(2S)-2-Amino-5-oxopentanoic acid

Details

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Internal ID cf7b19d0-2eb6-4828-aba5-536be879c4b5
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids > L-alpha-amino acids
IUPAC Name (2S)-2-amino-5-oxopentanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H9NO3/c6-4(5(8)9)2-1-3-7/h3-4H,1-2,6H2,(H,8,9)/t4-/m0/s1
InChI Key KABXUUFDPUOJMW-BYPYZUCNSA-N
Popularity 1,225 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 -3.80
Atomic LogP (AlogP) -0.62
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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5-oxo-L-norvaline
gamma-Glutamyl semialdehyde
4-CARBOXY-4-AMINOBUTANAL
L-Norvaline, 5-oxo-
Glutamate gamma-semialdehyde
B517ZPX7HX
L-Glutamic-gamma-semialdehyde
Glutamic acid gamma-semialdehyde
2886-91-1
2-Amino-5-oxopentanoic acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (2S)-2-Amino-5-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 + 0.8870 88.70%
Caco-2 - 0.8477 84.77%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.5264 52.64%
OATP2B1 inhibitior - 0.8453 84.53%
OATP1B1 inhibitior + 0.9624 96.24%
OATP1B3 inhibitior + 0.9549 95.49%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9551 95.51%
P-glycoprotein inhibitior - 0.9920 99.20%
P-glycoprotein substrate - 0.9749 97.49%
CYP3A4 substrate - 0.7551 75.51%
CYP2C9 substrate + 0.5981 59.81%
CYP2D6 substrate - 0.7774 77.74%
CYP3A4 inhibition - 0.9319 93.19%
CYP2C9 inhibition - 0.9755 97.55%
CYP2C19 inhibition - 0.9779 97.79%
CYP2D6 inhibition - 0.9678 96.78%
CYP1A2 inhibition - 0.9376 93.76%
CYP2C8 inhibition - 0.9938 99.38%
CYP inhibitory promiscuity - 0.9955 99.55%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Non-required 0.6959 69.59%
Eye corrosion - 0.9857 98.57%
Eye irritation - 0.7107 71.07%
Skin irritation - 0.8358 83.58%
Skin corrosion + 0.9619 96.19%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8409 84.09%
Micronuclear - 0.5900 59.00%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.9454 94.54%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.7444 74.44%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.7485 74.85%
Acute Oral Toxicity (c) IV 0.6893 68.93%
Estrogen receptor binding - 0.9707 97.07%
Androgen receptor binding - 0.8434 84.34%
Thyroid receptor binding - 0.9050 90.50%
Glucocorticoid receptor binding - 0.8372 83.72%
Aromatase binding - 0.9020 90.20%
PPAR gamma - 0.7988 79.88%
Honey bee toxicity - 0.9403 94.03%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity - 0.9354 93.54%

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 95.21% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.20% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.93% 99.17%
CHEMBL233 P35372 Mu opioid receptor 88.33% 97.93%
CHEMBL221 P23219 Cyclooxygenase-1 87.29% 90.17%
CHEMBL236 P41143 Delta opioid receptor 86.04% 99.35%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 84.91% 92.29%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 84.90% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.68% 95.56%

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 193305
LOTUS LTS0213675
wikiData Q2823261