3-Ethyl-1-methoxyindole

Details

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Internal ID febff3af-17ec-475a-98b6-56043d29b385
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles > 3-alkylindoles
IUPAC Name 3-ethyl-1-methoxyindole
SMILES (Canonical) CCC1=CN(C2=CC=CC=C21)OC
SMILES (Isomeric) CCC1=CN(C2=CC=CC=C21)OC
InChI InChI=1S/C11H13NO/c1-3-9-8-12(13-2)11-7-5-4-6-10(9)11/h4-8H,3H2,1-2H3
InChI Key HBCGVLQXOOVNBP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H13NO
Molecular Weight 175.23 g/mol
Exact Mass 175.099714038 g/mol
Topological Polar Surface Area (TPSA) 14.20 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.26
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Ethyl-1-methoxyindole

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9964 99.64%
Caco-2 + 0.9519 95.19%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.7571 75.71%
Subcellular localzation Mitochondria 0.4584 45.84%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9500 95.00%
OATP1B3 inhibitior + 0.9447 94.47%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8995 89.95%
P-glycoprotein inhibitior - 0.9768 97.68%
P-glycoprotein substrate - 0.9224 92.24%
CYP3A4 substrate - 0.5863 58.63%
CYP2C9 substrate - 0.8151 81.51%
CYP2D6 substrate + 0.3500 35.00%
CYP3A4 inhibition - 0.9528 95.28%
CYP2C9 inhibition - 0.7115 71.15%
CYP2C19 inhibition - 0.6532 65.32%
CYP2D6 inhibition - 0.8343 83.43%
CYP1A2 inhibition + 0.8056 80.56%
CYP2C8 inhibition - 0.8070 80.70%
CYP inhibitory promiscuity - 0.5323 53.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7848 78.48%
Carcinogenicity (trinary) Non-required 0.4271 42.71%
Eye corrosion - 0.9606 96.06%
Eye irritation + 0.9362 93.62%
Skin irritation - 0.7472 74.72%
Skin corrosion - 0.9292 92.92%
Ames mutagenesis + 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5161 51.61%
Micronuclear + 0.6774 67.74%
Hepatotoxicity + 0.6409 64.09%
skin sensitisation - 0.7899 78.99%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.6073 60.73%
Nephrotoxicity - 0.5576 55.76%
Acute Oral Toxicity (c) III 0.6269 62.69%
Estrogen receptor binding - 0.8368 83.68%
Androgen receptor binding - 0.6927 69.27%
Thyroid receptor binding - 0.7892 78.92%
Glucocorticoid receptor binding - 0.9148 91.48%
Aromatase binding - 0.7586 75.86%
PPAR gamma - 0.8715 87.15%
Honey bee toxicity - 0.8649 86.49%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.7220 72.20%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.41% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.31% 95.56%
CHEMBL240 Q12809 HERG 94.16% 89.76%
CHEMBL2581 P07339 Cathepsin D 93.55% 98.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.44% 93.99%
CHEMBL3401 O75469 Pregnane X receptor 85.25% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.23% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.87% 96.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.47% 97.25%

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.
Arabidopsis thaliana
Eutrema halophilum

Cross-Links

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PubChem 68023567
LOTUS LTS0265984
wikiData Q105025209