Hydroxy-oxo-prop-2-enoxy-sulfanylidene-lambda6-sulfane

Details

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Internal ID 015181eb-807a-48ee-a113-efa100626aa5
Taxonomy Organic oxygen compounds > Organic oxoanionic compounds > Organic thiosulfates
IUPAC Name hydroxy-oxo-prop-2-enoxy-sulfanylidene-lambda6-sulfane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C3H6O3S2/c1-2-3-6-8(4,5)7/h2H,1,3H2,(H,4,5,7)
InChI Key FIDNEKIKYLOGTF-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C3H6O3S2
Molecular Weight 154.21 g/mol
Exact Mass 153.97583640 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 1.50
Atomic LogP (AlogP) 0.32
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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SCHEMBL484283

2D Structure

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2D Structure of Hydroxy-oxo-prop-2-enoxy-sulfanylidene-lambda6-sulfane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7954 79.54%
Caco-2 - 0.5697 56.97%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.4397 43.97%
OATP2B1 inhibitior - 0.8648 86.48%
OATP1B1 inhibitior + 0.9640 96.40%
OATP1B3 inhibitior + 0.9436 94.36%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9166 91.66%
P-glycoprotein inhibitior - 0.9813 98.13%
P-glycoprotein substrate - 0.9897 98.97%
CYP3A4 substrate - 0.6718 67.18%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7973 79.73%
CYP3A4 inhibition - 0.9657 96.57%
CYP2C9 inhibition - 0.8021 80.21%
CYP2C19 inhibition - 0.7755 77.55%
CYP2D6 inhibition - 0.9012 90.12%
CYP1A2 inhibition - 0.7913 79.13%
CYP2C8 inhibition - 0.9739 97.39%
CYP inhibitory promiscuity - 0.9037 90.37%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.6782 67.82%
Carcinogenicity (trinary) Non-required 0.6146 61.46%
Eye corrosion + 0.7146 71.46%
Eye irritation + 0.8818 88.18%
Skin irritation + 0.5138 51.38%
Skin corrosion + 0.7747 77.47%
Ames mutagenesis - 0.5337 53.37%
Human Ether-a-go-go-Related Gene inhibition - 0.7763 77.63%
Micronuclear + 0.8000 80.00%
Hepatotoxicity + 0.7036 70.36%
skin sensitisation + 0.5359 53.59%
Respiratory toxicity - 0.6667 66.67%
Reproductive toxicity - 0.8556 85.56%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.6285 62.85%
Acute Oral Toxicity (c) III 0.6961 69.61%
Estrogen receptor binding - 0.8503 85.03%
Androgen receptor binding - 0.8865 88.65%
Thyroid receptor binding - 0.8098 80.98%
Glucocorticoid receptor binding - 0.8665 86.65%
Aromatase binding - 0.8441 84.41%
PPAR gamma - 0.8347 83.47%
Honey bee toxicity - 0.4776 47.76%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9466 94.66%

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
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 89.67% 83.57%
CHEMBL2179 P04062 Beta-glucocerebrosidase 85.88% 85.31%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.40% 96.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.26% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.92% 96.09%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 80.39% 86.92%

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
Allium sativum

Cross-Links

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PubChem 11469380
LOTUS LTS0262385
wikiData Q104995633