Butyl p-tolyl sulfide

Details

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Internal ID 92c69432-e59d-4714-8e75-7feb8f6f9c0e
Taxonomy Organosulfur compounds > Thioethers > Aryl thioethers
IUPAC Name 1-butylsulfanyl-4-methylbenzene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H16S/c1-3-4-9-12-11-7-5-10(2)6-8-11/h5-8H,3-4,9H2,1-2H3
InChI Key FUYIIAJEXUJNFA-UHFFFAOYSA-N
Popularity 16 references in papers

Physical and Chemical Properties

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Molecular Formula C11H16S
Molecular Weight 180.31 g/mol
Exact Mass 180.09727168 g/mol
Topological Polar Surface Area (TPSA) 25.30 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.89
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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n-Butyl p-tolyl sulfide
4-Methyl-1-(1-thiapentyl)benzene
21784-96-3
Sulfide, butyl p-tolyl
4-(n-Butylthio)toluene
Benzene, 1-(butylthio)-4-methyl-
1-(Butylsulfanyl)-4-methylbenzene
SCHEMBL424971
n-Butyl 4-Methylphenyl Sulfide
DTXSID30944387
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Butyl p-tolyl sulfide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 + 0.9771 97.71%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.5954 59.54%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9396 93.96%
OATP1B3 inhibitior + 0.9455 94.55%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.7697 76.97%
P-glycoprotein inhibitior - 0.9781 97.81%
P-glycoprotein substrate - 0.8905 89.05%
CYP3A4 substrate - 0.6917 69.17%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3812 38.12%
CYP3A4 inhibition - 0.7565 75.65%
CYP2C9 inhibition - 0.6370 63.70%
CYP2C19 inhibition - 0.5646 56.46%
CYP2D6 inhibition - 0.7745 77.45%
CYP1A2 inhibition + 0.5802 58.02%
CYP2C8 inhibition - 0.8590 85.90%
CYP inhibitory promiscuity + 0.5560 55.60%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6500 65.00%
Carcinogenicity (trinary) Non-required 0.5787 57.87%
Eye corrosion + 0.8380 83.80%
Eye irritation + 0.9451 94.51%
Skin irritation + 0.6747 67.47%
Skin corrosion - 0.8527 85.27%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5115 51.15%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation + 0.8648 86.48%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.6778 67.78%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.6540 65.40%
Acute Oral Toxicity (c) III 0.8069 80.69%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding - 0.7007 70.07%
Thyroid receptor binding - 0.5436 54.36%
Glucocorticoid receptor binding - 0.8506 85.06%
Aromatase binding - 0.5443 54.43%
PPAR gamma - 0.6090 60.90%
Honey bee toxicity - 0.9767 97.67%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.7700 77.00%
Fish aquatic toxicity + 0.9916 99.16%

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 94.82% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.45% 96.09%
CHEMBL240 Q12809 HERG 84.08% 89.76%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 83.84% 92.08%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.66% 93.56%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.62% 95.56%
CHEMBL1907 P15144 Aminopeptidase N 83.13% 93.31%
CHEMBL3401 O75469 Pregnane X receptor 81.43% 94.73%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 80.93% 89.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.71% 99.17%

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.
Aegle marmelos

Cross-Links

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PubChem 304040
LOTUS LTS0006202
wikiData Q82921604