Oxaluric acid

Details

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Internal ID 08fb0320-f7fe-4180-b8a4-eff7006f5c33
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > N-carbamoyl-alpha amino acids and derivatives > N-carbamoyl-alpha amino acids
IUPAC Name 2-(carbamoylamino)-2-oxoacetic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C3H4N2O4/c4-3(9)5-1(6)2(7)8/h(H,7,8)(H3,4,5,6,9)
InChI Key UWBHMRBRLOJJAA-UHFFFAOYSA-N
Popularity 71 references in papers

Physical and Chemical Properties

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Molecular Formula C3H4N2O4
Molecular Weight 132.08 g/mol
Exact Mass 132.01710661 g/mol
Topological Polar Surface Area (TPSA) 109.00 Ų
XlogP -0.70
Atomic LogP (AlogP) -1.73
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

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585-05-7
oxalureate
Monooxalylurea
2-(carbamoylamino)-2-oxoacetic acid
ureido(oxo)acetic acid
carbamoylamino(oxo)acetic acid
CHEBI:16582
DTXSID00207214
RefChem:928344
DTXCID00129705
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Oxaluric acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6846 68.46%
Caco-2 - 0.7985 79.85%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.6798 67.98%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9752 97.52%
OATP1B3 inhibitior + 0.9496 94.96%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9862 98.62%
P-glycoprotein inhibitior - 0.9836 98.36%
P-glycoprotein substrate - 0.9787 97.87%
CYP3A4 substrate - 0.7757 77.57%
CYP2C9 substrate + 0.5955 59.55%
CYP2D6 substrate - 0.8844 88.44%
CYP3A4 inhibition - 0.8901 89.01%
CYP2C9 inhibition - 0.9361 93.61%
CYP2C19 inhibition - 0.9444 94.44%
CYP2D6 inhibition - 0.9367 93.67%
CYP1A2 inhibition - 0.9428 94.28%
CYP2C8 inhibition - 0.9862 98.62%
CYP inhibitory promiscuity - 1.0000 100.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7366 73.66%
Carcinogenicity (trinary) Non-required 0.7191 71.91%
Eye corrosion - 0.9879 98.79%
Eye irritation + 0.8741 87.41%
Skin irritation - 0.7061 70.61%
Skin corrosion - 0.9790 97.90%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8026 80.26%
Micronuclear + 0.7700 77.00%
Hepatotoxicity + 0.7375 73.75%
skin sensitisation - 0.9235 92.35%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity + 0.5549 55.49%
Acute Oral Toxicity (c) IV 0.4985 49.85%
Estrogen receptor binding - 0.9350 93.50%
Androgen receptor binding - 0.9339 93.39%
Thyroid receptor binding - 0.7176 71.76%
Glucocorticoid receptor binding - 0.7694 76.94%
Aromatase binding - 0.8062 80.62%
PPAR gamma - 0.6972 69.72%
Honey bee toxicity - 0.9587 95.87%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.9200 92.00%
Fish aquatic toxicity - 0.8330 83.30%

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
CHEMBL4040 P28482 MAP kinase ERK2 93.78% 83.82%
CHEMBL221 P23219 Cyclooxygenase-1 83.72% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.63% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.89% 91.11%

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 456
LOTUS LTS0079289
wikiData Q27101984