3-(1H-pyrrol-3-yl)prop-2-enamide

Details

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Internal ID 336c2d1e-e438-4a1a-96bb-69d55473ecff
Taxonomy Organoheterocyclic compounds > Pyrroles > Substituted pyrroles
IUPAC Name 3-(1H-pyrrol-3-yl)prop-2-enamide
SMILES (Canonical) C1=CNC=C1C=CC(=O)N
SMILES (Isomeric) C1=CNC=C1C=CC(=O)N
InChI InChI=1S/C7H8N2O/c8-7(10)2-1-6-3-4-9-5-6/h1-5,9H,(H2,8,10)
InChI Key IXHMPUDATSJPHY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C7H8N2O
Molecular Weight 136.15 g/mol
Exact Mass 136.063662883 g/mol
Topological Polar Surface Area (TPSA) 58.90 Ų
XlogP 0.00
Atomic LogP (AlogP) 0.51
H-Bond Acceptor 1
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(1H-pyrrol-3-yl)prop-2-enamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9963 99.63%
Caco-2 + 0.9514 95.14%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Nucleus 0.2872 28.72%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9767 97.67%
OATP1B3 inhibitior + 0.9528 95.28%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.8244 82.44%
P-glycoprotein inhibitior - 0.9908 99.08%
P-glycoprotein substrate - 0.9444 94.44%
CYP3A4 substrate - 0.7148 71.48%
CYP2C9 substrate - 0.6044 60.44%
CYP2D6 substrate - 0.8619 86.19%
CYP3A4 inhibition - 0.8939 89.39%
CYP2C9 inhibition - 0.7422 74.22%
CYP2C19 inhibition - 0.9195 91.95%
CYP2D6 inhibition - 0.8892 88.92%
CYP1A2 inhibition - 0.7130 71.30%
CYP2C8 inhibition - 0.9371 93.71%
CYP inhibitory promiscuity - 0.7979 79.79%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7300 73.00%
Carcinogenicity (trinary) Warning 0.3719 37.19%
Eye corrosion - 0.6559 65.59%
Eye irritation + 0.9898 98.98%
Skin irritation - 0.6794 67.94%
Skin corrosion - 0.9377 93.77%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7938 79.38%
Micronuclear + 0.6600 66.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.9092 90.92%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.7488 74.88%
Acute Oral Toxicity (c) III 0.6192 61.92%
Estrogen receptor binding - 0.6858 68.58%
Androgen receptor binding - 0.7873 78.73%
Thyroid receptor binding - 0.7915 79.15%
Glucocorticoid receptor binding - 0.7309 73.09%
Aromatase binding + 0.5281 52.81%
PPAR gamma - 0.8479 84.79%
Honey bee toxicity - 0.9742 97.42%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity - 0.8907 89.07%

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 91.34% 96.09%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 86.60% 83.10%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.41% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.76% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.66% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.39% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.95% 96.00%

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 72988089
LOTUS LTS0063022
wikiData Q105122171