Hydroxy-prop-1-enyl-prop-1-enylsulfanylsulfanium

Details

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Internal ID 42fd60db-384a-4d11-811b-a9fc5b8c77d3
Taxonomy Organosulfur compounds > Sulfenyl compounds
IUPAC Name hydroxy-prop-1-enyl-prop-1-enylsulfanylsulfanium
SMILES (Canonical) CC=CS[S+](C=CC)O
SMILES (Isomeric) CC=CS[S+](C=CC)O
InChI InChI=1S/C6H11OS2/c1-3-5-8-9(7)6-4-2/h3-7H,1-2H3/q+1
InChI Key LZVBLYBKZZWNDK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C6H11OS2+
Molecular Weight 163.30 g/mol
Exact Mass 163.02513232 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.79
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Hydroxy-prop-1-enyl-prop-1-enylsulfanylsulfanium

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7864 78.64%
Caco-2 + 0.7540 75.40%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Lysosomes 0.3735 37.35%
OATP2B1 inhibitior - 0.8695 86.95%
OATP1B1 inhibitior + 0.9303 93.03%
OATP1B3 inhibitior + 0.9457 94.57%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9149 91.49%
P-glycoprotein inhibitior - 0.9776 97.76%
P-glycoprotein substrate - 0.9844 98.44%
CYP3A4 substrate - 0.6997 69.97%
CYP2C9 substrate - 0.8027 80.27%
CYP2D6 substrate - 0.8059 80.59%
CYP3A4 inhibition - 0.9312 93.12%
CYP2C9 inhibition - 0.7202 72.02%
CYP2C19 inhibition - 0.6803 68.03%
CYP2D6 inhibition - 0.8693 86.93%
CYP1A2 inhibition - 0.6848 68.48%
CYP2C8 inhibition - 0.9687 96.87%
CYP inhibitory promiscuity - 0.8504 85.04%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) + 0.7796 77.96%
Carcinogenicity (trinary) Non-required 0.6197 61.97%
Eye corrosion + 0.6370 63.70%
Eye irritation + 0.9249 92.49%
Skin irritation + 0.5079 50.79%
Skin corrosion + 0.5940 59.40%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6720 67.20%
Micronuclear + 0.6900 69.00%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation - 0.5792 57.92%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.8111 81.11%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.5946 59.46%
Acute Oral Toxicity (c) III 0.4604 46.04%
Estrogen receptor binding - 0.8045 80.45%
Androgen receptor binding - 0.8736 87.36%
Thyroid receptor binding - 0.7436 74.36%
Glucocorticoid receptor binding - 0.8222 82.22%
Aromatase binding - 0.8151 81.51%
PPAR gamma - 0.8856 88.56%
Honey bee toxicity - 0.8619 86.19%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.8077 80.77%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.69% 96.09%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 81.46% 83.57%

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 tuberosum

Cross-Links

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PubChem 25200944
LOTUS LTS0186094
wikiData Q105160153