3-(4-Methoxyphenyl)-1-(pyrrol-1-yl)propan-1-one

Details

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Internal ID 2092c274-6710-4d05-901f-bfe93fc50225
Taxonomy Benzenoids > Phenol ethers > Anisoles
IUPAC Name 3-(4-methoxyphenyl)-1-pyrrol-1-ylpropan-1-one
SMILES (Canonical) COC1=CC=C(C=C1)CCC(=O)N2C=CC=C2
SMILES (Isomeric) COC1=CC=C(C=C1)CCC(=O)N2C=CC=C2
InChI InChI=1S/C14H15NO2/c1-17-13-7-4-12(5-8-13)6-9-14(16)15-10-2-3-11-15/h2-5,7-8,10-11H,6,9H2,1H3
InChI Key DLHIPWLSQXISAB-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H15NO2
Molecular Weight 229.27 g/mol
Exact Mass 229.110278721 g/mol
Topological Polar Surface Area (TPSA) 31.20 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.77
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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448905-82-6
AKOS025288606
3-(4-methoxyphenyl)-1-pyrrol-1-ylpropan-1-one
1-(1H-Pyrrole-1-yl)-3-(4-methoxyphenyl)-1-propanone

2D Structure

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2D Structure of 3-(4-Methoxyphenyl)-1-(pyrrol-1-yl)propan-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.9535 95.35%
Blood Brain Barrier + 0.8817 88.17%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7645 76.45%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9124 91.24%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7348 73.48%
BSEP inhibitior - 0.5789 57.89%
P-glycoprotein inhibitior - 0.9702 97.02%
P-glycoprotein substrate - 0.9097 90.97%
CYP3A4 substrate - 0.5315 53.15%
CYP2C9 substrate + 0.8032 80.32%
CYP2D6 substrate - 0.8122 81.22%
CYP3A4 inhibition - 0.7633 76.33%
CYP2C9 inhibition + 0.7044 70.44%
CYP2C19 inhibition + 0.7923 79.23%
CYP2D6 inhibition - 0.9172 91.72%
CYP1A2 inhibition + 0.7358 73.58%
CYP2C8 inhibition - 0.7015 70.15%
CYP inhibitory promiscuity + 0.7332 73.32%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.4877 48.77%
Eye corrosion - 0.9746 97.46%
Eye irritation - 0.6039 60.39%
Skin irritation - 0.7680 76.80%
Skin corrosion - 0.9150 91.50%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6631 66.31%
Micronuclear + 0.5800 58.00%
Hepatotoxicity - 0.6465 64.65%
skin sensitisation - 0.9187 91.87%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.6537 65.37%
Nephrotoxicity - 0.7392 73.92%
Acute Oral Toxicity (c) III 0.7198 71.98%
Estrogen receptor binding + 0.5871 58.71%
Androgen receptor binding + 0.6785 67.85%
Thyroid receptor binding - 0.6717 67.17%
Glucocorticoid receptor binding - 0.6154 61.54%
Aromatase binding - 0.5235 52.35%
PPAR gamma - 0.7356 73.56%
Honey bee toxicity - 0.9368 93.68%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity - 0.9262 92.62%

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 98.51% 96.09%
CHEMBL2581 P07339 Cathepsin D 96.48% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.11% 86.33%
CHEMBL4208 P20618 Proteasome component C5 90.51% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.65% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.85% 95.56%
CHEMBL3437 Q16853 Amine oxidase, copper containing 85.07% 94.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.44% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.34% 85.14%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.84% 95.50%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 83.07% 86.92%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.01% 96.95%
CHEMBL3492 P49721 Proteasome Macropain subunit 80.88% 90.24%

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.
Acanthosyris paulo-alvinii
Aglaia perviridis
Ardisia japonica
Betula alnoides
Phoebe grandis
Piper sarmentosum
Rubus pileatus

Cross-Links

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PubChem 51136593
NPASS NPC299744