S-Methyl 2-propene-1-sulfinothioate

Details

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Internal ID 567d28f2-8597-4070-9d20-58b8f6ec49fe
Taxonomy Organic acids and derivatives > Thiosulfinic acid esters
IUPAC Name 3-methylsulfanylsulfinylprop-1-ene
SMILES (Canonical) CSS(=O)CC=C
SMILES (Isomeric) CSS(=O)CC=C
InChI InChI=1S/C4H8OS2/c1-3-4-7(5)6-2/h3H,1,4H2,2H3
InChI Key ZIMQNNOENLFVMT-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C4H8OS2
Molecular Weight 136.20 g/mol
Exact Mass 136.00165722 g/mol
Topological Polar Surface Area (TPSA) 61.60 Ų
XlogP 0.70
Atomic LogP (AlogP) 1.20
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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3-methylsulfanylsulfinylprop-1-ene
3736-98-9
Methyl allylthiosulfinate
CHEMBL255815
SCHEMBL7034004
3-methylsulanylsulinylprop-1-ene
CHEBI:169722
DTXSID901296304
S-Methyl-2-propene-1-thiosulfinate
[(prop-2-ene-1-sulfinyl)sulfanyl]methane
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of S-Methyl 2-propene-1-sulfinothioate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9768 97.68%
Caco-2 + 0.6059 60.59%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.4331 43.31%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9486 94.86%
OATP1B3 inhibitior + 0.9441 94.41%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9471 94.71%
P-glycoprotein inhibitior - 0.9870 98.70%
P-glycoprotein substrate - 0.9802 98.02%
CYP3A4 substrate - 0.6812 68.12%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8022 80.22%
CYP3A4 inhibition - 0.9668 96.68%
CYP2C9 inhibition - 0.7261 72.61%
CYP2C19 inhibition - 0.6656 66.56%
CYP2D6 inhibition - 0.8873 88.73%
CYP1A2 inhibition - 0.6454 64.54%
CYP2C8 inhibition - 0.9480 94.80%
CYP inhibitory promiscuity - 0.8116 81.16%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6540 65.40%
Carcinogenicity (trinary) Non-required 0.6522 65.22%
Eye corrosion + 0.6019 60.19%
Eye irritation + 0.8623 86.23%
Skin irritation - 0.5327 53.27%
Skin corrosion - 0.5643 56.43%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7455 74.55%
Micronuclear + 0.6700 67.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.5736 57.36%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.7813 78.13%
Acute Oral Toxicity (c) III 0.5173 51.73%
Estrogen receptor binding - 0.8509 85.09%
Androgen receptor binding - 0.9223 92.23%
Thyroid receptor binding - 0.8251 82.51%
Glucocorticoid receptor binding - 0.8928 89.28%
Aromatase binding - 0.8690 86.90%
PPAR gamma - 0.9309 93.09%
Honey bee toxicity - 0.5283 52.83%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.8458 84.58%

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
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.39% 89.34%
CHEMBL2581 P07339 Cathepsin D 82.93% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.63% 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.
Allium sativum
Allium tuberosum
Allium ursinum

Cross-Links

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PubChem 5319504
NPASS NPC46648
ChEMBL CHEMBL255815
LOTUS LTS0214069
wikiData Q105377356