8-Methylsulfinyloctyl isothiocyanate

Details

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Internal ID 96cd684c-c206-41dc-a4eb-4d2714bdf14c
Taxonomy Organosulfur compounds > Sulfoxides
IUPAC Name 1-isothiocyanato-8-methylsulfinyloctane
SMILES (Canonical) CS(=O)CCCCCCCCN=C=S
SMILES (Isomeric) CS(=O)CCCCCCCCN=C=S
InChI InChI=1S/C10H19NOS2/c1-14(12)9-7-5-3-2-4-6-8-11-10-13/h2-9H2,1H3
InChI Key BCRXKWOQVFKZAG-UHFFFAOYSA-N
Popularity 18 references in papers

Physical and Chemical Properties

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Molecular Formula C10H19NOS2
Molecular Weight 233.40 g/mol
Exact Mass 233.09080658 g/mol
Topological Polar Surface Area (TPSA) 80.70 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.81
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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75272-81-0
8-(Methylsulfinyl)octyl isothiocyanate
1-isothiocyanato-8-methylsulfinyloctane
Octane, 1-isothiocyanato-8-(methylsulfinyl)-
1-isothiocyanato-8-(methylsulfinyl)octane
1-isothiocyanato-8-methanesulfinyloctane
Hirsutin?
8-MeSO-octyl-NCS
SCHEMBL2485837
CHEBI:91152
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 8-Methylsulfinyloctyl isothiocyanate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9211 92.11%
Caco-2 + 0.7470 74.70%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.6107 61.07%
OATP2B1 inhibitior - 0.8556 85.56%
OATP1B1 inhibitior + 0.9479 94.79%
OATP1B3 inhibitior + 0.9442 94.42%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior + 0.5250 52.50%
BSEP inhibitior - 0.7065 70.65%
P-glycoprotein inhibitior - 0.9653 96.53%
P-glycoprotein substrate - 0.8711 87.11%
CYP3A4 substrate - 0.5789 57.89%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7505 75.05%
CYP3A4 inhibition - 0.9640 96.40%
CYP2C9 inhibition - 0.8465 84.65%
CYP2C19 inhibition - 0.7712 77.12%
CYP2D6 inhibition - 0.8943 89.43%
CYP1A2 inhibition - 0.6948 69.48%
CYP2C8 inhibition - 0.9077 90.77%
CYP inhibitory promiscuity - 0.9395 93.95%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5378 53.78%
Carcinogenicity (trinary) Non-required 0.6236 62.36%
Eye corrosion - 0.6943 69.43%
Eye irritation + 0.8243 82.43%
Skin irritation - 0.5982 59.82%
Skin corrosion - 0.5706 57.06%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6702 67.02%
Micronuclear - 0.6300 63.00%
Hepatotoxicity + 0.5038 50.38%
skin sensitisation - 0.7507 75.07%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity - 0.8000 80.00%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.6589 65.89%
Acute Oral Toxicity (c) III 0.5197 51.97%
Estrogen receptor binding - 0.7458 74.58%
Androgen receptor binding - 0.8991 89.91%
Thyroid receptor binding - 0.5093 50.93%
Glucocorticoid receptor binding - 0.7086 70.86%
Aromatase binding - 0.8340 83.40%
PPAR gamma - 0.6772 67.72%
Honey bee toxicity - 0.7326 73.26%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.7200 72.00%
Fish aquatic toxicity - 0.6846 68.46%

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
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.78% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.57% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.08% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.36% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.21% 96.95%

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.
Arabidopsis thaliana
Rorippa sylvestris

Cross-Links

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PubChem 9794659
LOTUS LTS0123022
wikiData Q27163088