NQTrp

CAS No. 185351-19-3

NQTrp( —— )

Catalog No. M27509 CAS No. 185351-19-3

NQTrp is an inhibitor of the aggregation of the tau protein with generic anti-amyloidogenic effects.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 108 Get Quote
10MG 169 Get Quote
25MG 309 Get Quote
50MG 465 Get Quote
100MG Get Quote Get Quote
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Biological Information

  • Product Name
    NQTrp
  • Note
    Research use only, not for human use.
  • Brief Description
    NQTrp is an inhibitor of the aggregation of the tau protein with generic anti-amyloidogenic effects.
  • Description
    NQTrp is an inhibitor of the aggregation of the tau protein with generic anti-amyloidogenic effects.(In Vitro):NQTrp inhibits the in vitro aggregation of hexapeptide (41GCWMLY46 within the N-terminus of γD-crystallin) as well as full-length γD-crystallin. NQTrp effectively inhibits the fibrillation of the GDC6 peptide (50 μM) in a dose-dependent manner and prevents the formation of elongated amyloid fibrils. NQTrp has no toxic effect toward retinal cell culture and reduces the cytotoxicity induced by aggregates of the hexapeptide(IC50=70 μM) in ARPE-19 cells. In TEM analysis, GDC6 peptide fibrils (50 μM) in the presence of NQTrp 5:1, 1:1, 1:5 ratio (GDC6: NQTrp).
  • In Vitro
    In TEM analysis, GDC6 peptide fibrils (50 μM) in the presence of NQTrp 5:1, 1:1, 1:5 ratio (GDC6: NQTrp). NQTrp effectively inhibits the fibrillation of the GDC6 peptide (50 μM) in a dose-dependent manner and prevents the formation of elongated amyloid fibrils.NQTrphas no toxic effect toward retinal cell culture and reduces the cytotoxicity induced by aggregates of the hexapeptide(IC50=70 μM) in ARPE-19 cells.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Cytoskeleton/Cell Adhesion Molecules
  • Target
    Microtubule/Tubulin
  • Recptor
    Platelet aggregation
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    185351-19-3
  • Formula Weight
    360.36
  • Molecular Formula
    C21H16N2O4
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 125 mg/mL (346.88 mM)
  • SMILES
    OC([C@H](Cc1c[nH]c2c1cccc2)NC(C(c1c2cccc1)=O)=CC2=O)=O
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Wang Shaojie, et al. Preparation of imidazole derivatives as platelet aggregation inhibitors. CN114105881A
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