5-Hydroxy-3-(2-hydroxyethyl)-2-methylnaphthalene-1,4-dione

Details

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Internal ID 10acf83e-5f5b-4fae-a460-7387bd3829ba
Taxonomy Benzenoids > Naphthalenes > Naphthoquinones
IUPAC Name 5-hydroxy-3-(2-hydroxyethyl)-2-methylnaphthalene-1,4-dione
SMILES (Canonical) CC1=C(C(=O)C2=C(C1=O)C=CC=C2O)CCO
SMILES (Isomeric) CC1=C(C(=O)C2=C(C1=O)C=CC=C2O)CCO
InChI InChI=1S/C13H12O4/c1-7-8(5-6-14)13(17)11-9(12(7)16)3-2-4-10(11)15/h2-4,14-15H,5-6H2,1H3
InChI Key AJFLZDTWEGZZRX-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C13H12O4
Molecular Weight 232.23 g/mol
Exact Mass 232.07355886 g/mol
Topological Polar Surface Area (TPSA) 74.60 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.47
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Hydroxy-3-(2-hydroxyethyl)-2-methylnaphthalene-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 + 0.9965 99.65%
Caco-2 - 0.5335 53.35%
Blood Brain Barrier - 0.6072 60.72%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.8251 82.51%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8999 89.99%
OATP1B3 inhibitior + 0.9512 95.12%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.7608 76.08%
BSEP inhibitior - 0.8553 85.53%
P-glycoprotein inhibitior - 0.9845 98.45%
P-glycoprotein substrate - 0.8858 88.58%
CYP3A4 substrate - 0.5232 52.32%
CYP2C9 substrate - 0.8063 80.63%
CYP2D6 substrate - 0.8338 83.38%
CYP3A4 inhibition - 0.5479 54.79%
CYP2C9 inhibition + 0.5478 54.78%
CYP2C19 inhibition - 0.5196 51.96%
CYP2D6 inhibition - 0.6638 66.38%
CYP1A2 inhibition + 0.8561 85.61%
CYP2C8 inhibition - 0.8535 85.35%
CYP inhibitory promiscuity + 0.5437 54.37%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8228 82.28%
Carcinogenicity (trinary) Non-required 0.6903 69.03%
Eye corrosion - 0.9919 99.19%
Eye irritation + 0.8713 87.13%
Skin irritation - 0.6402 64.02%
Skin corrosion - 0.9399 93.99%
Ames mutagenesis + 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7976 79.76%
Micronuclear - 0.7300 73.00%
Hepatotoxicity + 0.6336 63.36%
skin sensitisation - 0.5905 59.05%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity + 0.7637 76.37%
Acute Oral Toxicity (c) III 0.6920 69.20%
Estrogen receptor binding - 0.5897 58.97%
Androgen receptor binding + 0.5289 52.89%
Thyroid receptor binding - 0.7774 77.74%
Glucocorticoid receptor binding + 0.5542 55.42%
Aromatase binding - 0.6908 69.08%
PPAR gamma + 0.5335 53.35%
Honey bee toxicity - 0.9596 95.96%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9579 95.79%

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 98.30% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.19% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 91.67% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.14% 99.23%
CHEMBL1951 P21397 Monoamine oxidase A 86.43% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.19% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.35% 99.15%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.19% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.17% 96.09%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 84.37% 96.37%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.04% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 83.36% 94.75%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.28% 96.67%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.79% 86.92%
CHEMBL2535 P11166 Glucose transporter 81.60% 98.75%
CHEMBL1907 P15144 Aminopeptidase N 80.53% 93.31%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 80.38% 93.03%

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.
Diospyros maritima

Cross-Links

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PubChem 10609591
LOTUS LTS0233572
wikiData Q104913151