Epi lovastatin-d3

CAT:
804-HY-N0504S-01
Size:
1 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Epi lovastatin-d3 - image 1

Epi lovastatin-d3

  • Description:

    Epi Lovastatin-d3 is the deuterium labeled Lovastatin. Lovastatin is a cell-permeable HMG-CoA reductase inhibitor used to lower cholesterol.
  • UNSPSC:

    12352005
  • Target:

    Autophagy; Ferroptosis; HMG-CoA Reductase (HMGCR) ; Isotope-Labeled Compounds
  • Related Pathways:

    Apoptosis; Autophagy; Metabolic Enzyme/Protease; Others
  • Field of Research:

    Cardiovascular Disease; Cancer
  • Solubility:

    10 mM in DMSO
  • Smiles:

    O (C ([C@@H] (CC) C ([2H]) ([2H]) [2H]) =O) [C@@H]1[C@]2 (C (C=C[C@H] (C) [C@@H]2CC[C@@H]3C[C@@H] (O) CC (=O) O3) =C[C@H] (C) C1) [H]
  • Molecular Formula:

    C24H33D3O5
  • Molecular Weight:

    407.56
  • References & Citations:

    [1]Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53 (2) :211-216. |[2]Alberts AW, et al. Discovery, biochemistry and biology of lovastatin. Am J Cardiol. 1988 Nov 11;62 (15) :10J-15J.|[3]Kah J, et al. Selective induction of apoptosis by HMG-CoA reductase inhibitors in hepatoma cells and dependence on p53 expression. Oncol Rep. 2012 Sep;28 (3) :1077-83.|[4]Frishman WH, et al. Lovastatin: an HMG-CoA reductase inhibitor for lowering cholesterol. Med Clin North Am. 1989 Mar;73 (2) :437-48.|[5]Tobert JA, et al. Lovastatin and beyond: the history of the HMG-CoA reductase inhibitors. Nat Rev Drug Discov. 2003 Jul;2 (7) :517-26.|[6]Ifergan I, et al. Statins reduce human blood-brain barrier permeability and restrict leukocyte migration: relevance to multiple sclerosis. Ann Neurol. 2006 Jul;60 (1) :45-55.
  • Shipping Conditions:

    Room temperature
  • Scientific Category:

    Isotope-Labeled Compounds
  • Clinical Information:

    No Development Reported
  • CAS Number:

    1330264-51-1