1-Ethyl-2-methylnaphthalene

Details

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Internal ID c4425a46-a256-4b24-bf24-5759924b8abb
Taxonomy Benzenoids > Naphthalenes
IUPAC Name 1-ethyl-2-methylnaphthalene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H14/c1-3-12-10(2)8-9-11-6-4-5-7-13(11)12/h4-9H,3H2,1-2H3
InChI Key INUWBHWKAMVTNU-UHFFFAOYSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C13H14
Molecular Weight 170.25 g/mol
Exact Mass 170.109550447 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 4.70
Atomic LogP (AlogP) 3.71
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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methylethylnaphthalene
DTXSID001346306
17057-93-1

2D Structure

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2D Structure of 1-Ethyl-2-methylnaphthalene

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 + 0.9125 91.25%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Lysosomes 0.6825 68.25%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8968 89.68%
OATP1B3 inhibitior + 0.9574 95.74%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.5770 57.70%
P-glycoprotein inhibitior - 0.9844 98.44%
P-glycoprotein substrate - 0.9493 94.93%
CYP3A4 substrate - 0.6698 66.98%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4300 43.00%
CYP3A4 inhibition - 0.8791 87.91%
CYP2C9 inhibition - 0.7365 73.65%
CYP2C19 inhibition + 0.5662 56.62%
CYP2D6 inhibition - 0.8344 83.44%
CYP1A2 inhibition + 0.7385 73.85%
CYP2C8 inhibition - 0.8105 81.05%
CYP inhibitory promiscuity + 0.7994 79.94%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Non-required 0.4877 48.77%
Eye corrosion - 0.8647 86.47%
Eye irritation + 0.9446 94.46%
Skin irritation + 0.6754 67.54%
Skin corrosion - 0.9671 96.71%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4645 46.45%
Micronuclear - 0.9008 90.08%
Hepatotoxicity + 0.6476 64.76%
skin sensitisation + 0.8958 89.58%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.8222 82.22%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.7817 78.17%
Acute Oral Toxicity (c) II 0.5360 53.60%
Estrogen receptor binding - 0.7505 75.05%
Androgen receptor binding + 0.5806 58.06%
Thyroid receptor binding - 0.7332 73.32%
Glucocorticoid receptor binding - 0.8675 86.75%
Aromatase binding - 0.6412 64.12%
PPAR gamma - 0.7110 71.10%
Honey bee toxicity - 0.9746 97.46%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity + 0.9973 99.73%

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
CHEMBL240 Q12809 HERG 93.99% 89.76%
CHEMBL2885 P07451 Carbonic anhydrase III 90.24% 87.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.22% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 88.89% 94.73%
CHEMBL2581 P07339 Cathepsin D 86.34% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 85.76% 89.63%
CHEMBL3959 P16083 Quinone reductase 2 82.13% 89.49%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.36% 96.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.32% 93.65%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.13% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.17% 86.33%
CHEMBL1936 P10721 Stem cell growth factor receptor 80.09% 84.17%

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.
Gossypium hirsutum

Cross-Links

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PubChem 15645217
LOTUS LTS0087306
wikiData Q81986082