Supriya Ghosh (Editor)

Mevastatin

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ATC code
  
None

PubChem CID
  
64715

DrugBank
  
DB06693

Molar mass
  
390.513 g/mol

CAS Number
  
73573-88-3

IUPHAR/BPS
  
3031

ChemSpider
  
58262

CAS ID
  
73573-88-3

Mevastatin Mevastatin Wikipedia

Mevastatin meaning


Mevastatin (Compactin, ML-236B) is a hypolipidemic agent that belongs to the statins class.

Contents

It was isolated from the mold Penicillium citrinum by Akira Endo in the 1970s, and he identified it as a HMG-CoA reductase inhibitor, i.e., a statin. Mevastatin might be considered the first statin drug; clinical trials on mevastatin were performed in the late 1970s in Japan, but it was never marketed. The first statin drug available to the general public was lovastatin.

Mevastatin Mevastatin Wikipedia

Mevastatin has since been derivatized to the compound pravastatin, which is a pharmaceutical used in the lowering of cholesterol and preventing cardiovascular disease.

Mevastatin Mevastatin CAS 73573883 Cay10010340 Cayman

In vitro, it has antiproliferative properties.

A British group isolated the same compound from Penicillium brevicompactum, named it compactin, and published their results in 1976. The British group mentions antifungal properties with no mention of HMG-CoA reductase inhibition.

Mevastatin Mevastatin Wikipedia

High doses inhibit growth and proliferation of melanoma cells.

Biosynthesis

Mevastatin MevastatinCompactinML236BML 236BML236BCAS 73573883 Buy

Biosynthesis of mevastatin is primarily accomplished via a type 1 PKS pathway it proceeds in the PKS pathway as seen in figure 1 until it reaches a hexaketide state where it undergoes a Diels-Alder cyclization. After cyclization it continues via the PKS pathway to a nonaketide after which it is released and undergoes oxidation and dehydration. It is presumed that the oxidations are preformed by a polypeptide that is similar to cytochrome p450 monooxygenase, which is encoded by mlcC within the mevastatin gene. Lastly the biosynthesis is completed by the PKS facilitating the addition of a diketide sidechain and a methylation by SAM. Figure 1 shows mevastatin in its acid form but it can also be in the more commonly seen lactone form. This pathway was first observed in Penicillium cilrinum and was later discovered that another type of fungus, Penicillium brevicompaetum also produced mevastatin via a PKS pathway.

Pharmacology

Mevastatin Mevastatin encyclopedia article Citizendium

Sustained elevations of cholesterol in the blood increase the risk of cardiovascular disease. Mevastatin acts to lowers hepatic production of cholesterol by competitively inhibiting HMG-CoA reductase, the enzyme that catalyzes the rate-limiting step in the cholesterol biosynthesis pathway via the mevalonic acid pathway. When hepatic cholesterol levels are decreased it causes an increased uptake of low density lipoprotein (LDL) cholesterol and reduces cholesterol levels in the circulation. It has also been shown that mevastatin upregulates endothelial nitric oxide synthase (eNOS), which is essential for maintaining a healthy cardiovascular system.

Mevastatin FileMevastatinpng Wikimedia Commons

References

Mevastatin Wikipedia