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) C=CCOS(=O)(=S)O
SMILES (Isomeric) C=CCOS(=O)(=S)O
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 1 reference 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

Synonyms

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There are no found synonyms.

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 (%)
No predicted properties yet!

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