2,4,5,7-Tetrathiaoctane 4,4-dioxide

Details

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Internal ID f3e75aee-580a-4b63-9735-a3d458e7385a
Taxonomy Organosulfur compounds > Sulfonyls
IUPAC Name methylsulfanyl(methylsulfanylmethylsulfonylsulfanyl)methane
SMILES (Canonical) CSCSS(=O)(=O)CSC
SMILES (Isomeric) CSCSS(=O)(=O)CSC
InChI InChI=1S/C4H10O2S4/c1-7-3-9-10(5,6)4-8-2/h3-4H2,1-2H3
InChI Key ZEOQFQWTAWCRFR-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C4H10O2S4
Molecular Weight 218.40 g/mol
Exact Mass 217.95636425 g/mol
Topological Polar Surface Area (TPSA) 118.00 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.69
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 2,4,5,7-Tetrathiaoctane 4,4-dioxide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9403 94.03%
Caco-2 + 0.6766 67.66%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.4198 41.98%
OATP2B1 inhibitior - 0.8500 85.00%
OATP1B1 inhibitior + 0.9660 96.60%
OATP1B3 inhibitior + 0.9443 94.43%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9585 95.85%
P-glycoprotein inhibitior - 0.9569 95.69%
P-glycoprotein substrate - 0.9485 94.85%
CYP3A4 substrate - 0.6789 67.89%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8411 84.11%
CYP3A4 inhibition - 0.9476 94.76%
CYP2C9 inhibition - 0.7409 74.09%
CYP2C19 inhibition - 0.6348 63.48%
CYP2D6 inhibition - 0.8985 89.85%
CYP1A2 inhibition - 0.7497 74.97%
CYP2C8 inhibition - 0.9668 96.68%
CYP inhibitory promiscuity - 0.8647 86.47%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6596 65.96%
Carcinogenicity (trinary) Non-required 0.6521 65.21%
Eye corrosion + 0.5000 50.00%
Eye irritation + 0.9390 93.90%
Skin irritation - 0.6323 63.23%
Skin corrosion - 0.5000 50.00%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6109 61.09%
Micronuclear + 0.7100 71.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation - 0.6127 61.27%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.7934 79.34%
Acute Oral Toxicity (c) III 0.4070 40.70%
Estrogen receptor binding - 0.8530 85.30%
Androgen receptor binding - 0.9133 91.33%
Thyroid receptor binding - 0.7432 74.32%
Glucocorticoid receptor binding - 0.9191 91.91%
Aromatase binding - 0.7989 79.89%
PPAR gamma - 0.8502 85.02%
Honey bee toxicity - 0.7583 75.83%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.7398 73.98%

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
CHEMBL2581 P07339 Cathepsin D 87.44% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 83.53% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.35% 95.56%
CHEMBL226 P30542 Adenosine A1 receptor 81.21% 95.93%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.18% 96.09%

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.
Dioncophyllum thollonii

Cross-Links

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PubChem 10082131
LOTUS LTS0178857
wikiData Q105373469