Ethyl (methylthio)acetate

Details

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Internal ID 3b9f8197-9d77-4c7b-a682-02f7ae93da72
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Carboxylic acid derivatives > Carboxylic acid esters
IUPAC Name ethyl 2-methylsulfanylacetate
SMILES (Canonical) CCOC(=O)CSC
SMILES (Isomeric) CCOC(=O)CSC
InChI InChI=1S/C5H10O2S/c1-3-7-5(6)4-8-2/h3-4H2,1-2H3
InChI Key MDIAKIHKBBNYHF-UHFFFAOYSA-N
Popularity 24 references in papers

Physical and Chemical Properties

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Molecular Formula C5H10O2S
Molecular Weight 134.20 g/mol
Exact Mass 134.04015073 g/mol
Topological Polar Surface Area (TPSA) 51.60 Ų
XlogP 1.20
Atomic LogP (AlogP) 0.91
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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4455-13-4
Ethyl 2-(methylthio)acetate
ethyl 2-methylsulfanylacetate
Acetic acid, (methylthio)-, ethyl ester
Ethyl 2-(methylthio)-acetate
ethyl 2-(methylsulfanyl)acetate
Ethyl alpha-(methylthio)acetate
(Methylthio)acetic acid ethyl ester
methylsulfanyl-acetic acid ethyl ester
Ethyl .alpha.(methylthio)acetate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Ethyl (methylthio)acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9882 98.82%
Caco-2 + 0.6546 65.46%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.5976 59.76%
OATP2B1 inhibitior - 0.8484 84.84%
OATP1B1 inhibitior + 0.9460 94.60%
OATP1B3 inhibitior + 0.9395 93.95%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9028 90.28%
P-glycoprotein inhibitior - 0.9871 98.71%
P-glycoprotein substrate - 0.9931 99.31%
CYP3A4 substrate - 0.6439 64.39%
CYP2C9 substrate - 0.6165 61.65%
CYP2D6 substrate - 0.8830 88.30%
CYP3A4 inhibition - 0.9745 97.45%
CYP2C9 inhibition - 0.9323 93.23%
CYP2C19 inhibition - 0.9194 91.94%
CYP2D6 inhibition - 0.9366 93.66%
CYP1A2 inhibition - 0.7639 76.39%
CYP2C8 inhibition - 0.9417 94.17%
CYP inhibitory promiscuity - 0.8971 89.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5100 51.00%
Carcinogenicity (trinary) Non-required 0.5821 58.21%
Eye corrosion + 0.9429 94.29%
Eye irritation + 0.9899 98.99%
Skin irritation - 0.5995 59.95%
Skin corrosion - 0.9610 96.10%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7547 75.47%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.5130 51.30%
skin sensitisation + 0.6812 68.12%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.7454 74.54%
Acute Oral Toxicity (c) III 0.6443 64.43%
Estrogen receptor binding - 0.9548 95.48%
Androgen receptor binding - 0.9589 95.89%
Thyroid receptor binding - 0.9382 93.82%
Glucocorticoid receptor binding - 0.9404 94.04%
Aromatase binding - 0.8712 87.12%
PPAR gamma - 0.9295 92.95%
Honey bee toxicity - 0.9033 90.33%
Biodegradation + 0.9000 90.00%
Crustacea aquatic toxicity + 0.6345 63.45%
Fish aquatic toxicity + 0.6629 66.29%

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 92.68% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 91.74% 89.63%
CHEMBL4040 P28482 MAP kinase ERK2 87.24% 83.82%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.87% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 85.61% 97.21%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.12% 99.17%

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.
Cucumis melo
Rauvolfia sumatrana

Cross-Links

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PubChem 78199
LOTUS LTS0013406
wikiData Q105310168