3-Isoxazolidinone

Details

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Internal ID f12335e7-fec7-43b4-8a65-5f9f96c34b53
Taxonomy Organoheterocyclic compounds > Azolidines > Oxazolidines > Oxazolidinones
IUPAC Name 1,2-oxazolidin-3-one
SMILES (Canonical) C1CONC1=O
SMILES (Isomeric) C1CONC1=O
InChI InChI=1S/C3H5NO2/c5-3-1-2-6-4-3/h1-2H2,(H,4,5)
InChI Key QXDOFVVNXBGLKK-UHFFFAOYSA-N
Popularity 96 references in papers

Physical and Chemical Properties

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Molecular Formula C3H5NO2
Molecular Weight 87.08 g/mol
Exact Mass 87.032028402 g/mol
Topological Polar Surface Area (TPSA) 38.30 Ų
XlogP -0.70
Atomic LogP (AlogP) -0.56
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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1192-07-0
3-Isoxazolidinone
1,2-oxazolidin-3-one
3-Isoxazolidone
isoxazolidinone
hydroxyisoxazoline
Isoxazolidine-3-one
DTXSID60152332
CHEBI:178224
QXDOFVVNXBGLKK-UHFFFAOYSA-N
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-Isoxazolidinone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.5508 55.08%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7857 78.57%
Subcellular localzation Mitochondria 0.5584 55.84%
OATP2B1 inhibitior - 0.8659 86.59%
OATP1B1 inhibitior + 0.9727 97.27%
OATP1B3 inhibitior + 0.9427 94.27%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9401 94.01%
P-glycoprotein inhibitior - 0.9865 98.65%
P-glycoprotein substrate - 0.9914 99.14%
CYP3A4 substrate - 0.7584 75.84%
CYP2C9 substrate - 0.8074 80.74%
CYP2D6 substrate - 0.8251 82.51%
CYP3A4 inhibition - 0.9946 99.46%
CYP2C9 inhibition - 0.8837 88.37%
CYP2C19 inhibition - 0.8718 87.18%
CYP2D6 inhibition - 0.8708 87.08%
CYP1A2 inhibition - 0.7639 76.39%
CYP2C8 inhibition - 0.9960 99.60%
CYP inhibitory promiscuity - 0.9738 97.38%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7300 73.00%
Carcinogenicity (trinary) Non-required 0.4239 42.39%
Eye corrosion - 0.9424 94.24%
Eye irritation + 0.9584 95.84%
Skin irritation - 0.7438 74.38%
Skin corrosion - 0.9179 91.79%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7476 74.76%
Micronuclear + 0.6000 60.00%
Hepatotoxicity + 0.8250 82.50%
skin sensitisation - 0.8563 85.63%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.5162 51.62%
Acute Oral Toxicity (c) III 0.5951 59.51%
Estrogen receptor binding - 0.8995 89.95%
Androgen receptor binding - 0.9622 96.22%
Thyroid receptor binding - 0.9061 90.61%
Glucocorticoid receptor binding - 0.9526 95.26%
Aromatase binding - 0.8554 85.54%
PPAR gamma - 0.8654 86.54%
Honey bee toxicity - 0.9148 91.48%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity - 0.9885 98.85%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.85% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.40% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.09% 94.45%
CHEMBL2581 P07339 Cathepsin D 82.60% 98.95%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 80.85% 93.40%

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.
Achillea erba-rotta subsp. moschata

Cross-Links

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PubChem 192737
NPASS NPC115772