S-((methylthio)methyl) methanesulfonothioate

Details

Top
Internal ID a77d6cfc-84f3-4d14-8720-a06b1d4311cc
Taxonomy Organosulfur compounds > Sulfonyls
IUPAC Name methylsulfanyl(methylsulfonylsulfanyl)methane
SMILES (Canonical) CSCSS(=O)(=O)C
SMILES (Isomeric) CSCSS(=O)(=O)C
InChI InChI=1S/C3H8O2S3/c1-6-3-7-8(2,4)5/h3H2,1-2H3
InChI Key SYAVJILWAIKGCS-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C3H8O2S3
Molecular Weight 172.30 g/mol
Exact Mass 171.96864301 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.00
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

Top
SYAVJILWAIKGCS-UHFFFAOYSA-N
Methylthio(methylthio-methyl)sulfone,
S-((methylthio)methyl) methanesulfonothioate
Methanesulfonothioic acid, S-[(methylthio)methyl] ester

2D Structure

Top
2D Structure of S-((methylthio)methyl) methanesulfonothioate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9617 96.17%
Caco-2 + 0.5788 57.88%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Lysosomes 0.4257 42.57%
OATP2B1 inhibitior - 0.8597 85.97%
OATP1B1 inhibitior + 0.9622 96.22%
OATP1B3 inhibitior + 0.9439 94.39%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9462 94.62%
P-glycoprotein inhibitior - 0.9702 97.02%
P-glycoprotein substrate - 0.9692 96.92%
CYP3A4 substrate - 0.7068 70.68%
CYP2C9 substrate - 0.8075 80.75%
CYP2D6 substrate - 0.8364 83.64%
CYP3A4 inhibition - 0.9785 97.85%
CYP2C9 inhibition - 0.7366 73.66%
CYP2C19 inhibition - 0.6565 65.65%
CYP2D6 inhibition - 0.9024 90.24%
CYP1A2 inhibition - 0.6930 69.30%
CYP2C8 inhibition - 0.9793 97.93%
CYP inhibitory promiscuity - 0.9202 92.02%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6596 65.96%
Carcinogenicity (trinary) Non-required 0.6795 67.95%
Eye corrosion + 0.6835 68.35%
Eye irritation + 0.8919 89.19%
Skin irritation - 0.5382 53.82%
Skin corrosion + 0.6177 61.77%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7795 77.95%
Micronuclear + 0.7200 72.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.5486 54.86%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.7383 73.83%
Acute Oral Toxicity (c) III 0.4644 46.44%
Estrogen receptor binding - 0.7859 78.59%
Androgen receptor binding - 0.9316 93.16%
Thyroid receptor binding - 0.7909 79.09%
Glucocorticoid receptor binding - 0.9375 93.75%
Aromatase binding - 0.8626 86.26%
PPAR gamma - 0.8678 86.78%
Honey bee toxicity - 0.7463 74.63%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.8460 84.60%

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
CHEMBL2581 P07339 Cathepsin D 90.07% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.25% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.96% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.27% 96.00%
CHEMBL3401 O75469 Pregnane X receptor 81.09% 94.73%

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.
Scorodophloeus zenkeri

Cross-Links

Top
PubChem 10965006
LOTUS LTS0148621
wikiData Q105263451