(2S)-3-(5-ethylsulfanyl-1,3-dimethylimidazol-1-ium-4-yl)-2-hydroxypropanoate

Details

Top
Internal ID 3ee63013-3cac-4b15-aa2d-fe26f4344cc2
Taxonomy Organosulfur compounds > Thioethers > Aryl thioethers
IUPAC Name (2S)-3-(5-ethylsulfanyl-1,3-dimethylimidazol-1-ium-4-yl)-2-hydroxypropanoate
SMILES (Canonical) CCSC1=C(N(C=[N+]1C)C)CC(C(=O)[O-])O
SMILES (Isomeric) CCSC1=C(N(C=[N+]1C)C)C[C@@H](C(=O)[O-])O
InChI InChI=1S/C10H16N2O3S/c1-4-16-9-7(5-8(13)10(14)15)11(2)6-12(9)3/h6,8,13H,4-5H2,1-3H3/t8-/m0/s1
InChI Key BXLXJEGLLKOWCH-QMMMGPOBSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H16N2O3S
Molecular Weight 244.31 g/mol
Exact Mass 244.08816355 g/mol
Topological Polar Surface Area (TPSA) 94.50 Ų
XlogP 1.20
Atomic LogP (AlogP) -1.39
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (2S)-3-(5-ethylsulfanyl-1,3-dimethylimidazol-1-ium-4-yl)-2-hydroxypropanoate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7960 79.60%
Caco-2 - 0.6798 67.98%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.4637 46.37%
OATP2B1 inhibitior - 0.8486 84.86%
OATP1B1 inhibitior + 0.9144 91.44%
OATP1B3 inhibitior + 0.9369 93.69%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9599 95.99%
P-glycoprotein inhibitior - 0.9465 94.65%
P-glycoprotein substrate - 0.7479 74.79%
CYP3A4 substrate - 0.5360 53.60%
CYP2C9 substrate - 0.7935 79.35%
CYP2D6 substrate - 0.8652 86.52%
CYP3A4 inhibition - 0.9481 94.81%
CYP2C9 inhibition - 0.8485 84.85%
CYP2C19 inhibition - 0.7989 79.89%
CYP2D6 inhibition - 0.9018 90.18%
CYP1A2 inhibition - 0.7725 77.25%
CYP2C8 inhibition - 0.9622 96.22%
CYP inhibitory promiscuity - 0.9082 90.82%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.5210 52.10%
Eye corrosion - 0.9810 98.10%
Eye irritation - 0.8689 86.89%
Skin irritation - 0.7478 74.78%
Skin corrosion - 0.9151 91.51%
Ames mutagenesis - 0.6254 62.54%
Human Ether-a-go-go-Related Gene inhibition - 0.7252 72.52%
Micronuclear + 0.6100 61.00%
Hepatotoxicity + 0.5360 53.60%
skin sensitisation - 0.8453 84.53%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.7716 77.16%
Acute Oral Toxicity (c) III 0.5146 51.46%
Estrogen receptor binding - 0.5410 54.10%
Androgen receptor binding - 0.5214 52.14%
Thyroid receptor binding + 0.5770 57.70%
Glucocorticoid receptor binding - 0.5653 56.53%
Aromatase binding - 0.7772 77.72%
PPAR gamma + 0.6106 61.06%
Honey bee toxicity - 0.9285 92.85%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity - 0.4302 43.02%

Targets

Top

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 97.36% 96.09%
CHEMBL2581 P07339 Cathepsin D 96.62% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.37% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.70% 86.33%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 80.21% 100.00%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 102105743
LOTUS LTS0021865
wikiData Q104948060