Levulinic Acid

Details

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Internal ID 8270617e-1711-4b38-8ad1-e9a5e6fdd430
Taxonomy Organic acids and derivatives > Keto acids and derivatives > Gamma-keto acids and derivatives
IUPAC Name 4-oxopentanoic acid
SMILES (Canonical) CC(=O)CCC(=O)O
SMILES (Isomeric) CC(=O)CCC(=O)O
InChI InChI=1S/C5H8O3/c1-4(6)2-3-5(7)8/h2-3H2,1H3,(H,7,8)
InChI Key JOOXCMJARBKPKM-UHFFFAOYSA-N
Popularity 3,265 references in papers

Physical and Chemical Properties

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Molecular Formula C5H8O3
Molecular Weight 116.11 g/mol
Exact Mass 116.047344113 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP -0.50
Atomic LogP (AlogP) 0.44
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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4-Oxopentanoic acid
123-76-2
Laevulinic acid
4-Oxovaleric acid
Pentanoic acid, 4-oxo-
Levulic acid
3-Acetylpropionic acid
4-Ketovaleric acid
LEVA
gamma-Ketovaleric acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Levulinic Acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9791 97.91%
Caco-2 + 0.6871 68.71%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.8475 84.75%
OATP2B1 inhibitior - 0.8450 84.50%
OATP1B1 inhibitior + 0.9431 94.31%
OATP1B3 inhibitior + 0.9528 95.28%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9571 95.71%
P-glycoprotein inhibitior - 0.9784 97.84%
P-glycoprotein substrate - 0.9852 98.52%
CYP3A4 substrate - 0.7817 78.17%
CYP2C9 substrate - 0.5733 57.33%
CYP2D6 substrate - 0.8764 87.64%
CYP3A4 inhibition - 0.9773 97.73%
CYP2C9 inhibition - 0.9704 97.04%
CYP2C19 inhibition - 0.9700 97.00%
CYP2D6 inhibition - 0.9663 96.63%
CYP1A2 inhibition - 0.6354 63.54%
CYP2C8 inhibition - 0.9948 99.48%
CYP inhibitory promiscuity - 0.9927 99.27%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6346 63.46%
Carcinogenicity (trinary) Non-required 0.7733 77.33%
Eye corrosion + 0.9828 98.28%
Eye irritation + 0.9736 97.36%
Skin irritation + 0.8623 86.23%
Skin corrosion + 0.9753 97.53%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8100 81.00%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation - 0.7595 75.95%
Respiratory toxicity - 0.8333 83.33%
Reproductive toxicity - 0.8606 86.06%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity - 0.5546 55.46%
Acute Oral Toxicity (c) III 0.8335 83.35%
Estrogen receptor binding - 0.9578 95.78%
Androgen receptor binding - 0.9486 94.86%
Thyroid receptor binding - 0.9372 93.72%
Glucocorticoid receptor binding - 0.9388 93.88%
Aromatase binding - 0.9362 93.62%
PPAR gamma - 0.8495 84.95%
Honey bee toxicity - 0.9794 97.94%
Biodegradation + 0.8750 87.50%
Crustacea aquatic toxicity - 0.9500 95.00%
Fish aquatic toxicity - 0.5311 53.11%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL1293235 P02545 Prelamin-A/C 11220.2 nM
Potency
via CMAUP

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4040 P28482 MAP kinase ERK2 96.74% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.00% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.40% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 84.96% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.91% 99.17%

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.
Cremastra appendiculata
Pleione bulbocodioides
Pleione yunnanensis
Ranunculus ternatus

Cross-Links

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PubChem 11579
NPASS NPC7814
ChEMBL CHEMBL1235931
LOTUS LTS0104845
wikiData Q903322