2-Ammonio-3-methylpentanoate

Details

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Internal ID 5d4aa4bd-519e-4517-bca8-696b438816ce
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives > Isoleucine and derivatives
IUPAC Name 2-azaniumyl-3-methylpentanoate
SMILES (Canonical) CCC(C)C(C(=O)[O-])[NH3+]
SMILES (Isomeric) CCC(C)C(C(=O)[O-])[NH3+]
InChI InChI=1S/C6H13NO2/c1-3-4(2)5(7)6(8)9/h4-5H,3,7H2,1-2H3,(H,8,9)
InChI Key AGPKZVBTJJNPAG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C6H13NO2
Molecular Weight 131.17 g/mol
Exact Mass 131.094628657 g/mol
Topological Polar Surface Area (TPSA) 67.80 Ų
XlogP -1.10
Atomic LogP (AlogP) -1.61
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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STL451523

2D Structure

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2D Structure of 2-Ammonio-3-methylpentanoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9883 98.83%
Caco-2 - 0.7801 78.01%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Lysosomes 0.4299 42.99%
OATP2B1 inhibitior - 0.8407 84.07%
OATP1B1 inhibitior + 0.9208 92.08%
OATP1B3 inhibitior + 0.9427 94.27%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9245 92.45%
P-glycoprotein inhibitior - 0.9837 98.37%
P-glycoprotein substrate - 0.9293 92.93%
CYP3A4 substrate - 0.7358 73.58%
CYP2C9 substrate + 0.6211 62.11%
CYP2D6 substrate - 0.8433 84.33%
CYP3A4 inhibition - 0.9646 96.46%
CYP2C9 inhibition - 0.9122 91.22%
CYP2C19 inhibition - 0.9433 94.33%
CYP2D6 inhibition - 0.8379 83.79%
CYP1A2 inhibition - 0.8099 80.99%
CYP2C8 inhibition - 0.9896 98.96%
CYP inhibitory promiscuity - 0.9427 94.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5426 54.26%
Carcinogenicity (trinary) Non-required 0.5811 58.11%
Eye corrosion + 0.5196 51.96%
Eye irritation - 0.6102 61.02%
Skin irritation + 0.5168 51.68%
Skin corrosion + 0.6701 67.01%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8144 81.44%
Micronuclear + 0.5600 56.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.9113 91.13%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.5444 54.44%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity - 0.5592 55.92%
Acute Oral Toxicity (c) III 0.7530 75.30%
Estrogen receptor binding - 0.9106 91.06%
Androgen receptor binding - 0.8742 87.42%
Thyroid receptor binding - 0.8803 88.03%
Glucocorticoid receptor binding - 0.9154 91.54%
Aromatase binding - 0.8515 85.15%
PPAR gamma - 0.8586 85.86%
Honey bee toxicity - 0.9629 96.29%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.8600 86.00%
Fish aquatic toxicity - 0.4881 48.81%

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 95.61% 96.09%
CHEMBL2581 P07339 Cathepsin D 91.40% 98.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 90.67% 96.95%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 86.12% 97.21%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 85.81% 100.00%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 81.72% 92.86%

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.
Allium sativum
Brassica juncea
Ginkgo biloba
Pogostemon cablin
Sinapis alba
Tussilago farfara

Cross-Links

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PubChem 57397079
NPASS NPC226027