L-Aspartate 4-semialdehyde

Details

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Internal ID baf9bd83-4e95-4061-aa89-6789fdf03de6
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids
IUPAC Name (2S)-2-amino-4-oxobutanoate
SMILES (Canonical) C(C=O)C(C(=O)[O-])N
SMILES (Isomeric) C(C=O)[C@@H](C(=O)[O-])N
InChI InChI=1S/C4H7NO3/c5-3(1-2-6)4(7)8/h2-3H,1,5H2,(H,7,8)/p-1/t3-/m0/s1
InChI Key HOSWPDPVFBCLSY-VKHMYHEASA-M
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C4H6NO3-
Molecular Weight 116.10 g/mol
Exact Mass 116.034768053 g/mol
Topological Polar Surface Area (TPSA) 83.20 Ų
XlogP -3.30
Atomic LogP (AlogP) -2.35
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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Aspartate beta-semialdehyde
(2S)-2-amino-4-oxobutanoate
CHEBI:13086
Q27108965

2D Structure

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2D Structure of L-Aspartate 4-semialdehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9689 96.89%
Caco-2 - 0.9160 91.60%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Lysosomes 0.5458 54.58%
OATP2B1 inhibitior - 0.8559 85.59%
OATP1B1 inhibitior + 0.9406 94.06%
OATP1B3 inhibitior + 0.9510 95.10%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9390 93.90%
P-glycoprotein inhibitior - 0.9833 98.33%
P-glycoprotein substrate - 0.9760 97.60%
CYP3A4 substrate - 0.7526 75.26%
CYP2C9 substrate + 0.5991 59.91%
CYP2D6 substrate - 0.8159 81.59%
CYP3A4 inhibition - 0.9649 96.49%
CYP2C9 inhibition - 0.9646 96.46%
CYP2C19 inhibition - 0.9543 95.43%
CYP2D6 inhibition - 0.9456 94.56%
CYP1A2 inhibition - 0.9115 91.15%
CYP2C8 inhibition - 0.9824 98.24%
CYP inhibitory promiscuity - 0.9893 98.93%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6400 64.00%
Carcinogenicity (trinary) Non-required 0.6574 65.74%
Eye corrosion - 0.6855 68.55%
Eye irritation + 0.6610 66.10%
Skin irritation - 0.6153 61.53%
Skin corrosion - 0.5882 58.82%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8921 89.21%
Micronuclear - 0.5026 50.26%
Hepatotoxicity + 0.6750 67.50%
skin sensitisation - 0.9456 94.56%
Respiratory toxicity - 0.7111 71.11%
Reproductive toxicity - 0.6111 61.11%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.7568 75.68%
Acute Oral Toxicity (c) III 0.6097 60.97%
Estrogen receptor binding - 0.9521 95.21%
Androgen receptor binding - 0.8529 85.29%
Thyroid receptor binding - 0.9216 92.16%
Glucocorticoid receptor binding - 0.8634 86.34%
Aromatase binding - 0.9072 90.72%
PPAR gamma - 0.8133 81.33%
Honey bee toxicity - 0.9047 90.47%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity - 0.8900 89.00%
Fish aquatic toxicity - 0.9218 92.18%

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 99.72% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.92% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.04% 95.56%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 82.81% 92.29%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.81% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.86% 96.95%

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 5461143
LOTUS LTS0097459
wikiData Q27108965