6-Ethyl-2,5,7,8-tetrahydroxy-3-methoxynaphthalene-1,4-dione

Details

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Internal ID f1719622-558f-42c3-a574-25735bbee7a5
Taxonomy Benzenoids > Naphthalenes > Naphthoquinones
IUPAC Name 6-ethyl-2,5,7,8-tetrahydroxy-3-methoxynaphthalene-1,4-dione
SMILES (Canonical) CCC1=C(C2=C(C(=C1O)O)C(=O)C(=C(C2=O)OC)O)O
SMILES (Isomeric) CCC1=C(C2=C(C(=C1O)O)C(=O)C(=C(C2=O)OC)O)O
InChI InChI=1S/C13H12O7/c1-3-4-7(14)5-6(9(16)8(4)15)10(17)12(19)13(20-2)11(5)18/h14-16,19H,3H2,1-2H3
InChI Key YBTUDFWVCSHOBG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H12O7
Molecular Weight 280.23 g/mol
Exact Mass 280.05830272 g/mol
Topological Polar Surface Area (TPSA) 124.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 1.16
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-Ethyl-2,5,7,8-tetrahydroxy-3-methoxynaphthalene-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 + 0.9653 96.53%
Caco-2 - 0.5860 58.60%
Blood Brain Barrier - 0.6101 61.01%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6627 66.27%
OATP2B1 inhibitior - 0.8531 85.31%
OATP1B1 inhibitior + 0.8495 84.95%
OATP1B3 inhibitior + 0.9739 97.39%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.8588 85.88%
BSEP inhibitior - 0.9203 92.03%
P-glycoprotein inhibitior - 0.8496 84.96%
P-glycoprotein substrate - 0.9383 93.83%
CYP3A4 substrate - 0.5703 57.03%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8499 84.99%
CYP3A4 inhibition - 0.7155 71.55%
CYP2C9 inhibition - 0.5184 51.84%
CYP2C19 inhibition - 0.6793 67.93%
CYP2D6 inhibition - 0.7131 71.31%
CYP1A2 inhibition + 0.7798 77.98%
CYP2C8 inhibition - 0.8624 86.24%
CYP inhibitory promiscuity + 0.6543 65.43%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9218 92.18%
Carcinogenicity (trinary) Non-required 0.6241 62.41%
Eye corrosion - 0.9841 98.41%
Eye irritation + 0.8655 86.55%
Skin irritation - 0.6640 66.40%
Skin corrosion - 0.8839 88.39%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5623 56.23%
Micronuclear + 0.6859 68.59%
Hepatotoxicity - 0.5467 54.67%
skin sensitisation - 0.6787 67.87%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.5324 53.24%
Acute Oral Toxicity (c) III 0.4443 44.43%
Estrogen receptor binding + 0.8321 83.21%
Androgen receptor binding - 0.6254 62.54%
Thyroid receptor binding - 0.7206 72.06%
Glucocorticoid receptor binding + 0.8368 83.68%
Aromatase binding + 0.5236 52.36%
PPAR gamma - 0.5362 53.62%
Honey bee toxicity - 0.9162 91.62%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9891 98.91%

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 94.23% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.77% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.27% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.41% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.57% 94.45%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 83.98% 92.68%
CHEMBL3401 O75469 Pregnane X receptor 83.30% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.46% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.53% 99.23%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.35% 96.95%

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 136858061
LOTUS LTS0234185
wikiData Q105346050