Allylthiosulfinsaure

Details

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Internal ID b365cb08-b88a-418c-9799-39478214f587
Taxonomy Organosulfur compounds > Allyl sulfur compounds
IUPAC Name hydroxy-prop-2-enyl-sulfanylidene-lambda4-sulfane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C3H6OS2/c1-2-3-6(4)5/h2H,1,3H2,(H,4,5)
InChI Key CWMAKUHNGGQLGT-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C3H6OS2
Molecular Weight 122.21 g/mol
Exact Mass 121.98600716 g/mol
Topological Polar Surface Area (TPSA) 71.50 Ų
XlogP 3.00
Atomic LogP (AlogP) 0.73
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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SCHEMBL3240865

2D Structure

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2D Structure of Allylthiosulfinsaure

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8718 87.18%
Caco-2 + 0.6754 67.54%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Lysosomes 0.3990 39.90%
OATP2B1 inhibitior - 0.8683 86.83%
OATP1B1 inhibitior + 0.9462 94.62%
OATP1B3 inhibitior + 0.9434 94.34%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9475 94.75%
P-glycoprotein inhibitior - 0.9853 98.53%
P-glycoprotein substrate - 0.9906 99.06%
CYP3A4 substrate - 0.7418 74.18%
CYP2C9 substrate - 0.8185 81.85%
CYP2D6 substrate - 0.7924 79.24%
CYP3A4 inhibition - 0.9452 94.52%
CYP2C9 inhibition - 0.8004 80.04%
CYP2C19 inhibition - 0.7434 74.34%
CYP2D6 inhibition - 0.8838 88.38%
CYP1A2 inhibition - 0.7295 72.95%
CYP2C8 inhibition - 0.9356 93.56%
CYP inhibitory promiscuity - 0.8383 83.83%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) + 0.7176 71.76%
Carcinogenicity (trinary) Non-required 0.6622 66.22%
Eye corrosion + 0.7305 73.05%
Eye irritation + 0.9421 94.21%
Skin irritation + 0.5068 50.68%
Skin corrosion + 0.7195 71.95%
Ames mutagenesis - 0.8000 80.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7525 75.25%
Micronuclear + 0.6900 69.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.5710 57.10%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity - 0.9222 92.22%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity + 0.5418 54.18%
Acute Oral Toxicity (c) III 0.5024 50.24%
Estrogen receptor binding - 0.8107 81.07%
Androgen receptor binding - 0.9486 94.86%
Thyroid receptor binding - 0.8039 80.39%
Glucocorticoid receptor binding - 0.7694 76.94%
Aromatase binding - 0.8810 88.10%
PPAR gamma - 0.8772 87.72%
Honey bee toxicity - 0.7698 76.98%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.6658 66.58%

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
No predicted targets yet!

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 ampeloprasum

Cross-Links

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PubChem 53743786
LOTUS LTS0203521
wikiData Q104971370