4-Hydroxy-4-(4-methoxyphenyl)-1-methyl-5-sulfanylideneimidazolidin-2-one

Details

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Internal ID 1036a8c2-e6dd-47fa-8cac-b08626ad18f9
Taxonomy Organoheterocyclic compounds > Azolidines > Imidazolidines > Phenylimidazolidines
IUPAC Name 4-hydroxy-4-(4-methoxyphenyl)-1-methyl-5-sulfanylideneimidazolidin-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H12N2O3S/c1-13-9(17)11(15,12-10(13)14)7-3-5-8(16-2)6-4-7/h3-6,15H,1-2H3,(H,12,14)
InChI Key PDNVZYVQLWPSRF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H12N2O3S
Molecular Weight 252.29 g/mol
Exact Mass 252.05686342 g/mol
Topological Polar Surface Area (TPSA) 93.90 Ų
XlogP 0.60
Atomic LogP (AlogP) 0.82
H-Bond Acceptor 4
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 4-Hydroxy-4-(4-methoxyphenyl)-1-methyl-5-sulfanylideneimidazolidin-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 + 0.8405 84.05%
Caco-2 + 0.8020 80.20%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.7228 72.28%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9562 95.62%
OATP1B3 inhibitior + 0.9421 94.21%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5436 54.36%
P-glycoprotein inhibitior - 0.9418 94.18%
P-glycoprotein substrate - 0.9332 93.32%
CYP3A4 substrate - 0.5632 56.32%
CYP2C9 substrate - 0.5918 59.18%
CYP2D6 substrate - 0.8077 80.77%
CYP3A4 inhibition - 0.7851 78.51%
CYP2C9 inhibition - 0.5476 54.76%
CYP2C19 inhibition + 0.5079 50.79%
CYP2D6 inhibition - 0.9065 90.65%
CYP1A2 inhibition - 0.5796 57.96%
CYP2C8 inhibition - 0.9677 96.77%
CYP inhibitory promiscuity - 0.7191 71.91%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.6145 61.45%
Eye corrosion - 0.9849 98.49%
Eye irritation - 0.9187 91.87%
Skin irritation - 0.7737 77.37%
Skin corrosion - 0.9313 93.13%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5659 56.59%
Micronuclear + 0.9200 92.00%
Hepatotoxicity + 0.5835 58.35%
skin sensitisation - 0.8627 86.27%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.6710 67.10%
Acute Oral Toxicity (c) III 0.6580 65.80%
Estrogen receptor binding + 0.8449 84.49%
Androgen receptor binding + 0.6706 67.06%
Thyroid receptor binding + 0.7043 70.43%
Glucocorticoid receptor binding + 0.6479 64.79%
Aromatase binding + 0.6978 69.78%
PPAR gamma + 0.5290 52.90%
Honey bee toxicity - 0.9489 94.89%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity - 0.4063 40.63%

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 96.88% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.33% 95.56%
CHEMBL4208 P20618 Proteasome component C5 94.21% 90.00%
CHEMBL2581 P07339 Cathepsin D 93.08% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.76% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.89% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.55% 94.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.50% 93.99%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.21% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.86% 86.33%

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 15287466
LOTUS LTS0089954
wikiData Q105206621