(2S,3R)-3-hydroxy-2-(methylamino)pentanoic acid

Details

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Internal ID 4331e21d-b4f2-4b03-abdc-d65bb3e3b45e
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alpha amino acids > L-alpha-amino acids
IUPAC Name (2S,3R)-3-hydroxy-2-(methylamino)pentanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H13NO3/c1-3-4(8)5(7-2)6(9)10/h4-5,7-8H,3H2,1-2H3,(H,9,10)/t4-,5+/m1/s1
InChI Key HNCSHNXJJWIGTP-UHNVWZDZSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C6H13NO3
Molecular Weight 147.17 g/mol
Exact Mass 147.08954328 g/mol
Topological Polar Surface Area (TPSA) 69.60 Ų
XlogP -2.60
Atomic LogP (AlogP) -0.57
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2S,3R)-3-hydroxy-2-(methylamino)pentanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8539 85.39%
Caco-2 - 0.5188 51.88%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.5715 57.15%
OATP2B1 inhibitior - 0.8356 83.56%
OATP1B1 inhibitior + 0.9200 92.00%
OATP1B3 inhibitior + 0.9345 93.45%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9564 95.64%
P-glycoprotein inhibitior - 0.9762 97.62%
P-glycoprotein substrate - 0.9545 95.45%
CYP3A4 substrate - 0.7439 74.39%
CYP2C9 substrate - 0.8000 80.00%
CYP2D6 substrate - 0.7148 71.48%
CYP3A4 inhibition - 0.9417 94.17%
CYP2C9 inhibition - 0.9129 91.29%
CYP2C19 inhibition - 0.9243 92.43%
CYP2D6 inhibition - 0.8765 87.65%
CYP1A2 inhibition - 0.8534 85.34%
CYP2C8 inhibition - 0.9876 98.76%
CYP inhibitory promiscuity - 0.9499 94.99%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7900 79.00%
Carcinogenicity (trinary) Non-required 0.6719 67.19%
Eye corrosion - 0.9740 97.40%
Eye irritation + 0.5808 58.08%
Skin irritation - 0.7878 78.78%
Skin corrosion - 0.8407 84.07%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6880 68.80%
Micronuclear - 0.5026 50.26%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.9266 92.66%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.6788 67.88%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.7127 71.27%
Acute Oral Toxicity (c) III 0.7070 70.70%
Estrogen receptor binding - 0.9103 91.03%
Androgen receptor binding - 0.8968 89.68%
Thyroid receptor binding - 0.8809 88.09%
Glucocorticoid receptor binding - 0.9076 90.76%
Aromatase binding - 0.8985 89.85%
PPAR gamma - 0.8135 81.35%
Honey bee toxicity - 0.9664 96.64%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.9200 92.00%
Fish aquatic toxicity - 0.9392 93.92%

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 95.09% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.67% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.63% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 88.35% 90.17%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 84.05% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.01% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.03% 96.95%

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.
Crotalaria juncea

Cross-Links

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PubChem 55286555
LOTUS LTS0106785
wikiData Q105030808