Methylthiomethyl phenyl sulfone

Details

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Internal ID 85f18272-f282-4921-942e-381d44634f7f
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzenesulfonyl compounds
IUPAC Name methylsulfanylmethylsulfonylbenzene
SMILES (Canonical) CSCS(=O)(=O)C1=CC=CC=C1
SMILES (Isomeric) CSCS(=O)(=O)C1=CC=CC=C1
InChI InChI=1S/C8H10O2S2/c1-11-7-12(9,10)8-5-3-2-4-6-8/h2-6H,7H2,1H3
InChI Key XBGGZYQBIQAYII-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C8H10O2S2
Molecular Weight 202.30 g/mol
Exact Mass 202.01222190 g/mol
Topological Polar Surface Area (TPSA) 67.80 Ų
XlogP 1.90
Atomic LogP (AlogP) 1.78
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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59431-14-0
methylsulfanylmethylsulfonylbenzene
Methyl((phenylsulfonyl)methyl)sulfane
SCHEMBL730444
DTXSID00349143
XBGGZYQBIQAYII-UHFFFAOYSA-N
{[(methylthio)methyl]sulfonyl}benzene
1-((Methylthio)methylsulfonyl)benzene
Methylthiomethyl phenyl sulfone, 99%
AKOS024370876
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Methylthiomethyl phenyl sulfone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9723 97.23%
Caco-2 + 0.7880 78.80%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.3537 35.37%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9524 95.24%
OATP1B3 inhibitior + 0.9449 94.49%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9058 90.58%
P-glycoprotein inhibitior - 0.9842 98.42%
P-glycoprotein substrate - 0.9650 96.50%
CYP3A4 substrate - 0.7350 73.50%
CYP2C9 substrate - 0.7698 76.98%
CYP2D6 substrate - 0.7613 76.13%
CYP3A4 inhibition - 0.9437 94.37%
CYP2C9 inhibition - 0.5463 54.63%
CYP2C19 inhibition + 0.5487 54.87%
CYP2D6 inhibition - 0.8731 87.31%
CYP1A2 inhibition - 0.5483 54.83%
CYP2C8 inhibition - 0.8719 87.19%
CYP inhibitory promiscuity - 0.7776 77.76%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6051 60.51%
Carcinogenicity (trinary) Non-required 0.6221 62.21%
Eye corrosion + 0.6082 60.82%
Eye irritation + 0.9396 93.96%
Skin irritation - 0.6568 65.68%
Skin corrosion - 0.7546 75.46%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8241 82.41%
Micronuclear + 0.6900 69.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.6898 68.98%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.6435 64.35%
Acute Oral Toxicity (c) III 0.7083 70.83%
Estrogen receptor binding - 0.8244 82.44%
Androgen receptor binding - 0.9145 91.45%
Thyroid receptor binding - 0.8342 83.42%
Glucocorticoid receptor binding - 0.9519 95.19%
Aromatase binding - 0.7948 79.48%
PPAR gamma - 0.8729 87.29%
Honey bee toxicity - 0.9549 95.49%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.8713 87.13%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.86% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.85% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 89.98% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.86% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.35% 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 643313
LOTUS LTS0158556
wikiData Q82124219