2-Hydroxyethyl-3-methyl-1,4-naphthoquinone

Details

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Internal ID 761fd679-e0bd-435d-9521-0d391a0f8099
Taxonomy Benzenoids > Naphthalenes > Naphthoquinones
IUPAC Name 2-(2-hydroxyethyl)-3-methylnaphthalene-1,4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H12O3/c1-8-9(6-7-14)13(16)11-5-3-2-4-10(11)12(8)15/h2-5,14H,6-7H2,1H3
InChI Key XICWGGRIGJUNJP-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C13H12O3
Molecular Weight 216.23 g/mol
Exact Mass 216.078644241 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 0.90
Atomic LogP (AlogP) 1.76
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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CHEMBL3259983
2-(2-hydroxyethyl)-3-methylnaphthalene-1,4-dione

2D Structure

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2D Structure of 2-Hydroxyethyl-3-methyl-1,4-naphthoquinone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.5075 50.75%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.8390 83.90%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9209 92.09%
OATP1B3 inhibitior + 0.9607 96.07%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.8816 88.16%
P-glycoprotein inhibitior - 0.9865 98.65%
P-glycoprotein substrate - 0.9659 96.59%
CYP3A4 substrate - 0.6104 61.04%
CYP2C9 substrate - 0.8006 80.06%
CYP2D6 substrate - 0.8117 81.17%
CYP3A4 inhibition - 0.5742 57.42%
CYP2C9 inhibition + 0.5409 54.09%
CYP2C19 inhibition + 0.6325 63.25%
CYP2D6 inhibition - 0.5548 55.48%
CYP1A2 inhibition + 0.8366 83.66%
CYP2C8 inhibition - 0.9476 94.76%
CYP inhibitory promiscuity - 0.5373 53.73%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8528 85.28%
Carcinogenicity (trinary) Non-required 0.6941 69.41%
Eye corrosion - 0.9912 99.12%
Eye irritation + 0.7774 77.74%
Skin irritation - 0.5847 58.47%
Skin corrosion - 0.9420 94.20%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7170 71.70%
Micronuclear - 0.8151 81.51%
Hepatotoxicity - 0.5316 53.16%
skin sensitisation + 0.5000 50.00%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.6618 66.18%
Acute Oral Toxicity (c) III 0.6582 65.82%
Estrogen receptor binding - 0.6183 61.83%
Androgen receptor binding + 0.5733 57.33%
Thyroid receptor binding - 0.7407 74.07%
Glucocorticoid receptor binding - 0.5893 58.93%
Aromatase binding - 0.6045 60.45%
PPAR gamma - 0.5891 58.91%
Honey bee toxicity - 0.9391 93.91%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9236 92.36%

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 97.73% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.72% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 87.27% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.76% 96.09%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 83.29% 96.67%
CHEMBL1907 P15144 Aminopeptidase N 82.79% 93.31%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.46% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.06% 99.23%

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 10059153
LOTUS LTS0236118
wikiData Q75069406