3-Acetyloxy-2-aminopropanoic acid

Details

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Internal ID f17f6765-569d-4be4-8415-428c57441e1e
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids
IUPAC Name 3-acetyloxy-2-aminopropanoic acid
SMILES (Canonical) CC(=O)OCC(C(=O)O)N
SMILES (Isomeric) CC(=O)OCC(C(=O)O)N
InChI InChI=1S/C5H9NO4/c1-3(7)10-2-4(6)5(8)9/h4H,2,6H2,1H3,(H,8,9)
InChI Key VZXPDPZARILFQX-UHFFFAOYSA-N
Popularity 86 references in papers

Physical and Chemical Properties

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Molecular Formula C5H9NO4
Molecular Weight 147.13 g/mol
Exact Mass 147.05315777 g/mol
Topological Polar Surface Area (TPSA) 89.60 Ų
XlogP -3.50
Atomic LogP (AlogP) -1.04
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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O-Acetyl-DL-serine
3-acetyloxy-2-aminopropanoic acid
3-(acetyloxy)-2-aminopropanoic acid
Serine acetate ester
NSC-226230
o-Acetylserine #
(2S)-3-acetyloxy-2-aminopropanoic acid
NSC 16549
NSC-16549
O-acetyl-d,l-serine
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Acetyloxy-2-aminopropanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9542 95.42%
Caco-2 - 0.9726 97.26%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Lysosomes 0.5160 51.60%
OATP2B1 inhibitior - 0.8507 85.07%
OATP1B1 inhibitior + 0.9664 96.64%
OATP1B3 inhibitior + 0.9333 93.33%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9274 92.74%
P-glycoprotein inhibitior - 0.9863 98.63%
P-glycoprotein substrate - 0.9822 98.22%
CYP3A4 substrate - 0.7289 72.89%
CYP2C9 substrate - 0.6063 60.63%
CYP2D6 substrate - 0.8369 83.69%
CYP3A4 inhibition - 0.8822 88.22%
CYP2C9 inhibition - 0.9369 93.69%
CYP2C19 inhibition - 0.9515 95.15%
CYP2D6 inhibition - 0.9132 91.32%
CYP1A2 inhibition - 0.8483 84.83%
CYP2C8 inhibition - 0.9835 98.35%
CYP inhibitory promiscuity - 0.9947 99.47%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7200 72.00%
Carcinogenicity (trinary) Non-required 0.6636 66.36%
Eye corrosion - 0.9418 94.18%
Eye irritation - 0.5778 57.78%
Skin irritation - 0.7811 78.11%
Skin corrosion - 0.7472 74.72%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8700 87.00%
Micronuclear + 0.5800 58.00%
Hepatotoxicity + 0.6026 60.26%
skin sensitisation - 0.9567 95.67%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.6238 62.38%
Acute Oral Toxicity (c) III 0.5759 57.59%
Estrogen receptor binding - 0.8849 88.49%
Androgen receptor binding - 0.8412 84.12%
Thyroid receptor binding - 0.9380 93.80%
Glucocorticoid receptor binding - 0.8133 81.33%
Aromatase binding - 0.8787 87.87%
PPAR gamma - 0.9415 94.15%
Honey bee toxicity - 0.9531 95.31%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.9100 91.00%
Fish aquatic toxicity - 0.6368 63.68%

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 97.63% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 95.45% 83.82%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.61% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.07% 99.17%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 86.26% 92.29%
CHEMBL2581 P07339 Cathepsin D 85.38% 98.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.26% 97.21%

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.
Arabidopsis thaliana

Cross-Links

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PubChem 189
LOTUS LTS0014318
wikiData Q81986333