Methyl propyl tetrasulphide

Details

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Internal ID d8ba07b3-b1bd-48a9-9fb1-b0e408443dd3
Taxonomy Organosulfur compounds > Sulfenyl compounds
IUPAC Name 1-(methyltetrasulfanyl)propane
SMILES (Canonical) CCCSSSSC
SMILES (Isomeric) CCCSSSSC
InChI InChI=1S/C4H10S4/c1-3-4-6-8-7-5-2/h3-4H2,1-2H3
InChI Key QQHQQGRHGUQYLO-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C4H10S4
Molecular Weight 186.40 g/mol
Exact Mass 185.96653501 g/mol
Topological Polar Surface Area (TPSA) 101.00 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.70
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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Methyl propyl tetrasulphide
87148-08-1
EINECS 289-302-3
DTXSID10236151
1-(methyltetrasulfanyl)propane
RefChem:818060
DTXCID10158642
289-302-3
1-METHYL-4-PROPYLTETRASULFANE
NS00124749

2D Structure

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2D Structure of Methyl propyl tetrasulphide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9815 98.15%
Caco-2 + 0.7243 72.43%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.4081 40.81%
OATP2B1 inhibitior - 0.8609 86.09%
OATP1B1 inhibitior + 0.9332 93.32%
OATP1B3 inhibitior + 0.9463 94.63%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9467 94.67%
P-glycoprotein inhibitior - 0.9744 97.44%
P-glycoprotein substrate - 0.9206 92.06%
CYP3A4 substrate - 0.7039 70.39%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7426 74.26%
CYP3A4 inhibition - 0.9758 97.58%
CYP2C9 inhibition - 0.8202 82.02%
CYP2C19 inhibition - 0.8115 81.15%
CYP2D6 inhibition - 0.8800 88.00%
CYP1A2 inhibition - 0.7353 73.53%
CYP2C8 inhibition - 0.9566 95.66%
CYP inhibitory promiscuity - 0.7980 79.80%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.6198 61.98%
Eye corrosion + 0.9040 90.40%
Eye irritation + 0.9732 97.32%
Skin irritation + 0.5854 58.54%
Skin corrosion - 0.8976 89.76%
Ames mutagenesis - 0.6954 69.54%
Human Ether-a-go-go-Related Gene inhibition - 0.6990 69.90%
Micronuclear - 0.7800 78.00%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation + 0.5677 56.77%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity + 0.6540 65.40%
Acute Oral Toxicity (c) III 0.5014 50.14%
Estrogen receptor binding - 0.7999 79.99%
Androgen receptor binding - 0.9176 91.76%
Thyroid receptor binding - 0.6272 62.72%
Glucocorticoid receptor binding - 0.9058 90.58%
Aromatase binding - 0.8889 88.89%
PPAR gamma - 0.8748 87.48%
Honey bee toxicity - 0.9034 90.34%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.7917 79.17%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.48% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 89.38% 89.63%
CHEMBL2581 P07339 Cathepsin D 88.52% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 84.25% 90.17%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.03% 97.25%

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.
Allium ampeloprasum
Allium cepa

Cross-Links

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PubChem 528709
LOTUS LTS0201558
wikiData Q83118061