2-Amino-5-oxohexanoic acid

Details

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Internal ID 6cffaa64-4c01-4547-97ef-a13915341ca0
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-5-oxohexanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H11NO3/c1-4(8)2-3-5(7)6(9)10/h5H,2-3,7H2,1H3,(H,9,10)
InChI Key KSIJECNNZVKMJG-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C6H11NO3
Molecular Weight 145.16 g/mol
Exact Mass 145.07389321 g/mol
Topological Polar Surface Area (TPSA) 80.40 Ų
XlogP -3.50
Atomic LogP (AlogP) -0.23
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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2-Amino-5-oxohexanoate
24438-52-6
2-amino-5-oxohexanoicacid
SCHEMBL1330943
CHEBI:19450
AKOS019285077
PD040659
C05825
EN300-109867

2D Structure

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2D Structure of 2-Amino-5-oxohexanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9425 94.25%
Caco-2 - 0.9315 93.15%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.5336 53.36%
OATP2B1 inhibitior - 0.8445 84.45%
OATP1B1 inhibitior + 0.9683 96.83%
OATP1B3 inhibitior + 0.9539 95.39%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9552 95.52%
P-glycoprotein inhibitior - 0.9908 99.08%
P-glycoprotein substrate - 0.9710 97.10%
CYP3A4 substrate - 0.7645 76.45%
CYP2C9 substrate - 0.5905 59.05%
CYP2D6 substrate - 0.7960 79.60%
CYP3A4 inhibition - 0.9549 95.49%
CYP2C9 inhibition - 0.9611 96.11%
CYP2C19 inhibition - 0.9485 94.85%
CYP2D6 inhibition - 0.9378 93.78%
CYP1A2 inhibition - 0.7427 74.27%
CYP2C8 inhibition - 0.9950 99.50%
CYP inhibitory promiscuity - 0.9871 98.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7811 78.11%
Carcinogenicity (trinary) Non-required 0.7396 73.96%
Eye corrosion - 0.9719 97.19%
Eye irritation - 0.7624 76.24%
Skin irritation - 0.7728 77.28%
Skin corrosion + 0.8189 81.89%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8531 85.31%
Micronuclear - 0.6200 62.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.9274 92.74%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.6865 68.65%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.7745 77.45%
Acute Oral Toxicity (c) III 0.6229 62.29%
Estrogen receptor binding - 0.9558 95.58%
Androgen receptor binding - 0.8950 89.50%
Thyroid receptor binding - 0.9324 93.24%
Glucocorticoid receptor binding - 0.8631 86.31%
Aromatase binding - 0.9292 92.92%
PPAR gamma - 0.9259 92.59%
Honey bee toxicity - 0.9743 97.43%
Biodegradation + 0.8750 87.50%
Crustacea aquatic toxicity - 0.9000 90.00%
Fish aquatic toxicity - 0.8246 82.46%

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 98.76% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.63% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.55% 99.17%
CHEMBL2581 P07339 Cathepsin D 88.51% 98.95%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 88.41% 92.29%
CHEMBL236 P41143 Delta opioid receptor 83.48% 99.35%
CHEMBL221 P23219 Cyclooxygenase-1 82.63% 90.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.50% 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.
There are no matching plants.

Cross-Links

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PubChem 440805
LOTUS LTS0017728
wikiData Q105145425