(2R)-2-(5-ethylsulfanyl-1,3-dimethylimidazol-1-ium-4-yl)-2-methoxyacetate

Details

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Internal ID a62bdd6c-6c12-41f8-870e-46e31b0610fe
Taxonomy Organosulfur compounds > Thioethers > Aryl thioethers
IUPAC Name (2R)-2-(5-ethylsulfanyl-1,3-dimethylimidazol-1-ium-4-yl)-2-methoxyacetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16N2O3S/c1-5-16-9-7(8(15-4)10(13)14)11(2)6-12(9)3/h6,8H,5H2,1-4H3/t8-/m1/s1
InChI Key OONRYSCSFGQITJ-MRVPVSSYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16N2O3S
Molecular Weight 244.31 g/mol
Exact Mass 244.08816355 g/mol
Topological Polar Surface Area (TPSA) 83.50 Ų
XlogP 1.50
Atomic LogP (AlogP) -0.60
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R)-2-(5-ethylsulfanyl-1,3-dimethylimidazol-1-ium-4-yl)-2-methoxyacetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6119 61.19%
Caco-2 + 0.5465 54.65%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.5710 57.10%
OATP2B1 inhibitior - 0.8559 85.59%
OATP1B1 inhibitior + 0.8977 89.77%
OATP1B3 inhibitior + 0.9411 94.11%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7598 75.98%
BSEP inhibitior - 0.9481 94.81%
P-glycoprotein inhibitior - 0.9155 91.55%
P-glycoprotein substrate - 0.7832 78.32%
CYP3A4 substrate - 0.5149 51.49%
CYP2C9 substrate - 0.7948 79.48%
CYP2D6 substrate - 0.8935 89.35%
CYP3A4 inhibition - 0.9173 91.73%
CYP2C9 inhibition - 0.6676 66.76%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.9180 91.80%
CYP1A2 inhibition + 0.5720 57.20%
CYP2C8 inhibition - 0.9037 90.37%
CYP inhibitory promiscuity + 0.7123 71.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.4552 45.52%
Eye corrosion - 0.9833 98.33%
Eye irritation - 0.9263 92.63%
Skin irritation - 0.7588 75.88%
Skin corrosion - 0.9251 92.51%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3674 36.74%
Micronuclear + 0.6500 65.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.8578 85.78%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.6293 62.93%
Acute Oral Toxicity (c) III 0.5433 54.33%
Estrogen receptor binding - 0.6689 66.89%
Androgen receptor binding + 0.6400 64.00%
Thyroid receptor binding - 0.5145 51.45%
Glucocorticoid receptor binding - 0.8814 88.14%
Aromatase binding - 0.7796 77.96%
PPAR gamma - 0.4900 49.00%
Honey bee toxicity - 0.8845 88.45%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5855 58.55%
Fish aquatic toxicity - 0.3944 39.44%

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 97.72% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.05% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.84% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.05% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.30% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.95% 94.45%

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 102105745
LOTUS LTS0136265
wikiData Q105195507