Methane, (methylsulfonyl)(methylthio)-

Details

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Internal ID 5275a019-8277-4d81-91f5-7d273678de87
Taxonomy Organosulfur compounds > Sulfonyls > Sulfones
IUPAC Name methylsulfanyl(methylsulfonyl)methane
SMILES (Canonical) CSCS(=O)(=O)C
SMILES (Isomeric) CSCS(=O)(=O)C
InChI InChI=1S/C3H8O2S2/c1-6-3-7(2,4)5/h3H2,1-2H3
InChI Key MPHBIACXKTZAFW-UHFFFAOYSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C3H8O2S2
Molecular Weight 140.23 g/mol
Exact Mass 139.99657184 g/mol
Topological Polar Surface Area (TPSA) 67.80 Ų
XlogP 0.30
Atomic LogP (AlogP) 0.35
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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20163-71-7
methylsulfanyl(methylsulfonyl)methane
Methyl((methylsulfonyl)methyl)sulfane
NSC714610
SCHEMBL3151806
2,4-Dithiapentane 2,2-dioxide
DTXSID80328012
MPHBIACXKTZAFW-UHFFFAOYSA-N
methylsulfonyl-methylsulfanyl-methane
Methyl (methylsulfonyl)methyl sulfide
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Methane, (methylsulfonyl)(methylthio)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9322 93.22%
Caco-2 + 0.5743 57.43%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.4685 46.85%
OATP2B1 inhibitior - 0.8655 86.55%
OATP1B1 inhibitior + 0.9535 95.35%
OATP1B3 inhibitior + 0.9455 94.55%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9211 92.11%
P-glycoprotein inhibitior - 0.9738 97.38%
P-glycoprotein substrate - 0.9715 97.15%
CYP3A4 substrate - 0.7349 73.49%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7892 78.92%
CYP3A4 inhibition - 0.9728 97.28%
CYP2C9 inhibition - 0.8030 80.30%
CYP2C19 inhibition - 0.7104 71.04%
CYP2D6 inhibition - 0.9084 90.84%
CYP1A2 inhibition - 0.7672 76.72%
CYP2C8 inhibition - 0.9915 99.15%
CYP inhibitory promiscuity - 0.9284 92.84%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6796 67.96%
Carcinogenicity (trinary) Non-required 0.6684 66.84%
Eye corrosion + 0.8369 83.69%
Eye irritation + 0.9734 97.34%
Skin irritation - 0.6097 60.97%
Skin corrosion + 0.5936 59.36%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7226 72.26%
Micronuclear + 0.6200 62.00%
Hepatotoxicity + 0.6254 62.54%
skin sensitisation - 0.5450 54.50%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.7925 79.25%
Acute Oral Toxicity (c) III 0.5030 50.30%
Estrogen receptor binding - 0.8914 89.14%
Androgen receptor binding - 0.9372 93.72%
Thyroid receptor binding - 0.8351 83.51%
Glucocorticoid receptor binding - 0.9401 94.01%
Aromatase binding - 0.8717 87.17%
PPAR gamma - 0.9141 91.41%
Honey bee toxicity - 0.6954 69.54%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity - 0.6864 68.64%

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
CHEMBL226 P30542 Adenosine A1 receptor 84.60% 95.93%
CHEMBL2581 P07339 Cathepsin D 83.61% 98.95%
CHEMBL1952 P04818 Thymidylate synthase 83.06% 93.53%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.81% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.20% 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 401304
LOTUS LTS0008667
wikiData Q82090193