Date published: 2026-4-29

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Lovastatin Diol Lactone (CAS 79952-42-4)

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CAS Number:
79952-42-4
Molecular Weight:
320.42
Molecular Formula:
C19H28O4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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6(R)-[2-(8(S)-Hydroxy]-2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydro-1(S)-naphthyl]ethyl-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one functions as an inhibitor of a specific enzyme involved in the biosynthesis of a key cellular component. It achieves this by binding to the active site of the enzyme, preventing its normal substrate from binding and undergoing the usual chemical transformation. This disruption ultimately leads to a decrease in the production of the target cellular component, impacting various cellular processes. The compound′s mechanism of action involves forming specific non-covalent interactions with amino acid residues within the enzyme′s active site, effectively blocking its function. This interference at the molecular level results in downstream effects on cellular metabolism and function. The compound′s structure allows it to fit precisely into the enzyme′s active site, disrupting its normal activity and leading to the desired biological effects. 6(R)-[2-(8(S)-Hydroxy]-2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydro-1(S)-naphthyl]ethyl-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one plays a specific role in modulating cellular processes by inhibiting the activity of a key enzyme involved in the biosynthesis of a cellular component.


Lovastatin Diol Lactone (CAS 79952-42-4) References

  1. A Cost-Efficient Synthesis of Simvastatin via High-Conversion Methylation of an Alkoxide Ester Enolate  |  Rajesh K. Thaper, Yatendra Kumar, S. M. Dileep Kumar, Satyananda Misra, and Jag Mohan Khanna. 1999. Org. Proc. Res. Dev. 6: 476–479.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Lovastatin Diol Lactone, 10 mg

sc-210564
10 mg
$322.00