Narasin (sodium salt)

CAS No. 58331-17-2

Narasin (sodium salt)( HainanMycin | naransin sodium | Naracin sodium salt )

Catalog No. M27432 CAS No. 58331-17-2

Narasin induces tumor necrosis factor-related apoptosis-induced ligand (TRAIL)-mediated apoptosis by ER stress in glioma cells and inhibits NF-κB signaling by suppressing the phosphorylation of IκBα.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 358 In Stock
5MG 491 In Stock
25MG 1890 In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Narasin (sodium salt)
  • Note
    Research use only, not for human use.
  • Brief Description
    Narasin induces tumor necrosis factor-related apoptosis-induced ligand (TRAIL)-mediated apoptosis by ER stress in glioma cells and inhibits NF-κB signaling by suppressing the phosphorylation of IκBα.
  • Description
    Narasin induces tumor necrosis factor-related apoptosis-induced ligand (TRAIL)-mediated apoptosis by ER stress in glioma cells and inhibits NF-κB signaling by suppressing the phosphorylation of IκBα.(In Vitro):Narasin caused suicidal erythrocyte death or eryptosis. In human erythrocytes, Narasin increased annexin-V-binding indicating cell membrane scrambling with phosphatidylserine translocation to the erythrocyte surface and the decrease of forward scatter reflecting cell shrinkage, which indicated the death of erythrocyte. (In Vivo):Administration of 4-48 p.p.m of narasin in the pelleted feed of New Zealand White rabbits. After 4 weeks, narasin protected rabbits from severe coccidiosis induced by E. flavescens, E. perforans E. Magna, E. Intestinalis, and E. Stiedai. In addition, narasin reduced oocyst output effectively.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    HainanMycin | naransin sodium | Naracin sodium salt
  • Pathway
    Apoptosis
  • Target
    NF-κB
  • Recptor
    ——
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    58331-17-2
  • Formula Weight
    787.01
  • Molecular Formula
    C43H71NaO11
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    CC[C@@H](C([O-])=O)[C@H]1[C@@H](C)C[C@H](C)[C@H]([C@H]([C@H](O)[C@@H](C([C@@H]([C@@H]2[C@@H](C)C[C@@H](C)[C@@]3(C=C[C@@H](O)[C@]4(CC[C@@](C)([C@H]5CC[C@@](CC)(O)C(C)O5)O4)O3)O2)CC)=O)C)C)O1.[Na+]
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Da-Wa ZM, et al. Chemical Constituents from Przewalskia tangutica. Zhong Yao Cai. 2016 Sep;39(9):2013-5.
molnova catalog
related products
  • Scandoside

    Scandoside, a cyclic enolide that can be isolated from Haemophilus difficile, exhibits anti-inflammatory activity, inhibits the expression levels of inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), TNF-α, and IL-6 messenger RNA (mRNA), and inhibits the nuclear transcription factor, kappa-B alpaha (IκB-α), p38, extracellular signal-regulated kinase (ERK) and c-Jun N-terminal kinase (JNK) inhibitor phosphorylation.

  • Gue1654

    Gue1654 is a selective OXE-R inhibitor that attenuates coronary artery ligation-induced ischemic myocardial injury and cardiomyocyte oxygen/glucose deprivation-induced injury in mice through activation of BCAT1.

  • Urolithin B

    Urolithin B inhibits NF-κB activity by reducing the phosphorylation and degradation of IκBα, and suppresses the phosphorylation of JNK, ERK, and Akt, and enhances the phosphorylation of AMPK.?Urolithin B is also a regulator of skeletal muscle mass.Urolithin B is one of the gut microbial metabolites of ellagitannins, and has anti-inflammatory and antioxidant effects.