquatic toxicity + 0.9926 99.26%

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
CHEMBL1951 P21397 Monoamine oxidase A 98.59% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.22% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.49% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.79% 95.56%
CHEMBL2535 P11166 Glucose transporter 91.18% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.09% 86.33%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 89.94% 96.67%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.29% 94.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 89.20% 92.94%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 87.01% 93.03%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.95% 89.00%
CHEMBL1907 P15144 Aminopeptidase N 85.81% 93.31%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 85.78% 80.78%
CHEMBL1255126 O15151 Protein Mdm4 85.57% 90.20%
CHEMBL4208 P20618 Proteasome component C5 85.22% 90.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 85.13% 89.62%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 83.67% 92.38%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.53% 96.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.83% 90.71%
CHEMBL1937 Q92769 Histone deacetylase 2 82.08% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.18% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.76% 99.17%

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.
Dioscorea membranacea

Cross-Links

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PubChem 10869816
LOTUS LTS0145905
wikiData Q82265274