Butanoic acid, 3-amino-4-oxo-, (3S)-

Details

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Internal ID 6612f9c6-3c19-406b-9b73-0219014e2c4a
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Amino acids and derivatives > Beta amino acids and derivatives
IUPAC Name (3S)-3-amino-4-oxobutanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C4H7NO3/c5-3(2-6)1-4(7)8/h2-3H,1,5H2,(H,7,8)/t3-/m0/s1
InChI Key CGJJPOYORMGCGE-VKHMYHEASA-N
Popularity 1,266 references in papers

Physical and Chemical Properties

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Molecular Formula C4H7NO3
Molecular Weight 117.10 g/mol
Exact Mass 117.042593085 g/mol
Topological Polar Surface Area (TPSA) 80.40 Ų
XlogP -3.90
Atomic LogP (AlogP) -1.01
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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72R2D95DRX
UNII-72R2D95DRX
Succinaldehydic acid, 3-amino-, L-
Butanoic acid, 3-amino-4-oxo-, (S)-
Butanoic acid, 3-amino-4-oxo-, (3S)-
21653-98-5
RefChem:200003
aspartic aldehyde
SCHEMBL8535
SCHEMBL8536
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Butanoic acid, 3-amino-4-oxo-, (3S)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9300 93.00%
Caco-2 - 0.6462 64.62%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Lysosomes 0.4533 45.33%
OATP2B1 inhibitior - 0.8631 86.31%
OATP1B1 inhibitior + 0.9637 96.37%
OATP1B3 inhibitior + 0.9456 94.56%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9520 95.20%
P-glycoprotein inhibitior - 0.9851 98.51%
P-glycoprotein substrate - 0.9802 98.02%
CYP3A4 substrate - 0.7945 79.45%
CYP2C9 substrate + 0.6147 61.47%
CYP2D6 substrate - 0.7660 76.60%
CYP3A4 inhibition - 0.9582 95.82%
CYP2C9 inhibition - 0.9695 96.95%
CYP2C19 inhibition - 0.9737 97.37%
CYP2D6 inhibition - 0.9611 96.11%
CYP1A2 inhibition - 0.9719 97.19%
CYP2C8 inhibition - 0.9744 97.44%
CYP inhibitory promiscuity - 0.9947 99.47%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7200 72.00%
Carcinogenicity (trinary) Non-required 0.7108 71.08%
Eye corrosion - 0.9489 94.89%
Eye irritation + 0.8383 83.83%
Skin irritation - 0.7680 76.80%
Skin corrosion - 0.8700 87.00%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8603 86.03%
Micronuclear - 0.5026 50.26%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.9498 94.98%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.7333 73.33%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity - 0.6361 63.61%
Acute Oral Toxicity (c) III 0.5450 54.50%
Estrogen receptor binding - 0.9229 92.29%
Androgen receptor binding - 0.8845 88.45%
Thyroid receptor binding - 0.9125 91.25%
Glucocorticoid receptor binding - 0.8922 89.22%
Aromatase binding - 0.8635 86.35%
PPAR gamma - 0.8067 80.67%
Honey bee toxicity - 0.9398 93.98%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.9200 92.00%
Fish aquatic toxicity - 0.9536 95.36%

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 92.67% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 89.83% 83.82%
CHEMBL2581 P07339 Cathepsin D 85.03% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.83% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 84.49% 90.17%

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.
Ageratum conyzoides
Changium smyrnioides
Cistanche deserticola
Ficus simplicissima
Polygonatum sibiricum

Cross-Links

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PubChem 6540254
NPASS NPC57429