Isoxazole-4-carboxylic acid

Details

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Internal ID a915b366-c3ce-45e3-a5b6-8e77e5088ebb
Taxonomy Organoheterocyclic compounds > Azoles > Isoxazoles
IUPAC Name 1,2-oxazole-4-carboxylic acid
SMILES (Canonical) C1=C(C=NO1)C(=O)O
SMILES (Isomeric) C1=C(C=NO1)C(=O)O
InChI InChI=1S/C4H3NO3/c6-4(7)3-1-5-8-2-3/h1-2H,(H,6,7)
InChI Key LYPXTDXYEQEIIN-UHFFFAOYSA-N
Popularity 15 references in papers

Physical and Chemical Properties

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Molecular Formula C4H3NO3
Molecular Weight 113.07 g/mol
Exact Mass 113.011292958 g/mol
Topological Polar Surface Area (TPSA) 63.30 Ų
XlogP -0.10
Atomic LogP (AlogP) 0.37
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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6436-62-0
4-Isoxazolecarboxylic acid
Isooxazole-4-carboxylic acid
1,2-oxazole-4-carboxylic acid
MFCD06738806
Isoxazole-4-carboxylicacid
4-carboxy isoxazole
SCHEMBL264004
DTXSID30214577
LYPXTDXYEQEIIN-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 Isoxazole-4-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9846 98.46%
Caco-2 - 0.5294 52.94%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.6344 63.44%
OATP2B1 inhibitior - 0.8749 87.49%
OATP1B1 inhibitior + 0.9461 94.61%
OATP1B3 inhibitior + 0.9528 95.28%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9541 95.41%
P-glycoprotein inhibitior - 0.9808 98.08%
P-glycoprotein substrate - 0.9896 98.96%
CYP3A4 substrate - 0.8063 80.63%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9048 90.48%
CYP3A4 inhibition - 0.9684 96.84%
CYP2C9 inhibition - 0.9243 92.43%
CYP2C19 inhibition - 0.8555 85.55%
CYP2D6 inhibition - 0.9243 92.43%
CYP1A2 inhibition - 0.6084 60.84%
CYP2C8 inhibition - 0.8576 85.76%
CYP inhibitory promiscuity - 0.9822 98.22%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.4771 47.71%
Eye corrosion - 0.7874 78.74%
Eye irritation + 0.9848 98.48%
Skin irritation - 0.6104 61.04%
Skin corrosion - 0.8808 88.08%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8659 86.59%
Micronuclear - 0.5700 57.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.8078 80.78%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.5880 58.80%
Acute Oral Toxicity (c) III 0.4861 48.61%
Estrogen receptor binding - 0.9249 92.49%
Androgen receptor binding - 0.9215 92.15%
Thyroid receptor binding - 0.8648 86.48%
Glucocorticoid receptor binding - 0.9234 92.34%
Aromatase binding - 0.8120 81.20%
PPAR gamma - 0.8975 89.75%
Honey bee toxicity - 0.9615 96.15%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.8300 83.00%
Fish aquatic toxicity - 0.7185 71.85%

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
CHEMBL1293277 O15118 Niemann-Pick C1 protein 96.47% 81.11%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 96.40% 87.67%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.45% 89.34%
CHEMBL1811 P34995 Prostanoid EP1 receptor 86.83% 95.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.51% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.28% 99.23%

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 3014488
LOTUS LTS0228924
wikiData Q72486670