(2S,3S)-2-azaniumyl-3-carbamoyl-3-hydroxypropanoate

Details

Top
Internal ID 79140524-796c-41a9-8e22-365face074cd
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Asparagine and derivatives
IUPAC Name (2S,3S)-4-amino-2-azaniumyl-3-hydroxy-4-oxobutanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C4H8N2O4/c5-1(4(9)10)2(7)3(6)8/h1-2,7H,5H2,(H2,6,8)(H,9,10)/t1-,2-/m0/s1
InChI Key VQTLPSCRBFYDNX-LWMBPPNESA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C4H8N2O4
Molecular Weight 148.12 g/mol
Exact Mass 148.04840674 g/mol
Topological Polar Surface Area (TPSA) 131.00 Ų
XlogP -4.40
Atomic LogP (AlogP) -4.81
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

Top
(3S)-3-hydroxy-L-asparagine zwitterion
(2S,3S)-2-azaniumyl-3-carbamoyl-3-hydroxypropanoate
(2S,3S)-4-amino-2-ammonio-3-hydroxy-4-oxobutanoate
(2S,3S)-4-amino-2-azaniumyl-3-hydroxy-4-oxobutanoate

2D Structure

Top
2D Structure of (2S,3S)-2-azaniumyl-3-carbamoyl-3-hydroxypropanoate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.8368 83.68%
Caco-2 - 0.9758 97.58%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.5964 59.64%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9670 96.70%
OATP1B3 inhibitior + 0.9475 94.75%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9739 97.39%
P-glycoprotein inhibitior - 0.9832 98.32%
P-glycoprotein substrate - 0.9521 95.21%
CYP3A4 substrate - 0.7357 73.57%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8367 83.67%
CYP3A4 inhibition - 0.8161 81.61%
CYP2C9 inhibition - 0.9363 93.63%
CYP2C19 inhibition - 0.9327 93.27%
CYP2D6 inhibition - 0.9395 93.95%
CYP1A2 inhibition - 0.9019 90.19%
CYP2C8 inhibition - 0.9883 98.83%
CYP inhibitory promiscuity - 0.9930 99.30%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7476 74.76%
Carcinogenicity (trinary) Non-required 0.6962 69.62%
Eye corrosion - 0.9927 99.27%
Eye irritation + 0.7082 70.82%
Skin irritation - 0.6990 69.90%
Skin corrosion - 0.9865 98.65%
Ames mutagenesis - 0.6454 64.54%
Human Ether-a-go-go-Related Gene inhibition - 0.8776 87.76%
Micronuclear + 0.8100 81.00%
Hepatotoxicity + 0.7175 71.75%
skin sensitisation - 0.9435 94.35%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.6118 61.18%
Acute Oral Toxicity (c) III 0.5598 55.98%
Estrogen receptor binding - 0.9011 90.11%
Androgen receptor binding - 0.8841 88.41%
Thyroid receptor binding - 0.7759 77.59%
Glucocorticoid receptor binding - 0.7425 74.25%
Aromatase binding - 0.8858 88.58%
PPAR gamma - 0.5971 59.71%
Honey bee toxicity - 0.8455 84.55%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.8400 84.00%
Fish aquatic toxicity - 0.9056 90.56%

Targets

Top

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 92.19% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.21% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.77% 97.21%

Plants that contains it

Top
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.
Ophiopogon japonicus

Cross-Links

Top
PubChem 46878457
NPASS NPC283312