5-Aminovaleric acid

Details

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Internal ID ede632c0-9472-41f0-9d38-d91f74ff0953
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Amino acids and derivatives > Delta amino acids and derivatives
IUPAC Name 5-aminopentanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H11NO2/c6-4-2-1-3-5(7)8/h1-4,6H2,(H,7,8)
InChI Key JJMDCOVWQOJGCB-UHFFFAOYSA-N
Popularity 590 references in papers

Physical and Chemical Properties

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Molecular Formula C5H11NO2
Molecular Weight 117.15 g/mol
Exact Mass 117.078978594 g/mol
Topological Polar Surface Area (TPSA) 63.30 Ų
XlogP -2.60
Atomic LogP (AlogP) 0.20
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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5-Aminopentanoic acid
660-88-8
Homopiperidinic acid
Pentanoic acid, 5-amino-
H-5-Ava-OH
5-amino-pentanoic acid
Valeric acid, 5-amino-
delta-Amino-n-valeric acid
delta-Aminovaleric acid
5-aminopentanoate
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 5-Aminovaleric acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9600 96.00%
Caco-2 + 0.6556 65.56%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.5222 52.22%
OATP2B1 inhibitior - 0.8521 85.21%
OATP1B1 inhibitior + 0.9621 96.21%
OATP1B3 inhibitior + 0.9506 95.06%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9392 93.92%
P-glycoprotein inhibitior - 0.9862 98.62%
P-glycoprotein substrate - 0.9750 97.50%
CYP3A4 substrate - 0.8004 80.04%
CYP2C9 substrate + 0.6180 61.80%
CYP2D6 substrate - 0.7526 75.26%
CYP3A4 inhibition - 0.9432 94.32%
CYP2C9 inhibition - 0.9604 96.04%
CYP2C19 inhibition - 0.9767 97.67%
CYP2D6 inhibition - 0.9760 97.60%
CYP1A2 inhibition - 0.9254 92.54%
CYP2C8 inhibition - 0.9872 98.72%
CYP inhibitory promiscuity - 0.9764 97.64%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6235 62.35%
Carcinogenicity (trinary) Non-required 0.5880 58.80%
Eye corrosion - 0.9506 95.06%
Eye irritation + 0.8927 89.27%
Skin irritation - 0.6259 62.59%
Skin corrosion + 0.6415 64.15%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7833 78.33%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.9125 91.25%
skin sensitisation - 0.9090 90.90%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity - 0.9444 94.44%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.6810 68.10%
Acute Oral Toxicity (c) IV 0.5205 52.05%
Estrogen receptor binding - 0.9547 95.47%
Androgen receptor binding - 0.9211 92.11%
Thyroid receptor binding - 0.9079 90.79%
Glucocorticoid receptor binding - 0.8631 86.31%
Aromatase binding - 0.8351 83.51%
PPAR gamma - 0.7651 76.51%
Honey bee toxicity - 0.9855 98.55%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity - 0.9620 96.20%

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 94.88% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.11% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.53% 91.11%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 85.88% 92.26%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.57% 96.95%
CHEMBL4581 P52732 Kinesin-like protein 1 83.60% 93.18%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.28% 97.21%
CHEMBL1255126 O15151 Protein Mdm4 80.47% 90.20%

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 138
LOTUS LTS0241502
wikiData Q11751639