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
200MG Get Quote Get Quote
500MG 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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