5-Aminolevulinic Acid

Details

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Internal ID 08873b56-2bac-4189-a8a9-7ef5daa1499f
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-amino-4-oxopentanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H9NO3/c6-3-4(7)1-2-5(8)9/h1-3,6H2,(H,8,9)
InChI Key ZGXJTSGNIOSYLO-UHFFFAOYSA-N
Popularity 13,921 references in papers

Physical and Chemical Properties

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Molecular Formula C5H9NO3
Molecular Weight 131.13 g/mol
Exact Mass 131.058243149 g/mol
Topological Polar Surface Area (TPSA) 80.40 Ų
XlogP -3.80
Atomic LogP (AlogP) -0.62
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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Aminolevulinic acid
106-60-5
5-Amino-4-oxopentanoic acid
5-Aminolevulinate
delta-aminolevulinic acid
Pentanoic acid, 5-amino-4-oxo-
Aladerm
5-Amino-4-oxovaleric acid
5-ALA
Aminolevulinate
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-Aminolevulinic Acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8066 80.66%
Caco-2 + 0.5817 58.17%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Mitochondria 0.7358 73.58%
OATP2B1 inhibitior - 0.8588 85.88%
OATP1B1 inhibitior + 0.9648 96.48%
OATP1B3 inhibitior + 0.9589 95.89%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9632 96.32%
P-glycoprotein inhibitior - 0.9868 98.68%
P-glycoprotein substrate - 0.9777 97.77%
CYP3A4 substrate - 0.7905 79.05%
CYP2C9 substrate + 0.6183 61.83%
CYP2D6 substrate - 0.7515 75.15%
CYP3A4 inhibition - 0.9187 91.87%
CYP2C9 inhibition - 0.9561 95.61%
CYP2C19 inhibition - 0.9406 94.06%
CYP2D6 inhibition - 0.9608 96.08%
CYP1A2 inhibition - 0.9219 92.19%
CYP2C8 inhibition - 0.9832 98.32%
CYP inhibitory promiscuity - 0.9784 97.84%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7530 75.30%
Carcinogenicity (trinary) Non-required 0.6103 61.03%
Eye corrosion - 0.9520 95.20%
Eye irritation + 0.9018 90.18%
Skin irritation - 0.7668 76.68%
Skin corrosion - 0.6326 63.26%
Ames mutagenesis + 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7336 73.36%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.7625 76.25%
skin sensitisation - 0.9426 94.26%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.8778 87.78%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.7245 72.45%
Acute Oral Toxicity (c) IV 0.6540 65.40%
Estrogen receptor binding - 0.9637 96.37%
Androgen receptor binding - 0.9300 93.00%
Thyroid receptor binding - 0.9083 90.83%
Glucocorticoid receptor binding - 0.8616 86.16%
Aromatase binding - 0.8736 87.36%
PPAR gamma - 0.6952 69.52%
Honey bee toxicity - 0.9604 96.04%
Biodegradation + 0.8750 87.50%
Crustacea aquatic toxicity - 0.9800 98.00%
Fish aquatic toxicity - 0.9489 94.89%

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 92.41% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 88.05% 83.82%
CHEMBL221 P23219 Cyclooxygenase-1 86.58% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.35% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.75% 96.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.77% 91.11%

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 137
LOTUS LTS0149335
wikiData Q238474