N-(5-methyl-3-oxohexyl)alanine

Details

Top
Internal ID f851a3cd-230b-4484-bb37-b5f078be47a9
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Alanine and derivatives
IUPAC Name (2S)-2-[(5-methyl-3-oxohexyl)amino]propanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H19NO3/c1-7(2)6-9(12)4-5-11-8(3)10(13)14/h7-8,11H,4-6H2,1-3H3,(H,13,14)/t8-/m0/s1
InChI Key VHHUMCJOXTZJOX-QMMMGPOBSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C10H19NO3
Molecular Weight 201.26 g/mol
Exact Mass 201.13649347 g/mol
Topological Polar Surface Area (TPSA) 66.40 Ų
XlogP -1.60
Atomic LogP (AlogP) 1.05
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

Top
(2S)-2-[(5-methyl-3-oxohexyl)amino]propanoic acid
CHEBI:173550

2D Structure

Top
2D Structure of N-(5-methyl-3-oxohexyl)alanine

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8456 84.56%
Caco-2 + 0.6490 64.90%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.7573 75.73%
OATP2B1 inhibitior - 0.8495 84.95%
OATP1B1 inhibitior + 0.9253 92.53%
OATP1B3 inhibitior + 0.9456 94.56%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9461 94.61%
P-glycoprotein inhibitior - 0.9794 97.94%
P-glycoprotein substrate - 0.8528 85.28%
CYP3A4 substrate - 0.6724 67.24%
CYP2C9 substrate + 0.6153 61.53%
CYP2D6 substrate - 0.7802 78.02%
CYP3A4 inhibition - 0.9320 93.20%
CYP2C9 inhibition - 0.9065 90.65%
CYP2C19 inhibition - 0.9382 93.82%
CYP2D6 inhibition - 0.8798 87.98%
CYP1A2 inhibition - 0.8446 84.46%
CYP2C8 inhibition - 0.9880 98.80%
CYP inhibitory promiscuity - 0.9785 97.85%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.7149 71.49%
Eye corrosion - 0.9314 93.14%
Eye irritation + 0.5929 59.29%
Skin irritation - 0.8076 80.76%
Skin corrosion - 0.9114 91.14%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7181 71.81%
Micronuclear - 0.6900 69.00%
Hepatotoxicity + 0.5052 50.52%
skin sensitisation - 0.8367 83.67%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.9275 92.75%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.4658 46.58%
Acute Oral Toxicity (c) III 0.6773 67.73%
Estrogen receptor binding - 0.9338 93.38%
Androgen receptor binding - 0.8721 87.21%
Thyroid receptor binding - 0.7690 76.90%
Glucocorticoid receptor binding - 0.8831 88.31%
Aromatase binding - 0.8918 89.18%
PPAR gamma - 0.7990 79.90%
Honey bee toxicity - 0.9466 94.66%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.8800 88.00%
Fish aquatic toxicity - 0.6177 61.77%

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
CHEMBL4040 P28482 MAP kinase ERK2 97.31% 83.82%
CHEMBL221 P23219 Cyclooxygenase-1 94.64% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.19% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.57% 98.95%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 90.07% 100.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.76% 85.14%
CHEMBL3308 P55212 Caspase-6 85.37% 97.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.28% 99.17%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 82.09% 96.47%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.27% 96.00%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.03% 94.33%

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.
Cycas circinalis

Cross-Links

Top
PubChem 10631902
LOTUS LTS0177904
wikiData Q105286442