(2R)-4-amino-2-azaniumyl-4-oxobutanoate

Details

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Internal ID a490d6ca-e20e-4669-9178-f424e8a7a58f
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Asparagine and derivatives
IUPAC Name (2R)-4-amino-2-azaniumyl-4-oxobutanoate
SMILES (Canonical) C(C(C(=O)[O-])[NH3+])C(=O)N
SMILES (Isomeric) C([C@H](C(=O)[O-])[NH3+])C(=O)N
InChI InChI=1S/C4H8N2O3/c5-2(4(8)9)1-3(6)7/h2H,1,5H2,(H2,6,7)(H,8,9)/t2-/m1/s1
InChI Key DCXYFEDJOCDNAF-UWTATZPHSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C4H8N2O3
Molecular Weight 132.12 g/mol
Exact Mass 132.05349212 g/mol
Topological Polar Surface Area (TPSA) 111.00 Ų
XlogP -2.80
Atomic LogP (AlogP) -3.78
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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CHEBI:74337
(2R)-4-amino-2-azaniumyl-4-oxobutanoate

2D Structure

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2D Structure of (2R)-4-amino-2-azaniumyl-4-oxobutanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7055 70.55%
Caco-2 - 0.9636 96.36%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.5819 58.19%
OATP2B1 inhibitior - 0.8597 85.97%
OATP1B1 inhibitior + 0.9694 96.94%
OATP1B3 inhibitior + 0.9477 94.77%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9552 95.52%
P-glycoprotein inhibitior - 0.9875 98.75%
P-glycoprotein substrate - 0.9480 94.80%
CYP3A4 substrate - 0.7225 72.25%
CYP2C9 substrate - 0.8052 80.52%
CYP2D6 substrate - 0.8340 83.40%
CYP3A4 inhibition - 0.9552 95.52%
CYP2C9 inhibition - 0.9510 95.10%
CYP2C19 inhibition - 0.9454 94.54%
CYP2D6 inhibition - 0.9585 95.85%
CYP1A2 inhibition - 0.9228 92.28%
CYP2C8 inhibition - 0.9907 99.07%
CYP inhibitory promiscuity - 0.9704 97.04%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7300 73.00%
Carcinogenicity (trinary) Non-required 0.6965 69.65%
Eye corrosion - 0.9521 95.21%
Eye irritation + 0.6556 65.56%
Skin irritation - 0.7977 79.77%
Skin corrosion - 0.9664 96.64%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8698 86.98%
Micronuclear + 0.6200 62.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.9518 95.18%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.5547 55.47%
Acute Oral Toxicity (c) III 0.5500 55.00%
Estrogen receptor binding - 0.9512 95.12%
Androgen receptor binding - 0.8516 85.16%
Thyroid receptor binding - 0.9148 91.48%
Glucocorticoid receptor binding - 0.8129 81.29%
Aromatase binding - 0.9093 90.93%
PPAR gamma - 0.6788 67.88%
Honey bee toxicity - 0.8915 89.15%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.8700 87.00%
Fish aquatic toxicity - 0.9335 93.35%

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 98.54% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.64% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 88.78% 96.95%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 80.84% 100.00%

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.
Asparagus cochinchinensis
Asparagus officinalis
Scrophularia ningpoensis

Cross-Links

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PubChem 6991971
NPASS NPC153370