CID 20054975

Details

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Internal ID 380284f4-2fcc-4af2-a8a1-d8c737ce6514
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids > D-alpha-amino acids
IUPAC Name (2R)-2-azaniumyl-2-(2-oxo-3H-1,3-oxazol-5-yl)acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H6N2O4/c6-3(4(8)9)2-1-7-5(10)11-2/h1,3H,6H2,(H,7,10)(H,8,9)/t3-/m1/s1
InChI Key ASBGWPLVVIASBE-GSVOUGTGSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C5H6N2O4
Molecular Weight 158.11 g/mol
Exact Mass 158.03275668 g/mol
Topological Polar Surface Area (TPSA) 106.00 Ų
XlogP -3.20
Atomic LogP (AlogP) -3.00
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 20054975

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8551 85.51%
Caco-2 - 0.9403 94.03%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.5105 51.05%
OATP2B1 inhibitior - 0.8645 86.45%
OATP1B1 inhibitior + 0.9294 92.94%
OATP1B3 inhibitior + 0.9430 94.30%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9675 96.75%
P-glycoprotein inhibitior - 0.9748 97.48%
P-glycoprotein substrate - 0.9584 95.84%
CYP3A4 substrate - 0.6903 69.03%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8568 85.68%
CYP3A4 inhibition - 0.8699 86.99%
CYP2C9 inhibition - 0.8966 89.66%
CYP2C19 inhibition - 0.9054 90.54%
CYP2D6 inhibition - 0.8818 88.18%
CYP1A2 inhibition - 0.6790 67.90%
CYP2C8 inhibition - 0.9813 98.13%
CYP inhibitory promiscuity - 0.9208 92.08%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8943 89.43%
Carcinogenicity (trinary) Non-required 0.6083 60.83%
Eye corrosion - 0.9777 97.77%
Eye irritation + 0.5499 54.99%
Skin irritation - 0.7650 76.50%
Skin corrosion - 0.9453 94.53%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9160 91.60%
Micronuclear + 0.8900 89.00%
Hepatotoxicity + 0.6929 69.29%
skin sensitisation - 0.9076 90.76%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.6000 60.00%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.4529 45.29%
Acute Oral Toxicity (c) III 0.5854 58.54%
Estrogen receptor binding - 0.8857 88.57%
Androgen receptor binding - 0.8025 80.25%
Thyroid receptor binding - 0.7898 78.98%
Glucocorticoid receptor binding - 0.7729 77.29%
Aromatase binding - 0.7331 73.31%
PPAR gamma - 0.7445 74.45%
Honey bee toxicity - 0.8835 88.35%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.7700 77.00%
Fish aquatic toxicity - 0.5343 53.43%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.07% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.06% 95.56%
CHEMBL2581 P07339 Cathepsin D 87.50% 98.95%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 86.26% 83.10%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.53% 99.23%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.39% 91.11%

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.
There are no matching plants.

Cross-Links

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PubChem 20054975
LOTUS LTS0147023
wikiData Q104917716