4-(1h-Indol-5-yl)but-3-en-2-one

Details

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Internal ID 8aee0471-6441-4939-8d0f-0d3d41488d37
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indoles
IUPAC Name (E)-4-(1H-indol-5-yl)but-3-en-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H11NO/c1-9(14)2-3-10-4-5-12-11(8-10)6-7-13-12/h2-8,13H,1H3/b3-2+
InChI Key GZFUNESZCZCIFV-NSCUHMNNSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H11NO
Molecular Weight 185.22 g/mol
Exact Mass 185.084063974 g/mol
Topological Polar Surface Area (TPSA) 32.90 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.77
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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SCHEMBL4590213
1021910-47-3
EN300-1847956

2D Structure

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2D Structure of 4-(1h-Indol-5-yl)but-3-en-2-one

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 + 0.6473 64.73%
Blood Brain Barrier + 0.8629 86.29%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.3643 36.43%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9469 94.69%
OATP1B3 inhibitior + 0.9669 96.69%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.6412 64.12%
P-glycoprotein inhibitior - 0.9782 97.82%
P-glycoprotein substrate - 0.9101 91.01%
CYP3A4 substrate - 0.6495 64.95%
CYP2C9 substrate - 0.5976 59.76%
CYP2D6 substrate - 0.8328 83.28%
CYP3A4 inhibition - 0.8785 87.85%
CYP2C9 inhibition + 0.5281 52.81%
CYP2C19 inhibition + 0.7964 79.64%
CYP2D6 inhibition - 0.8001 80.01%
CYP1A2 inhibition + 0.8952 89.52%
CYP2C8 inhibition - 0.7283 72.83%
CYP inhibitory promiscuity + 0.5901 59.01%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7800 78.00%
Carcinogenicity (trinary) Non-required 0.5579 55.79%
Eye corrosion - 0.9227 92.27%
Eye irritation + 0.9176 91.76%
Skin irritation + 0.6007 60.07%
Skin corrosion - 0.9522 95.22%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3902 39.02%
Micronuclear + 0.7759 77.59%
Hepatotoxicity - 0.6226 62.26%
skin sensitisation - 0.6837 68.37%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.6947 69.47%
Acute Oral Toxicity (c) III 0.8682 86.82%
Estrogen receptor binding + 0.7412 74.12%
Androgen receptor binding - 0.6106 61.06%
Thyroid receptor binding - 0.6562 65.62%
Glucocorticoid receptor binding - 0.5179 51.79%
Aromatase binding + 0.7077 70.77%
PPAR gamma - 0.7171 71.71%
Honey bee toxicity - 0.9511 95.11%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity - 0.4765 47.65%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.67% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.05% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.25% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.53% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.93% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.27% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.98% 89.00%
CHEMBL2581 P07339 Cathepsin D 85.01% 98.95%
CHEMBL4208 P20618 Proteasome component C5 81.89% 90.00%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 80.67% 91.71%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 80.48% 83.10%

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.
Monodora myristica

Cross-Links

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PubChem 69105643
LOTUS LTS0097506
wikiData Q105024370