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Chemical Structure
Chemical Structure
Chemical Structure

Mevastatin [73573-88-3]

Research Use Only
CDX-M0183
Chemodex
CAS Number73573-88-3
Product group Chemicals
Estimated Purity>95%
Molecular Weight390.51
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Packing Size
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Overview

  • Supplier
    Chemodex
  • Product Name
    Mevastatin [73573-88-3]
  • Delivery Days Customer
    10
  • CAS Number
    73573-88-3
  • Certification
    Research Use Only
  • Estimated Purity
    >95%
  • Molecular Formula
    C23H34O5
  • Molecular Weight
    390.51
  • Scientific Description
    Chemical. CAS: 73573-88-3. Formula: C23H34O5. MW: 390.51. Mevastatin is an antibiotic that is a competitive HMG-CoA reductase inhibitor, thus suppressing Ras farnesylation. Mevastatin decreases cholesterol biosynthesis in vitro and in vivo. It induces apoptosis, arrests cancer cells in G1 phase and downregulates cdk 2, 4, and 6, cyclin D1 and E1, p21 and p27. Mevastatin also suppresses TNF-induced NF-kappaB activation and potentiates apoptosis in human myeloid leukemia cells. Mevastatin induced neurite outgrowth of neuroblastoma cells via activation of EGFR, ERK1/2 and Akt/PBK but also exerts a neurotoxic effect in cultured neurons in a heme-independent manner. Mevastatin also shows antileishmanial and antifungal activity. Has also anti-inflammatory effects potentially via up-regulation of heme oxygenase-1 (HO-1). - Mevastatin is an antibiotic that is a competitive HMG-CoA reductase inhibitor, thus suppressing Ras farnesylation. Mevastatin decreases cholesterol biosynthesis in vitro and in vivo. It induces apoptosis, arrests cancer cells in G1 phase and downregulates cdk 2, 4, and 6, cyclin D1 and E1, p21 and p27. Mevastatin also suppresses TNF-induced NF-kappaB activation and potentiates apoptosis in human myeloid leukemia cells. Mevastatin induced neurite outgrowth of neuroblastoma cells via activation of EGFR, ERK1/2 and Akt/PBK but also exerts a neurotoxic effect in cultured neurons in a heme-independent manner. Mevastatin also shows antileishmanial and antifungal activity. Has also anti-inflammatory effects potentially via up-regulation of heme oxygenase-1 (HO-1).
  • SMILES
    [H][C@@]12C(C=C[C@H](C)[C@]2([H])CC[C@@]3([H])OC(C[C@@](O)([H])C3)=O)=CCC[C@@H]1OC([C@@H](C)CC)=O
  • Storage Instruction
    2°C to 8°C
  • UNSPSC
    12352200