2-Amino-4-oxo-4-phosphonooxybutanoic acid

Details

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Internal ID 3cfb3d89-23a7-4261-8d16-9614c3bf049b
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Aspartic acid and derivatives
IUPAC Name 2-amino-4-oxo-4-phosphonooxybutanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C4H8NO7P/c5-2(4(7)8)1-3(6)12-13(9,10)11/h2H,1,5H2,(H,7,8)(H2,9,10,11)
InChI Key IXZNKTPIYKDIGG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C4H8NO7P
Molecular Weight 213.08 g/mol
Exact Mass 213.00383859 g/mol
Topological Polar Surface Area (TPSA) 147.00 Ų
XlogP -5.20
Atomic LogP (AlogP) -1.58
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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2-amino-4-oxo-4-phosphonooxybutanoic acid

2D Structure

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2D Structure of 2-Amino-4-oxo-4-phosphonooxybutanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.8346 83.46%
Caco-2 - 0.9527 95.27%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.6064 60.64%
OATP2B1 inhibitior - 0.8574 85.74%
OATP1B1 inhibitior + 0.9696 96.96%
OATP1B3 inhibitior + 0.9386 93.86%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9579 95.79%
P-glycoprotein inhibitior - 0.9756 97.56%
P-glycoprotein substrate - 0.9745 97.45%
CYP3A4 substrate - 0.6860 68.60%
CYP2C9 substrate + 0.5986 59.86%
CYP2D6 substrate - 0.7902 79.02%
CYP3A4 inhibition - 0.8587 85.87%
CYP2C9 inhibition - 0.9294 92.94%
CYP2C19 inhibition - 0.9016 90.16%
CYP2D6 inhibition - 0.9084 90.84%
CYP1A2 inhibition - 0.8335 83.35%
CYP2C8 inhibition - 0.9607 96.07%
CYP inhibitory promiscuity - 0.9939 99.39%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7521 75.21%
Carcinogenicity (trinary) Non-required 0.5679 56.79%
Eye corrosion - 0.7569 75.69%
Eye irritation - 0.8382 83.82%
Skin irritation - 0.8000 80.00%
Skin corrosion - 0.7957 79.57%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7813 78.13%
Micronuclear + 0.7500 75.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.8850 88.50%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.5706 57.06%
Acute Oral Toxicity (c) III 0.5728 57.28%
Estrogen receptor binding - 0.9128 91.28%
Androgen receptor binding - 0.7629 76.29%
Thyroid receptor binding - 0.7528 75.28%
Glucocorticoid receptor binding - 0.7735 77.35%
Aromatase binding - 0.8853 88.53%
PPAR gamma - 0.5851 58.51%
Honey bee toxicity - 0.7052 70.52%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity - 0.6661 66.61%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.64% 96.09%
CHEMBL3230 O95977 Sphingosine 1-phosphate receptor Edg-6 89.54% 94.01%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.70% 96.95%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 87.76% 95.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 87.42% 97.29%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.71% 94.45%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 85.03% 97.21%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.01% 99.17%

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 832
LOTUS LTS0076895
wikiData Q105122597