3-Amino-2r-hydroxy-3-methylbutanoic acid

Details

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Internal ID 1410b662-a0f8-475d-9faf-640a3a994289
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 (2R)-3-amino-2-hydroxy-3-methylbutanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H11NO3/c1-5(2,6)3(7)4(8)9/h3,7H,6H2,1-2H3,(H,8,9)/t3-/m0/s1
InChI Key YNEGEPKXRPUBDF-VKHMYHEASA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C5H11NO3
Molecular Weight 133.15 g/mol
Exact Mass 133.07389321 g/mol
Topological Polar Surface Area (TPSA) 83.60 Ų
XlogP -3.40
Atomic LogP (AlogP) -0.83
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Amino-2r-hydroxy-3-methylbutanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9171 91.71%
Caco-2 - 0.8894 88.94%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.4782 47.82%
OATP2B1 inhibitior - 0.8585 85.85%
OATP1B1 inhibitior + 0.9770 97.70%
OATP1B3 inhibitior + 0.9497 94.97%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9457 94.57%
P-glycoprotein inhibitior - 0.9825 98.25%
P-glycoprotein substrate - 0.9833 98.33%
CYP3A4 substrate - 0.7535 75.35%
CYP2C9 substrate + 0.5906 59.06%
CYP2D6 substrate - 0.7795 77.95%
CYP3A4 inhibition - 0.9311 93.11%
CYP2C9 inhibition - 0.8573 85.73%
CYP2C19 inhibition - 0.9145 91.45%
CYP2D6 inhibition - 0.9467 94.67%
CYP1A2 inhibition - 0.7327 73.27%
CYP2C8 inhibition - 0.9939 99.39%
CYP inhibitory promiscuity - 0.9700 97.00%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6223 62.23%
Carcinogenicity (trinary) Non-required 0.6926 69.26%
Eye corrosion - 0.9846 98.46%
Eye irritation + 0.7601 76.01%
Skin irritation - 0.6862 68.62%
Skin corrosion - 0.9017 90.17%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8295 82.95%
Micronuclear + 0.5500 55.00%
Hepatotoxicity + 0.7250 72.50%
skin sensitisation - 0.9059 90.59%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.7047 70.47%
Acute Oral Toxicity (c) III 0.7638 76.38%
Estrogen receptor binding - 0.9005 90.05%
Androgen receptor binding - 0.8976 89.76%
Thyroid receptor binding - 0.8310 83.10%
Glucocorticoid receptor binding - 0.8275 82.75%
Aromatase binding - 0.8977 89.77%
PPAR gamma - 0.8226 82.26%
Honey bee toxicity - 0.9366 93.66%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.9200 92.00%
Fish aquatic toxicity - 0.8907 89.07%

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 93.51% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 90.38% 83.82%
CHEMBL2581 P07339 Cathepsin D 88.55% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.26% 97.29%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 85.44% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.00% 93.56%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 80.43% 92.29%

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 15198454
LOTUS LTS0006181
wikiData Q105350902