3-ethyl-1H-indole

Details

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Internal ID 974c12c3-b126-48c9-9440-b2647ab87269
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles > 3-alkylindoles
IUPAC Name 3-ethyl-1H-indole
SMILES (Canonical) CCC1=CNC2=CC=CC=C21
SMILES (Isomeric) CCC1=CNC2=CC=CC=C21
InChI InChI=1S/C10H11N/c1-2-8-7-11-10-6-4-3-5-9(8)10/h3-7,11H,2H2,1H3
InChI Key GOVXKUCVZUROAN-UHFFFAOYSA-N
Popularity 39 references in papers

Physical and Chemical Properties

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Molecular Formula C10H11N
Molecular Weight 145.20 g/mol
Exact Mass 145.089149355 g/mol
Topological Polar Surface Area (TPSA) 15.80 Ų
XlogP 3.00
Atomic LogP (AlogP) 2.73
H-Bond Acceptor 0
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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1484-19-1
1H-Indole, 3-ethyl-
3-ethylindole
3-ethyl-indole
NSC289350
SCHEMBL90504
SCHEMBL747112
DTXSID00314851
BAA48419
MFCD01881367
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-ethyl-1H-indole

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 + 0.8492 84.92%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.6944 69.44%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9547 95.47%
OATP1B3 inhibitior + 0.9565 95.65%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8062 80.62%
P-glycoprotein inhibitior - 0.9917 99.17%
P-glycoprotein substrate - 0.9438 94.38%
CYP3A4 substrate - 0.6236 62.36%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate + 0.4146 41.46%
CYP3A4 inhibition - 0.8479 84.79%
CYP2C9 inhibition - 0.6035 60.35%
CYP2C19 inhibition + 0.7184 71.84%
CYP2D6 inhibition + 0.6120 61.20%
CYP1A2 inhibition + 0.8443 84.43%
CYP2C8 inhibition - 0.9286 92.86%
CYP inhibitory promiscuity + 0.6410 64.10%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.5706 57.06%
Eye corrosion - 0.9425 94.25%
Eye irritation + 0.9799 97.99%
Skin irritation + 0.4907 49.07%
Skin corrosion - 0.8830 88.30%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5169 51.69%
Micronuclear + 0.7000 70.00%
Hepatotoxicity - 0.5427 54.27%
skin sensitisation - 0.6528 65.28%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.6812 68.12%
Acute Oral Toxicity (c) III 0.8232 82.32%
Estrogen receptor binding - 0.8537 85.37%
Androgen receptor binding - 0.8440 84.40%
Thyroid receptor binding - 0.8440 84.40%
Glucocorticoid receptor binding - 0.8881 88.81%
Aromatase binding - 0.6933 69.33%
PPAR gamma - 0.7849 78.49%
Honey bee toxicity - 0.9399 93.99%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.7446 74.46%

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 94.52% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.43% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.66% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.64% 96.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.56% 93.99%
CHEMBL3155 P34969 Serotonin 7 (5-HT7) receptor 87.45% 90.71%
CHEMBL255 P29275 Adenosine A2b receptor 86.82% 98.59%
CHEMBL3401 O75469 Pregnane X receptor 83.87% 94.73%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.85% 92.62%
CHEMBL3310 Q96DB2 Histone deacetylase 11 81.34% 88.56%

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.
Eutrema halophilum

Cross-Links

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PubChem 324305
LOTUS LTS0002596
wikiData Q82067286