methyl N-(4-methylsulfanylbut-3-enyl)carbamodithioate

Details

Top
Internal ID 477b3110-5994-403a-a5c5-34b1117cec1d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Hemiacetals
IUPAC Name methyl N-(4-methylsulfanylbut-3-enyl)carbamodithioate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H13NS3/c1-10-6-4-3-5-8-7(9)11-2/h4,6H,3,5H2,1-2H3,(H,8,9)
InChI Key QBIPIEGWMMKSHS-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C7H13NS3
Molecular Weight 207.40 g/mol
Exact Mass 207.02101294 g/mol
Topological Polar Surface Area (TPSA) 94.70 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.49
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of methyl N-(4-methylsulfanylbut-3-enyl)carbamodithioate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9861 98.61%
Caco-2 + 0.7097 70.97%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Lysosomes 0.8437 84.37%
OATP2B1 inhibitior - 0.8579 85.79%
OATP1B1 inhibitior + 0.9305 93.05%
OATP1B3 inhibitior + 0.9460 94.60%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8380 83.80%
P-glycoprotein inhibitior - 0.9817 98.17%
P-glycoprotein substrate - 0.8291 82.91%
CYP3A4 substrate - 0.6107 61.07%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7493 74.93%
CYP3A4 inhibition - 0.9209 92.09%
CYP2C9 inhibition - 0.7825 78.25%
CYP2C19 inhibition - 0.5099 50.99%
CYP2D6 inhibition - 0.8438 84.38%
CYP1A2 inhibition + 0.6081 60.81%
CYP2C8 inhibition - 0.9595 95.95%
CYP inhibitory promiscuity - 0.5539 55.39%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.5670 56.70%
Eye corrosion + 0.5387 53.87%
Eye irritation + 0.5881 58.81%
Skin irritation + 0.6178 61.78%
Skin corrosion + 0.7436 74.36%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4286 42.86%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation - 0.5461 54.61%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.8000 80.00%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.4768 47.68%
Acute Oral Toxicity (c) II 0.4963 49.63%
Estrogen receptor binding - 0.7301 73.01%
Androgen receptor binding - 0.8820 88.20%
Thyroid receptor binding - 0.6324 63.24%
Glucocorticoid receptor binding - 0.7443 74.43%
Aromatase binding - 0.7949 79.49%
PPAR gamma - 0.5710 57.10%
Honey bee toxicity - 0.8249 82.49%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity - 0.7841 78.41%

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
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.16% 89.34%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.51% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.10% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.87% 99.17%
CHEMBL2581 P07339 Cathepsin D 80.80% 98.95%
CHEMBL226 P30542 Adenosine A1 receptor 80.35% 95.93%

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.
There are no matching plants.

Cross-Links

Top
PubChem 86163577
LOTUS LTS0106722
wikiData Q105217819