N-Ethylpyrrole

Details

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Internal ID 0847019f-6032-45a1-81eb-1c34084e4f0d
Taxonomy Organoheterocyclic compounds > Pyrroles > Substituted pyrroles
IUPAC Name 1-ethylpyrrole
SMILES (Canonical) CCN1C=CC=C1
SMILES (Isomeric) CCN1C=CC=C1
InChI InChI=1S/C6H9N/c1-2-7-5-3-4-6-7/h3-6H,2H2,1H3
InChI Key VPUAYOJTHRDUTK-UHFFFAOYSA-N
Popularity 32 references in papers

Physical and Chemical Properties

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Molecular Formula C6H9N
Molecular Weight 95.14 g/mol
Exact Mass 95.073499291 g/mol
Topological Polar Surface Area (TPSA) 4.90 Ų
XlogP 1.00
Atomic LogP (AlogP) 1.51
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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1-Ethylpyrrole
617-92-5
1-Ethyl-1H-pyrrole
1H-Pyrrole, 1-ethyl-
Pyrrole, 1-ethyl-
ethylpyrrole
N-Ethylpyrrole,
JCK8RWU2W2
NSC-6756
1-ethylpyrrol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of N-Ethylpyrrole

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9772 97.72%
Caco-2 + 0.9266 92.66%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Lysosomes 0.5237 52.37%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9512 95.12%
OATP1B3 inhibitior + 0.9526 95.26%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.9017 90.17%
P-glycoprotein inhibitior - 0.9886 98.86%
P-glycoprotein substrate - 0.9712 97.12%
CYP3A4 substrate - 0.8206 82.06%
CYP2C9 substrate - 0.8209 82.09%
CYP2D6 substrate - 0.7916 79.16%
CYP3A4 inhibition - 0.9707 97.07%
CYP2C9 inhibition - 0.7770 77.70%
CYP2C19 inhibition - 0.6971 69.71%
CYP2D6 inhibition - 0.8137 81.37%
CYP1A2 inhibition - 0.5410 54.10%
CYP2C8 inhibition - 0.9839 98.39%
CYP inhibitory promiscuity + 0.6853 68.53%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Warning 0.5602 56.02%
Eye corrosion + 0.9507 95.07%
Eye irritation + 0.9693 96.93%
Skin irritation + 0.6971 69.71%
Skin corrosion + 0.7082 70.82%
Ames mutagenesis - 0.7970 79.70%
Human Ether-a-go-go-Related Gene inhibition - 0.6576 65.76%
Micronuclear - 0.6500 65.00%
Hepatotoxicity + 0.7625 76.25%
skin sensitisation - 0.7770 77.70%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity - 0.6365 63.65%
Acute Oral Toxicity (c) II 0.5218 52.18%
Estrogen receptor binding - 0.9346 93.46%
Androgen receptor binding - 0.6281 62.81%
Thyroid receptor binding - 0.8470 84.70%
Glucocorticoid receptor binding - 0.8108 81.08%
Aromatase binding - 0.8403 84.03%
PPAR gamma - 0.8812 88.12%
Honey bee toxicity - 0.9576 95.76%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity - 0.7030 70.30%

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 91.09% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.12% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.30% 86.33%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.24% 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.
Coffea arabica
Santalum album

Cross-Links

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PubChem 185226
NPASS NPC268638
LOTUS LTS0017516
wikiData Q105291005