Propyl 1-propenyl tetrasulfide

Details

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Internal ID 8485a5e1-ea59-4c88-958b-403e0b9e53cd
Taxonomy Organosulfur compounds > Sulfenyl compounds
IUPAC Name 1-[[(E)-prop-1-enyl]tetrasulfanyl]propane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H12S4/c1-3-5-7-9-10-8-6-4-2/h3,5H,4,6H2,1-2H3/b5-3+
InChI Key RKTJCWCBNXCDDQ-HWKANZROSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C6H12S4
Molecular Weight 212.40 g/mol
Exact Mass 211.98218508 g/mol
Topological Polar Surface Area (TPSA) 101.00 Ų
XlogP 3.40
Atomic LogP (AlogP) 4.61
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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Propyl 1-propenyl tetrasulfide, (E)-
RKTJCWCBNXCDDQ-HWKANZROSA-N
RKTJCWCBNXCDDQ-UHFFFAOYSA-N
Propyl (E)-1-propenyl tetrasulfide

2D Structure

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2D Structure of Propyl 1-propenyl tetrasulfide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9869 98.69%
Caco-2 + 0.7914 79.14%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.3414 34.14%
OATP2B1 inhibitior - 0.8642 86.42%
OATP1B1 inhibitior + 0.8813 88.13%
OATP1B3 inhibitior + 0.9434 94.34%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8810 88.10%
P-glycoprotein inhibitior - 0.9741 97.41%
P-glycoprotein substrate - 0.8996 89.96%
CYP3A4 substrate - 0.6597 65.97%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7555 75.55%
CYP3A4 inhibition - 0.9393 93.93%
CYP2C9 inhibition - 0.7848 78.48%
CYP2C19 inhibition - 0.7764 77.64%
CYP2D6 inhibition - 0.8684 86.84%
CYP1A2 inhibition - 0.6609 66.09%
CYP2C8 inhibition - 0.9398 93.98%
CYP inhibitory promiscuity - 0.6005 60.05%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6300 63.00%
Carcinogenicity (trinary) Non-required 0.5354 53.54%
Eye corrosion + 0.9003 90.03%
Eye irritation + 0.9481 94.81%
Skin irritation + 0.5986 59.86%
Skin corrosion - 0.8552 85.52%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6884 68.84%
Micronuclear - 0.7800 78.00%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation + 0.7030 70.30%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity + 0.4791 47.91%
Acute Oral Toxicity (c) III 0.6728 67.28%
Estrogen receptor binding - 0.7669 76.69%
Androgen receptor binding - 0.9203 92.03%
Thyroid receptor binding + 0.5430 54.30%
Glucocorticoid receptor binding - 0.7522 75.22%
Aromatase binding - 0.9111 91.11%
PPAR gamma - 0.5762 57.62%
Honey bee toxicity - 0.8339 83.39%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9549 95.49%

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 90.76% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.45% 98.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.93% 97.21%
CHEMBL221 P23219 Cyclooxygenase-1 84.56% 90.17%
CHEMBL226 P30542 Adenosine A1 receptor 82.49% 95.93%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.88% 89.34%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 5352692
NPASS NPC241724