Alyssin

Details

Top
Internal ID 28aea219-58eb-4428-82ad-e734bbe617d5
Taxonomy Organosulfur compounds > Sulfoxides
IUPAC Name 1-isothiocyanato-5-methylsulfinylpentane
SMILES (Canonical) CS(=O)CCCCCN=C=S
SMILES (Isomeric) CS(=O)CCCCCN=C=S
InChI InChI=1S/C7H13NOS2/c1-11(9)6-4-2-3-5-8-7-10/h2-6H2,1H3
InChI Key IUUQPVQTAUKPPB-UHFFFAOYSA-N
Popularity 9 references in papers

Physical and Chemical Properties

Top
Molecular Formula C7H13NOS2
Molecular Weight 191.30 g/mol
Exact Mass 191.04385639 g/mol
Topological Polar Surface Area (TPSA) 80.70 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.64
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

Top
646-23-1
1-Isothiocyanato-5-(methylsulfinyl)pentane
Alyssin, (S)-
1-isothiocyanato-5-methylsulfinylpentane
Alyssin, (R)-
Pentane, 1-isothiocyanato-5-(methylsulfinyl)-
1-isothiocyanato-5-methanesulfinylpentane
CHEMBL4520951
5-Methylsulfinylpentylisothiocyanate
0929AF184M
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

Top
2D Structure of Alyssin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9211 92.11%
Caco-2 + 0.8604 86.04%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.6107 61.07%
OATP2B1 inhibitior - 0.8540 85.40%
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 - 0.9333 93.33%
P-glycoprotein inhibitior - 0.9752 97.52%
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 + 0.8030 80.30%
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 - 0.7089 70.89%
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 - 0.6712 67.12%
Androgen receptor binding - 0.9101 91.01%
Thyroid receptor binding - 0.6877 68.77%
Glucocorticoid receptor binding - 0.8492 84.92%
Aromatase binding - 0.7797 77.97%
PPAR gamma - 0.8623 86.23%
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

Top

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

Top
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.
Aurinia sinuata
Erysimum cuspidatum
Eutrema japonicum

Cross-Links

Top
PubChem 206035
LOTUS LTS0003591
wikiData Q27236447