5-Amino-2-oxopentanoic acid

Details

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Internal ID cd05868b-8de5-4ef7-9425-dd01004f5321
Taxonomy Organic acids and derivatives > Keto acids and derivatives > Short-chain keto acids and derivatives
IUPAC Name 5-amino-2-oxopentanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H9NO3/c6-3-1-2-4(7)5(8)9/h1-3,6H2,(H,8,9)
InChI Key BWHGMFYTDQEALD-UHFFFAOYSA-N
Popularity 16 references in papers

Physical and Chemical Properties

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Molecular Formula C5H9NO3
Molecular Weight 131.13 g/mol
Exact Mass 131.058243149 g/mol
Topological Polar Surface Area (TPSA) 80.40 Ų
XlogP -3.30
Atomic LogP (AlogP) -0.62
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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2-Oxo-5-aminovalerate
2-Oxo-5-aminopentanoate
2-Oxo-5-amino-pentanoate
2-oxo-5-amino-pentanoic acid
5-Amino-2-oxopentanoate
alpha-Keto-delta-aminopentanoate
2000-59-1
2-Oxo-5-aminopentanoic acid
5-amino-2-oxovaleric acid
C01110
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 5-Amino-2-oxopentanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8322 83.22%
Caco-2 - 0.6127 61.27%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6137 61.37%
OATP2B1 inhibitior - 0.8460 84.60%
OATP1B1 inhibitior + 0.9605 96.05%
OATP1B3 inhibitior + 0.9550 95.50%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9587 95.87%
P-glycoprotein inhibitior - 0.9857 98.57%
P-glycoprotein substrate - 0.9634 96.34%
CYP3A4 substrate - 0.7819 78.19%
CYP2C9 substrate + 0.6159 61.59%
CYP2D6 substrate - 0.7619 76.19%
CYP3A4 inhibition - 0.9374 93.74%
CYP2C9 inhibition - 0.9525 95.25%
CYP2C19 inhibition - 0.9534 95.34%
CYP2D6 inhibition - 0.9745 97.45%
CYP1A2 inhibition - 0.9393 93.93%
CYP2C8 inhibition - 0.9766 97.66%
CYP inhibitory promiscuity - 0.9865 98.65%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7046 70.46%
Carcinogenicity (trinary) Non-required 0.6913 69.13%
Eye corrosion - 0.9231 92.31%
Eye irritation + 0.7823 78.23%
Skin irritation - 0.6847 68.47%
Skin corrosion + 0.7002 70.02%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7676 76.76%
Micronuclear - 0.8368 83.68%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation - 0.9112 91.12%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity - 0.8778 87.78%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.6711 67.11%
Acute Oral Toxicity (c) IV 0.6460 64.60%
Estrogen receptor binding - 0.9535 95.35%
Androgen receptor binding - 0.8807 88.07%
Thyroid receptor binding - 0.8594 85.94%
Glucocorticoid receptor binding - 0.8367 83.67%
Aromatase binding - 0.8397 83.97%
PPAR gamma - 0.7318 73.18%
Honey bee toxicity - 0.9849 98.49%
Biodegradation + 0.8750 87.50%
Crustacea aquatic toxicity - 0.8400 84.00%
Fish aquatic toxicity - 0.9851 98.51%

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 91.22% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.72% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.46% 96.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.45% 91.11%
CHEMBL4581 P52732 Kinesin-like protein 1 81.66% 93.18%

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 439402
LOTUS LTS0001342
wikiData Q27121579