3-Ethyl-5-hydroxy-2,6,7-trimethoxynaphthalene-1,4-dione

Details

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Internal ID 54a9501d-2515-43d2-996a-d5ff8333d7a3
Taxonomy Benzenoids > Naphthalenes > Naphthoquinones
IUPAC Name 3-ethyl-5-hydroxy-2,6,7-trimethoxynaphthalene-1,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H16O6/c1-5-7-11(16)10-8(12(17)14(7)20-3)6-9(19-2)15(21-4)13(10)18/h6,18H,5H2,1-4H3
InChI Key UAGRZTOQRLUIEG-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H16O6
Molecular Weight 292.28 g/mol
Exact Mass 292.09468823 g/mol
Topological Polar Surface Area (TPSA) 82.10 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.10
H-Bond Acceptor 6
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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3-ETHYL-5-HYDROXY-2,6,7-TRIMETHOXYNAPHTHALENE-1,4-DIONE
3-Ethyl-5-hydroxy-2,6,7-trimethoxy-1,4-naphthalenedione

2D Structure

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2D Structure of 3-Ethyl-5-hydroxy-2,6,7-trimethoxynaphthalene-1,4-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.7146 71.46%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.7775 77.75%
OATP2B1 inhibitior - 0.8590 85.90%
OATP1B1 inhibitior + 0.8876 88.76%
OATP1B3 inhibitior + 0.9445 94.45%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.7325 73.25%
P-glycoprotein inhibitior - 0.8815 88.15%
P-glycoprotein substrate - 0.8827 88.27%
CYP3A4 substrate + 0.5124 51.24%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7987 79.87%
CYP3A4 inhibition - 0.7985 79.85%
CYP2C9 inhibition + 0.5000 50.00%
CYP2C19 inhibition + 0.5697 56.97%
CYP2D6 inhibition - 0.8363 83.63%
CYP1A2 inhibition + 0.7454 74.54%
CYP2C8 inhibition + 0.5171 51.71%
CYP inhibitory promiscuity + 0.7781 77.81%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9324 93.24%
Carcinogenicity (trinary) Non-required 0.5645 56.45%
Eye corrosion - 0.9862 98.62%
Eye irritation + 0.8995 89.95%
Skin irritation - 0.7237 72.37%
Skin corrosion - 0.9660 96.60%
Ames mutagenesis - 0.6237 62.37%
Human Ether-a-go-go-Related Gene inhibition - 0.7119 71.19%
Micronuclear + 0.6218 62.18%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.6293 62.93%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.6258 62.58%
Acute Oral Toxicity (c) III 0.4247 42.47%
Estrogen receptor binding + 0.8176 81.76%
Androgen receptor binding - 0.5170 51.70%
Thyroid receptor binding - 0.6537 65.37%
Glucocorticoid receptor binding + 0.6315 63.15%
Aromatase binding + 0.5971 59.71%
PPAR gamma + 0.6074 60.74%
Honey bee toxicity - 0.9272 92.72%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.9898 98.98%

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
CHEMBL2581 P07339 Cathepsin D 95.37% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.15% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.93% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.65% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.74% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.62% 94.00%
CHEMBL2535 P11166 Glucose transporter 89.36% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.10% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.31% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.31% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 80.95% 94.73%

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.
Lomandra hastilis

Cross-Links

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PubChem 11119876
LOTUS LTS0021463
wikiData Q105268750