Niceritrol

CAS No. 5868-05-3

Niceritrol( Bufor | Cardiolipol | Perycit )

Catalog No. M27179 CAS No. 5868-05-3

Niceritrol is a niacin ester that reduces cholesterol and triglycerides in total plasma and in the VLD and LD lipoprotein fractions.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 145 In Stock
2MG 69 In Stock
5MG 100 In Stock
10MG 142 In Stock
25MG 255 In Stock
50MG 383 In Stock
100MG 566 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Niceritrol
  • Note
    Research use only, not for human use.
  • Brief Description
    Niceritrol is a niacin ester that reduces cholesterol and triglycerides in total plasma and in the VLD and LD lipoprotein fractions.
  • Description
    Niceritrol is a niacin ester that reduces cholesterol and triglycerides in total plasma and in the VLD and LD lipoprotein fractions.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    Bufor | Cardiolipol | Perycit
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Cathepsin L| P. falciparum
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    5868-05-3
  • Formula Weight
    556.531
  • Molecular Formula
    C29H24N4O8
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    O=C(OCC(COC(=O)c1cccnc1)(COC(=O)c1cccnc1)COC(=O)c1cccnc1)c1cccnc1
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Shah PP, et al. Kinetic characterization and molecular docking of a novel, potent, and selective slow-binding inhibitor of human cathepsin L. Mol Pharmacol. 2008 Jul;74(1):34-41.
molnova catalog
related products
  • Men 10376 TFA

    Men 10376 TFA is an effective and selective tachykinin nk-2 receptor antagonist with a K I value of 4.4 M for the nk-2 receptor in the small intestine of rats.

  • AVE 0991

    AVE 0991, a nonpeptide analog of angiotensin-(1-7) [Ang-(1-7)], is an orally active Mas agonist with inhibitory effects on [125I]-Ang-(1-7) binding to bovine aortic endothelial cell membranes, and inhibits astrocyte-mediated neuroinflammation in Alzheimer's disease by enhancing autophagy.

  • FPR A14

    FPR A14 is an agonist of formyl peptide receptor (FPR) and induces cell differentiation.