4-Hydroxybutyric Acid

Details

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Internal ID a5ce080a-0c44-4687-86b5-f9b7855faf52
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Hydroxy fatty acids
IUPAC Name 4-hydroxybutanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C4H8O3/c5-3-1-2-4(6)7/h5H,1-3H2,(H,6,7)
InChI Key SJZRECIVHVDYJC-UHFFFAOYSA-N
Popularity 3,433 references in papers

Physical and Chemical Properties

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Molecular Formula C4H8O3
Molecular Weight 104.10 g/mol
Exact Mass 104.047344113 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP -0.60
Atomic LogP (AlogP) -0.16
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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4-Hydroxybutyric acid
gamma-Hydroxybutyric acid
591-81-1
4-hydroxy-butyric acid
Anetamin
4-hydroxy-butanoic acid
oxy-n-butyric acid
Butyric acid, 4-hydroxy-
3-carboxypropoxy acid
4-Hydroxyalkanoic 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 4-Hydroxybutyric Acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9325 93.25%
Caco-2 + 0.5567 55.67%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.8081 80.81%
OATP2B1 inhibitior - 0.8453 84.53%
OATP1B1 inhibitior + 0.9315 93.15%
OATP1B3 inhibitior + 0.9482 94.82%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9634 96.34%
P-glycoprotein inhibitior - 0.9886 98.86%
P-glycoprotein substrate - 0.9897 98.97%
CYP3A4 substrate - 0.7922 79.22%
CYP2C9 substrate - 0.5816 58.16%
CYP2D6 substrate - 0.8592 85.92%
CYP3A4 inhibition - 0.9611 96.11%
CYP2C9 inhibition - 0.9459 94.59%
CYP2C19 inhibition - 0.9679 96.79%
CYP2D6 inhibition - 0.9720 97.20%
CYP1A2 inhibition - 0.8816 88.16%
CYP2C8 inhibition - 0.9844 98.44%
CYP inhibitory promiscuity - 0.9789 97.89%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.7131 71.31%
Eye corrosion + 0.8799 87.99%
Eye irritation + 0.9859 98.59%
Skin irritation + 0.5404 54.04%
Skin corrosion + 0.9520 95.20%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8119 81.19%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.8125 81.25%
skin sensitisation - 0.9379 93.79%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity - 0.9000 90.00%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.6426 64.26%
Acute Oral Toxicity (c) III 0.6543 65.43%
Estrogen receptor binding - 0.9508 95.08%
Androgen receptor binding - 0.9307 93.07%
Thyroid receptor binding - 0.9383 93.83%
Glucocorticoid receptor binding - 0.8767 87.67%
Aromatase binding - 0.7901 79.01%
PPAR gamma - 0.8437 84.37%
Honey bee toxicity - 0.9864 98.64%
Biodegradation + 0.9000 90.00%
Crustacea aquatic toxicity - 1.0000 100.00%
Fish aquatic toxicity - 0.9094 90.94%

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 91.59% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.41% 99.17%
CHEMBL2581 P07339 Cathepsin D 83.44% 98.95%
CHEMBL1781 P11387 DNA topoisomerase I 81.22% 97.00%

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.
Arabidopsis thaliana
Lotus corniculatus

Cross-Links

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PubChem 10413
LOTUS LTS0101881
wikiData Q207920