Methylsulfanyl(methylsulfanylsulfonyl)methane

Details

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Internal ID 9a234479-f706-4e6a-ab41-809436747fc6
Taxonomy Organosulfur compounds > Sulfonyls
IUPAC Name methylsulfanyl(methylsulfanylsulfonyl)methane
SMILES (Canonical) CSCS(=O)(=O)SC
SMILES (Isomeric) CSCS(=O)(=O)SC
InChI InChI=1S/C3H8O2S3/c1-6-3-8(4,5)7-2/h3H2,1-2H3
InChI Key KBKQSWQEBOBFKC-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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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

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There are no found synonyms.

2D Structure

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2D Structure of Methylsulfanyl(methylsulfanylsulfonyl)methane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9599 95.99%
Caco-2 + 0.5140 51.40%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.4368 43.68%
OATP2B1 inhibitior - 0.8675 86.75%
OATP1B1 inhibitior + 0.9599 95.99%
OATP1B3 inhibitior + 0.9436 94.36%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9533 95.33%
P-glycoprotein inhibitior - 0.9816 98.16%
P-glycoprotein substrate - 0.9646 96.46%
CYP3A4 substrate - 0.6993 69.93%
CYP2C9 substrate - 0.8191 81.91%
CYP2D6 substrate - 0.8175 81.75%
CYP3A4 inhibition - 0.9727 97.27%
CYP2C9 inhibition - 0.7556 75.56%
CYP2C19 inhibition - 0.6614 66.14%
CYP2D6 inhibition - 0.9044 90.44%
CYP1A2 inhibition - 0.7155 71.55%
CYP2C8 inhibition - 0.9746 97.46%
CYP inhibitory promiscuity - 0.9243 92.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6696 66.96%
Carcinogenicity (trinary) Non-required 0.6877 68.77%
Eye corrosion + 0.6366 63.66%
Eye irritation + 0.9171 91.71%
Skin irritation - 0.5765 57.65%
Skin corrosion + 0.5447 54.47%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7008 70.08%
Micronuclear + 0.7000 70.00%
Hepatotoxicity + 0.5504 55.04%
skin sensitisation - 0.5910 59.10%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.8353 83.53%
Acute Oral Toxicity (c) III 0.4756 47.56%
Estrogen receptor binding - 0.9048 90.48%
Androgen receptor binding - 0.9314 93.14%
Thyroid receptor binding - 0.8008 80.08%
Glucocorticoid receptor binding - 0.9248 92.48%
Aromatase binding - 0.8653 86.53%
PPAR gamma - 0.9050 90.50%
Honey bee toxicity - 0.6847 68.47%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.7374 73.74%

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
CHEMBL3401 O75469 Pregnane X receptor 86.26% 94.73%
CHEMBL226 P30542 Adenosine A1 receptor 84.60% 95.93%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.94% 96.09%
CHEMBL255 P29275 Adenosine A2b receptor 80.64% 98.59%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.32% 95.56%

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.
Scorodophloeus zenkeri

Cross-Links

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PubChem 86208847
LOTUS LTS0162362
wikiData Q105138313