Homoserine lactone

Details

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Internal ID 5eb87b3c-9821-4688-9b00-f406cc0ec30a
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acid esters
IUPAC Name 3-aminooxolan-2-one
SMILES (Canonical) C1COC(=O)C1N
SMILES (Isomeric) C1COC(=O)C1N
InChI InChI=1S/C4H7NO2/c5-3-1-2-7-4(3)6/h3H,1-2,5H2
InChI Key QJPWUUJVYOJNMH-UHFFFAOYSA-N
Popularity 792 references in papers

Physical and Chemical Properties

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Molecular Formula C4H7NO2
Molecular Weight 101.10 g/mol
Exact Mass 101.047678466 g/mol
Topological Polar Surface Area (TPSA) 52.30 Ų
XlogP -0.60
Atomic LogP (AlogP) -0.74
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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1192-20-7
3-aminodihydrofuran-2(3H)-one
3-aminooxolan-2-one
2-Aminobutan-4-olide
171736-85-9
(S)-(-)-alpha-amino-gamma-butyrolactone hydroiodide
3-Aminodihydro-2(3H)-furanone
2(3H)-furanone, 3-aminodihydro-
HSL
Alpha-amino-gamma-butyrolactone
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Homoserine lactone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9927 99.27%
Caco-2 - 0.7707 77.07%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.7089 70.89%
OATP2B1 inhibitior - 0.8495 84.95%
OATP1B1 inhibitior + 0.9811 98.11%
OATP1B3 inhibitior + 0.9449 94.49%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9309 93.09%
P-glycoprotein inhibitior - 0.9907 99.07%
P-glycoprotein substrate - 0.9675 96.75%
CYP3A4 substrate - 0.7202 72.02%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7333 73.33%
CYP3A4 inhibition - 0.9663 96.63%
CYP2C9 inhibition - 0.9371 93.71%
CYP2C19 inhibition - 0.9001 90.01%
CYP2D6 inhibition - 0.9468 94.68%
CYP1A2 inhibition - 0.8081 80.81%
CYP2C8 inhibition - 0.9799 97.99%
CYP inhibitory promiscuity - 0.9695 96.95%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6533 65.33%
Eye corrosion - 0.8666 86.66%
Eye irritation + 0.8705 87.05%
Skin irritation - 0.6521 65.21%
Skin corrosion - 0.7521 75.21%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7534 75.34%
Micronuclear - 0.5700 57.00%
Hepatotoxicity + 0.8125 81.25%
skin sensitisation - 0.9133 91.33%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity + 0.6614 66.14%
Acute Oral Toxicity (c) III 0.5247 52.47%
Estrogen receptor binding - 0.9193 91.93%
Androgen receptor binding - 0.7676 76.76%
Thyroid receptor binding - 0.8998 89.98%
Glucocorticoid receptor binding - 0.8751 87.51%
Aromatase binding - 0.8927 89.27%
PPAR gamma - 0.9026 90.26%
Honey bee toxicity - 0.8591 85.91%
Biodegradation + 0.9000 90.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity - 0.9478 94.78%

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
CHEMBL3137262 O60341 LSD1/CoREST complex 93.74% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.44% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 84.96% 83.82%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.95% 95.56%
CHEMBL3384 Q16512 Protein kinase N1 82.18% 80.71%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.78% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.38% 95.89%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 73509
LOTUS LTS0014361
wikiData Q105222809