(E)-1-Methylsulfanylsulfonylprop-1-ene

Details

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Internal ID d28912cd-1213-4915-bf5c-2a985a73562a
Taxonomy Organosulfur compounds > Sulfonyls
IUPAC Name (E)-1-methylsulfanylsulfonylprop-1-ene
SMILES (Canonical) CC=CS(=O)(=O)SC
SMILES (Isomeric) C/C=C/S(=O)(=O)SC
InChI InChI=1S/C4H8O2S2/c1-3-4-8(5,6)7-2/h3-4H,1-2H3/b4-3+
InChI Key CLEWYXVGMQSNOV-ONEGZZNKSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C4H8O2S2
Molecular Weight 152.20 g/mol
Exact Mass 151.99657184 g/mol
Topological Polar Surface Area (TPSA) 67.80 Ų
XlogP 0.80
Atomic LogP (AlogP) 1.21
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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117869-74-6
S-Methyl-1-propenethiosulfonate
CLEWYXVGMQSNOV-ONEGZZNKSA-N
4-(2-Amino-6-methoxy-9H-purin-9-yl)-2-cyclopenten-1-ol

2D Structure

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2D Structure of (E)-1-Methylsulfanylsulfonylprop-1-ene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9633 96.33%
Caco-2 + 0.6513 65.13%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.3873 38.73%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9381 93.81%
OATP1B3 inhibitior + 0.9471 94.71%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9429 94.29%
P-glycoprotein inhibitior - 0.9877 98.77%
P-glycoprotein substrate - 0.9763 97.63%
CYP3A4 substrate - 0.6833 68.33%
CYP2C9 substrate - 0.5993 59.93%
CYP2D6 substrate - 0.8706 87.06%
CYP3A4 inhibition - 0.9660 96.60%
CYP2C9 inhibition - 0.6231 62.31%
CYP2C19 inhibition - 0.5057 50.57%
CYP2D6 inhibition - 0.9017 90.17%
CYP1A2 inhibition - 0.5956 59.56%
CYP2C8 inhibition - 0.9818 98.18%
CYP inhibitory promiscuity - 0.8024 80.24%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6996 69.96%
Carcinogenicity (trinary) Non-required 0.6461 64.61%
Eye corrosion + 0.8966 89.66%
Eye irritation + 0.9428 94.28%
Skin irritation + 0.5794 57.94%
Skin corrosion + 0.8498 84.98%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7025 70.25%
Micronuclear + 0.8400 84.00%
Hepatotoxicity + 0.7680 76.80%
skin sensitisation + 0.6454 64.54%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.7778 77.78%
Mitochondrial toxicity - 0.6914 69.14%
Nephrotoxicity + 0.7846 78.46%
Acute Oral Toxicity (c) III 0.6149 61.49%
Estrogen receptor binding - 0.9256 92.56%
Androgen receptor binding - 0.7222 72.22%
Thyroid receptor binding - 0.8155 81.55%
Glucocorticoid receptor binding - 0.8735 87.35%
Aromatase binding - 0.8527 85.27%
PPAR gamma - 0.9179 91.79%
Honey bee toxicity - 0.5546 55.46%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.8429 84.29%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.78% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 88.31% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.34% 96.00%
CHEMBL284 P27487 Dipeptidyl peptidase IV 83.14% 95.69%
CHEMBL1907 P15144 Aminopeptidase N 80.35% 93.31%

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 macrostemon

Cross-Links

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PubChem 5352794
LOTUS LTS0133147
wikiData Q104963271