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Supplier NameMedChemExpress (MCE)
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Product NameDL-Mevalonic acid lactone
SynonymsBeta-Hydro
mevalonic lactone
DL-MEVALONOLACTONE
DL-Mevalonolactone
()-Mevalonolactone
DL-Mevalonic acid lactone
D,L-Mevalonic Acid delta-Lactone

Synonyms

Beta-Hydro
mevalonic lactone
DL-MEVALONOLACTONE
DL-Mevalonolactone
()-Mevalonolactone
DL-Mevalonic acid lactone
D,L-Mevalonic Acid delta-Lactone
dl-mevalonic acid lactone, salt-free
4-hydroxy-4-methyltetrahydro-2H-pyran-2-one
(S)-4β-Hydroxy-4-methyltetrahydro-2H-pyran-2-one
(S)-Tetrahydro-4-hydroxy-4-methyl-2H-pyran-2-one
(4S)-4-Hydroxy-4-methyltetrahydro-2H-pyran-2-one
(S)-3,5-Dihydroxy-3-methylpentanoic acid δ-lactone
(±)-Mevalonolactone,(±)-β-Hydroxy-β-methyl-δ-valerolactone, (±)-3-Hydroxy-3-methyl δ-valerolactone, DL-Mevalolactone, DL-Mevalonic acid lactone
β-Hydroxy-β-methyl-δ-valerolactone, (±)-β-Hydroxy-β-methyl-δ-valerolactone, (±)-3-Hydroxy-3-methyl δ-valerolactone, (±)-Mevalolactone, (±)-Mevalonic acid lactone, (±)-Mevalonolactone
CAS674-26-0
EINECS211-615-0
Chemical FormulaC6H10O3
Molecular Weight130.14
inchiInChI=1/C6H10O3/c1-6(8)2-3-9-5(7)4-6/h8H,2-4H2,1H3
Package10 mM * 1 mL;100 mg;250 mg;500 mg
PriceGet quote
DescriptionsDL-Mevalonolactone

DL-Mevalonolactone

MedChemExpress (MCE)

HY-107855

674-26-0

(±)-Mevalonolactone

Descriptions

DL-Mevalonolactone

DL-Mevalonolactone

MedChemExpress (MCE)

HY-107855

674-26-0

(±)-Mevalonolactone
Mevalolactone

99.15%

Pure form -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month

Room temperature in continental US
may vary elsewhere.

DL-Mevalonolactone ((±)-Mevalonolactone
Mevalolactone) is the δ-lactone form of mevalonic acid, a precursor in the mevalonate pathway. DL-Mevalonolactone is orally active against HMGCR mutation and statin caused myopathy. DL-Mevalonolactone induces inflammation and oxidative stress response with decreased mitochondrial membrane potential (MMP) and induces mitochondrial swelling[2][4].

DL-Mevalonolactone (0.1-1 mM, 0-72 h) induces inflammatory response with upregulated IL1B expression,induces oxidative stress with mitochondrial membrane depolarization and increased levels of SOD2, HemeOX and ROS[4]. DL-Mevalonolactone(1-2 mM) promotes peroxidation, inhibits activity of aconitase in brain[2].

DL-Mevalonolactone exhibits efficacy against statin induced myopathy in C57BL/6 mice (200 mg/kg, p.o. for 14 days), without toxicity (2 g/kg, p.o. for 7 days)[3].

Human Endogenous Metabolite

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[1]. Domingos SR, et al. On the structural intricacies of a metabolic precursor: Direct spectroscopic detection of water-induced conformational reshaping of mevalonolactone. J Chem Phys. 2017 Sep 28
147(12):124310.
[Content Brief]

[2]. Cecatto C, et al. Mevalonolactone disrupts mitochondrial functions and induces permeability transition pore opening in rat brain mitochondria: Implications for the pathogenesis of mevalonic aciduria. Neurochem Int. 2017 Sep
108:133-145.
[Content Brief]

[3]. Yogev Y, et al., Limb girdle muscular disease caused by HMGCR mutation and statin myopathy treatable with mevalonolactone. Proc Natl Acad Sci U S A. 2023 Feb 14
120(7):e2217831120.
[Content Brief]

[4]. Gratton R, et al., Prolonged treatment with mevalonolactone induces oxidative stress response with reactive oxygen species production, mitochondrial depolarization and inflammation in human glioblastoma U-87 MG cells. Neurochem Int. 2018 Nov
120:233-237.
[Content Brief]

Supplier Websitehttps://www.medchemexpress.com/dl-mevalonolactone.html
Last Update2025-05-21 16:50:25
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