1-Prop-1-enylsulfanylsulfinylpropane

Details

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Internal ID 6f7766d4-cfb4-49ee-9ece-8acc1efe974d
Taxonomy Organic acids and derivatives > Thiosulfinic acid esters
IUPAC Name 1-prop-1-enylsulfanylsulfinylpropane
SMILES (Canonical) CCCS(=O)SC=CC
SMILES (Isomeric) CCCS(=O)SC=CC
InChI InChI=1S/C6H12OS2/c1-3-5-8-9(7)6-4-2/h3,5H,4,6H2,1-2H3
InChI Key XLVMWOFYTFNDKM-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C6H12OS2
Molecular Weight 164.30 g/mol
Exact Mass 164.03295735 g/mol
Topological Polar Surface Area (TPSA) 61.60 Ų
XlogP 1.50
Atomic LogP (AlogP) 2.33
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-Prop-1-enylsulfanylsulfinylpropane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9829 98.29%
Caco-2 + 0.8610 86.10%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Plasma membrane 0.4176 41.76%
OATP2B1 inhibitior - 0.8593 85.93%
OATP1B1 inhibitior + 0.8801 88.01%
OATP1B3 inhibitior + 0.9423 94.23%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9128 91.28%
P-glycoprotein inhibitior - 0.9793 97.93%
P-glycoprotein substrate - 0.9449 94.49%
CYP3A4 substrate - 0.6912 69.12%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8018 80.18%
CYP3A4 inhibition - 0.9243 92.43%
CYP2C9 inhibition - 0.7116 71.16%
CYP2C19 inhibition - 0.7094 70.94%
CYP2D6 inhibition - 0.8932 89.32%
CYP1A2 inhibition - 0.6778 67.78%
CYP2C8 inhibition - 0.9211 92.11%
CYP inhibitory promiscuity - 0.6763 67.63%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6096 60.96%
Carcinogenicity (trinary) Non-required 0.6170 61.70%
Eye corrosion + 0.6314 63.14%
Eye irritation + 0.9656 96.56%
Skin irritation - 0.6240 62.40%
Skin corrosion - 0.7048 70.48%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6988 69.88%
Micronuclear + 0.5100 51.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation + 0.4924 49.24%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.7143 71.43%
Acute Oral Toxicity (c) III 0.5088 50.88%
Estrogen receptor binding - 0.8898 88.98%
Androgen receptor binding - 0.8812 88.12%
Thyroid receptor binding - 0.6478 64.78%
Glucocorticoid receptor binding - 0.8837 88.37%
Aromatase binding - 0.8708 87.08%
PPAR gamma - 0.8653 86.53%
Honey bee toxicity - 0.8277 82.77%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.8377 83.77%

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 89.12% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.64% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.83% 96.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.98% 89.34%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.92% 97.21%

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 cepa

Cross-Links

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PubChem 72731117
LOTUS LTS0029552
wikiData Q105330440