S-1-Propenyl 2-propenesulfinothioate

Details

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Internal ID 998f1d90-bedd-41b7-a4f1-6458a7dc63a9
Taxonomy Organic acids and derivatives > Thiosulfinic acid esters
IUPAC Name (E)-1-prop-2-enylsulfinylsulfanylprop-1-ene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H10OS2/c1-3-5-8-9(7)6-4-2/h3-5H,2,6H2,1H3/b5-3+
InChI Key UALJWNWDDJRJTL-HWKANZROSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C6H10OS2
Molecular Weight 162.30 g/mol
Exact Mass 162.01730729 g/mol
Topological Polar Surface Area (TPSA) 61.60 Ų
XlogP 1.40
Atomic LogP (AlogP) 2.10
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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Allyl-SS(O)-Propenyl
SCHEMBL7030690
SCHEMBL7031678
DTXSID901242602
134568-42-6
S-(1E)-1-Propen-1-yl 2-propene-1-sulfinothioate
(1E)-1-[(prop-2-ene-1-sulfinyl)sulfanyl]prop-1-ene

2D Structure

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2D Structure of S-1-Propenyl 2-propenesulfinothioate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9749 97.49%
Caco-2 + 0.5979 59.79%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.3903 39.03%
OATP2B1 inhibitior - 0.8681 86.81%
OATP1B1 inhibitior + 0.9045 90.45%
OATP1B3 inhibitior + 0.9453 94.53%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9384 93.84%
P-glycoprotein inhibitior - 0.9754 97.54%
P-glycoprotein substrate - 0.9684 96.84%
CYP3A4 substrate - 0.6542 65.42%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8278 82.78%
CYP3A4 inhibition - 0.9175 91.75%
CYP2C9 inhibition - 0.7014 70.14%
CYP2C19 inhibition - 0.6589 65.89%
CYP2D6 inhibition - 0.8821 88.21%
CYP1A2 inhibition - 0.6516 65.16%
CYP2C8 inhibition - 0.9166 91.66%
CYP inhibitory promiscuity - 0.6997 69.97%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6540 65.40%
Carcinogenicity (trinary) Non-required 0.5941 59.41%
Eye corrosion + 0.7764 77.64%
Eye irritation + 0.6631 66.31%
Skin irritation - 0.5260 52.60%
Skin corrosion + 0.6164 61.64%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6525 65.25%
Micronuclear + 0.6900 69.00%
Hepatotoxicity + 0.6875 68.75%
skin sensitisation - 0.5374 53.74%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.9333 93.33%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.7949 79.49%
Acute Oral Toxicity (c) III 0.5506 55.06%
Estrogen receptor binding - 0.8357 83.57%
Androgen receptor binding - 0.9047 90.47%
Thyroid receptor binding - 0.6663 66.63%
Glucocorticoid receptor binding - 0.7911 79.11%
Aromatase binding - 0.8094 80.94%
PPAR gamma - 0.7912 79.12%
Honey bee toxicity - 0.5801 58.01%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.8493 84.93%

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 85.25% 96.09%
CHEMBL2581 P07339 Cathepsin D 84.49% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 83.89% 89.34%

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 ursinum

Cross-Links

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PubChem 10558949
LOTUS LTS0097985
wikiData Q105268880