Nevadensin

CAS No. 10176-66-6

Nevadensin ( —— )

Catalog No. M21842 CAS No. 10176-66-6

Nevadensin is a naturally occurring selective inhibitor of human carboxylesterase 1 (hCE1) with an IC50 of 2.64 μM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 51 In Stock
5MG 37 In Stock
10MG 61 In Stock
25MG 109 In Stock
50MG 175 In Stock
100MG 263 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Nevadensin
  • Note
    Research use only, not for human use.
  • Brief Description
    Nevadensin is a naturally occurring selective inhibitor of human carboxylesterase 1 (hCE1) with an IC50 of 2.64 μM.
  • Description
    Nevadensin is a naturally occurring selective inhibitor of human carboxylesterase 1 (hCE1) with an IC50 of 2.64 μM. Nevadensin has a variety of pharmacological effects such as anti-mycobacterium tuberculosis activities, antitussive, anti-inflammatory and anti-hypertensive.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    GPCR/G Protein
  • Target
    Antibacterial
  • Recptor
    IC50: 2.64 μM (hCE1), 132.8 μM (hCE2)
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    10176-66-6
  • Formula Weight
    344.32
  • Molecular Formula
    C??H??O?
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 14.71 mg/mL (42.72 mM)
  • SMILES
    O=C1C=C(C2=CC=C(OC)C=C2)OC3=C(OC)C(O)=C(OC)C(O)=C13
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

molnova catalog
related products
  • Sodium citrate dihyd...

    Sodium citrate dihydrate is an anticoagulant, and also used as a buffer and food preservatives.

  • Cefamandole nafate

    Cefamandole nafate is a second-generation broad-spectrum cephalosporin antibiotic.

  • Icariside I

    Icariin is isolated from Epimedium herb. It can stimulate osteogenic differentiation of BMSCs and inhibit bone resorption activity of osteoclasts.