2-Amino-3-(hydroxycarbamoylamino)propanoic acid

Details

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Internal ID 5ef1527a-56b9-41f8-b4c7-3967f3ee780b
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids
IUPAC Name 2-amino-3-(hydroxycarbamoylamino)propanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C4H9N3O4/c5-2(3(8)9)1-6-4(10)7-11/h2,11H,1,5H2,(H,8,9)(H2,6,7,10)
InChI Key XAFCEWGVBTWSTN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C4H9N3O4
Molecular Weight 163.13 g/mol
Exact Mass 163.05930578 g/mol
Topological Polar Surface Area (TPSA) 125.00 Ų
XlogP -4.70
Atomic LogP (AlogP) -1.91
H-Bond Acceptor 4
H-Bond Donor 5
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Amino-3-(hydroxycarbamoylamino)propanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5570 55.70%
Caco-2 - 0.9750 97.50%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.5206 52.06%
OATP2B1 inhibitior - 0.8516 85.16%
OATP1B1 inhibitior + 0.9736 97.36%
OATP1B3 inhibitior + 0.9384 93.84%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9750 97.50%
P-glycoprotein inhibitior - 0.9909 99.09%
P-glycoprotein substrate - 0.9579 95.79%
CYP3A4 substrate - 0.7661 76.61%
CYP2C9 substrate - 0.6124 61.24%
CYP2D6 substrate - 0.8014 80.14%
CYP3A4 inhibition - 0.9114 91.14%
CYP2C9 inhibition - 0.8942 89.42%
CYP2C19 inhibition - 0.8793 87.93%
CYP2D6 inhibition - 0.9291 92.91%
CYP1A2 inhibition - 0.9058 90.58%
CYP2C8 inhibition - 0.9735 97.35%
CYP inhibitory promiscuity - 0.9932 99.32%
UGT catelyzed + 0.5362 53.62%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.6051 60.51%
Eye corrosion - 0.9808 98.08%
Eye irritation - 0.9531 95.31%
Skin irritation - 0.7466 74.66%
Skin corrosion - 0.9425 94.25%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8786 87.86%
Micronuclear + 0.8700 87.00%
Hepatotoxicity + 0.5650 56.50%
skin sensitisation - 0.8402 84.02%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.8171 81.71%
Acute Oral Toxicity (c) III 0.5663 56.63%
Estrogen receptor binding - 0.9354 93.54%
Androgen receptor binding - 0.7547 75.47%
Thyroid receptor binding - 0.8268 82.68%
Glucocorticoid receptor binding - 0.7954 79.54%
Aromatase binding - 0.9327 93.27%
PPAR gamma - 0.9436 94.36%
Honey bee toxicity - 0.9601 96.01%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.9300 93.00%
Fish aquatic toxicity - 0.8499 84.99%

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 97.75% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.01% 96.09%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 94.90% 92.29%
CHEMBL221 P23219 Cyclooxygenase-1 93.41% 90.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 91.53% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 90.01% 97.21%
CHEMBL2581 P07339 Cathepsin D 83.03% 98.95%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 82.93% 95.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.82% 99.17%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 82.49% 89.67%
CHEMBL1795117 Q8TEK3 Histone-lysine N-methyltransferase, H3 lysine-79 specific 82.44% 93.56%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 81.86% 100.00%

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 23348744
LOTUS LTS0135600
wikiData Q104200795