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

Details

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Internal ID ef1e2d82-1740-4a2d-90f4-f3f66ea6c271
Taxonomy Organosulfur compounds > Sulfoxides
IUPAC Name N-(2-hydroxyethyl)-3-methylsulfinylprop-2-enamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H11NO3S/c1-11(10)5-2-6(9)7-3-4-8/h2,5,8H,3-4H2,1H3,(H,7,9)
InChI Key LBGAGBWSXXFWGZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C6H11NO3S
Molecular Weight 177.22 g/mol
Exact Mass 177.04596439 g/mol
Topological Polar Surface Area (TPSA) 85.60 Ų
XlogP -1.80
Atomic LogP (AlogP) -1.01
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of N-(2-hydroxyethyl)-3-methylsulfinylprop-2-enamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7516 75.16%
Caco-2 + 0.6030 60.30%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.5509 55.09%
OATP2B1 inhibitior - 0.8589 85.89%
OATP1B1 inhibitior + 0.9245 92.45%
OATP1B3 inhibitior + 0.9446 94.46%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9395 93.95%
P-glycoprotein inhibitior - 0.9754 97.54%
P-glycoprotein substrate - 0.7460 74.60%
CYP3A4 substrate - 0.6304 63.04%
CYP2C9 substrate - 0.8052 80.52%
CYP2D6 substrate - 0.8563 85.63%
CYP3A4 inhibition - 0.8500 85.00%
CYP2C9 inhibition - 0.8248 82.48%
CYP2C19 inhibition - 0.8331 83.31%
CYP2D6 inhibition - 0.9284 92.84%
CYP1A2 inhibition - 0.8475 84.75%
CYP2C8 inhibition - 0.9465 94.65%
CYP inhibitory promiscuity - 0.9741 97.41%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) + 0.5388 53.88%
Carcinogenicity (trinary) Non-required 0.6641 66.41%
Eye corrosion - 0.9354 93.54%
Eye irritation + 0.7783 77.83%
Skin irritation - 0.7691 76.91%
Skin corrosion - 0.9133 91.33%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8271 82.71%
Micronuclear + 0.6100 61.00%
Hepatotoxicity - 0.6584 65.84%
skin sensitisation - 0.8796 87.96%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.6889 68.89%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.5474 54.74%
Acute Oral Toxicity (c) III 0.5593 55.93%
Estrogen receptor binding - 0.8969 89.69%
Androgen receptor binding - 0.8438 84.38%
Thyroid receptor binding - 0.7954 79.54%
Glucocorticoid receptor binding - 0.8555 85.55%
Aromatase binding - 0.8087 80.87%
PPAR gamma - 0.7629 76.29%
Honey bee toxicity - 0.9218 92.18%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.8500 85.00%
Fish aquatic toxicity - 0.9533 95.33%

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
CHEMBL4040 P28482 MAP kinase ERK2 95.56% 83.82%
CHEMBL2581 P07339 Cathepsin D 89.73% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.63% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.86% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.68% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 80.94% 97.29%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.64% 94.33%

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.
Clinacanthus nutans
Entada phaseoloides

Cross-Links

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PubChem 85595979
LOTUS LTS0100957
wikiData Q105149243