N-(2-hydroxyethyl)-3-methylsulfanylprop-2-enamide

Details

Top
Internal ID 14f7161a-e66e-4f6e-8bed-b0899ce85ca0
Taxonomy Organosulfur compounds > Thioethers > Thioenol ethers
IUPAC Name N-(2-hydroxyethyl)-3-methylsulfanylprop-2-enamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H11NO2S/c1-10-5-2-6(9)7-3-4-8/h2,5,8H,3-4H2,1H3,(H,7,9)
InChI Key NBRCIHAGNJRRRI-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

Top
Molecular Formula C6H11NO2S
Molecular Weight 161.22 g/mol
Exact Mass 161.05104977 g/mol
Topological Polar Surface Area (TPSA) 74.60 Ų
XlogP -0.40
Atomic LogP (AlogP) -0.03
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of N-(2-hydroxyethyl)-3-methylsulfanylprop-2-enamide

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9536 95.36%
Caco-2 + 0.7565 75.65%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.5278 52.78%
OATP2B1 inhibitior - 0.8582 85.82%
OATP1B1 inhibitior + 0.9253 92.53%
OATP1B3 inhibitior + 0.9484 94.84%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9426 94.26%
P-glycoprotein inhibitior - 0.9829 98.29%
P-glycoprotein substrate - 0.7929 79.29%
CYP3A4 substrate - 0.6355 63.55%
CYP2C9 substrate - 0.6022 60.22%
CYP2D6 substrate - 0.8563 85.63%
CYP3A4 inhibition - 0.9224 92.24%
CYP2C9 inhibition - 0.8710 87.10%
CYP2C19 inhibition - 0.8467 84.67%
CYP2D6 inhibition - 0.9578 95.78%
CYP1A2 inhibition - 0.6928 69.28%
CYP2C8 inhibition - 0.9594 95.94%
CYP inhibitory promiscuity - 0.9578 95.78%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.6851 68.51%
Eye corrosion - 0.7186 71.86%
Eye irritation + 0.9315 93.15%
Skin irritation - 0.7955 79.55%
Skin corrosion - 0.9166 91.66%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7254 72.54%
Micronuclear - 0.6600 66.00%
Hepatotoxicity - 0.5090 50.90%
skin sensitisation - 0.9310 93.10%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.7333 73.33%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.6119 61.19%
Acute Oral Toxicity (c) III 0.6446 64.46%
Estrogen receptor binding - 0.9164 91.64%
Androgen receptor binding - 0.8258 82.58%
Thyroid receptor binding - 0.7175 71.75%
Glucocorticoid receptor binding - 0.8494 84.94%
Aromatase binding - 0.8031 80.31%
PPAR gamma - 0.7938 79.38%
Honey bee toxicity - 0.9284 92.84%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity - 0.9908 99.08%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.44% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.94% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 85.65% 89.34%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.43% 99.17%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.15% 94.33%

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.
Clinacanthus nutans

Cross-Links

Top
PubChem 130463
LOTUS LTS0273502
wikiData Q105176948