Alanine, 3-(ethylsulfinyl)-

Details

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Internal ID 72bec03c-c22e-4b3c-b820-625a3dec6521
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids
IUPAC Name 2-amino-3-ethylsulfinylpropanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H11NO3S/c1-2-10(9)3-4(6)5(7)8/h4H,2-3,6H2,1H3,(H,7,8)
InChI Key CSZTZFUEOCFFJH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C5H11NO3S
Molecular Weight 165.21 g/mol
Exact Mass 165.04596439 g/mol
Topological Polar Surface Area (TPSA) 99.60 Ų
XlogP -4.00
Atomic LogP (AlogP) -0.83
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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Alanine, 3-(ethylsulfinyl)-
3-(Ethylsulfinyl)alanine, 9CI
SCHEMBL12086544
CHEBI:165858
2-amino-3-ethylsulinylpropanoic acid
AKOS014777944
2-amino-3-ethylsulfinyl-propanoic acid
2-amino-3-(ethanesulfinyl)propanoic acid

2D Structure

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2D Structure of Alanine, 3-(ethylsulfinyl)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8890 88.90%
Caco-2 - 0.8379 83.79%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Lysosomes 0.7208 72.08%
OATP2B1 inhibitior - 0.8563 85.63%
OATP1B1 inhibitior + 0.9435 94.35%
OATP1B3 inhibitior + 0.9403 94.03%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9044 90.44%
P-glycoprotein inhibitior - 0.9834 98.34%
P-glycoprotein substrate - 0.9532 95.32%
CYP3A4 substrate - 0.7640 76.40%
CYP2C9 substrate - 0.6141 61.41%
CYP2D6 substrate - 0.8250 82.50%
CYP3A4 inhibition - 0.8990 89.90%
CYP2C9 inhibition - 0.8795 87.95%
CYP2C19 inhibition - 0.8716 87.16%
CYP2D6 inhibition - 0.9168 91.68%
CYP1A2 inhibition - 0.8581 85.81%
CYP2C8 inhibition - 0.9732 97.32%
CYP inhibitory promiscuity - 0.9955 99.55%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5004 50.04%
Carcinogenicity (trinary) Non-required 0.6913 69.13%
Eye corrosion - 0.9314 93.14%
Eye irritation - 0.7968 79.68%
Skin irritation - 0.7719 77.19%
Skin corrosion - 0.8648 86.48%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7742 77.42%
Micronuclear + 0.7000 70.00%
Hepatotoxicity + 0.6400 64.00%
skin sensitisation - 0.8566 85.66%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.8166 81.66%
Acute Oral Toxicity (c) III 0.5954 59.54%
Estrogen receptor binding - 0.9062 90.62%
Androgen receptor binding - 0.8625 86.25%
Thyroid receptor binding - 0.9249 92.49%
Glucocorticoid receptor binding - 0.8463 84.63%
Aromatase binding - 0.9175 91.75%
PPAR gamma - 0.8511 85.11%
Honey bee toxicity - 0.9773 97.73%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.9200 92.00%
Fish aquatic toxicity - 0.6197 61.97%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.03% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 94.32% 96.95%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 92.71% 92.29%
CHEMBL4040 P28482 MAP kinase ERK2 91.11% 83.82%
CHEMBL2581 P07339 Cathepsin D 89.77% 98.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 87.82% 97.21%
CHEMBL221 P23219 Cyclooxygenase-1 86.12% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.68% 99.17%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 81.77% 100.00%

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.
Allium schoenoprasum
Tulbaghia violacea

Cross-Links

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PubChem 487523
LOTUS LTS0022212
wikiData Q104375956