ELQ-300

CAS No. 1354745-52-0

ELQ-300( —— )

Catalog No. M20214 CAS No. 1354745-52-0

ELQ-300 is bioavailable antimalarial agent acts as an inhibitor of the reductive (Qi) site of the cytochrome bc1 complex (cyt bc1).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 110 In Stock
10MG 177 In Stock
25MG 357 In Stock
50MG 530 In Stock
100MG 759 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    ELQ-300
  • Note
    Research use only, not for human use.
  • Brief Description
    ELQ-300 is bioavailable antimalarial agent acts as an inhibitor of the reductive (Qi) site of the cytochrome bc1 complex (cyt bc1).
  • Description
    ELQ-300 is bioavailable antimalarial agent acts as an inhibitor of the reductive (Qi) site of the cytochrome bc1 complex (cyt bc1).
  • In Vitro
    ELQ-300 (0-70 nM, 21 d) inhibits P. falciparum Dd2, Tm90-C2B, and D1 growth with IC50 values of 6.6, 4.6 and 160 nM, respectively.
  • In Vivo
    ELQ-300 (1 and 10 mg/kg; p.o. once daily for 1 or 4 days) inhibits P. yoelii growth in an acute infection model.ELQ-300 (10 and 20 mg/kg; p.o. once daily for 1 or 4 days) prevents recurrence of infection in mice. Animal Model:6-week female CF-1 mice with P. yoelii-WT infection Dosage:1 and 10 mg/kg Administration:Oral gavage; 1 mg/kg once daily for 4-day; 10 mg/kg once daily for 1-day Result:Inhibited P. yoelii with ED50 values of 0.04 and 0.03 mg/kg for 4-day dosing and 1-day dosing, respectively.Animal Model:6-week female CF-1 mice with P. yoelii-WT infection Dosage:10 and 20 mg/kg Administration:Oral gavage; 10 mg/kg once daily for 4-day; 20 mg/kg once daily for 1-day Result:Effectively prevented recrudescence in the 4-day dosing studies with infection mice.
  • Synonyms
    ——
  • Pathway
    Microbiology/Virology
  • Target
    Parasite
  • Recptor
    Parasite
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1354745-52-0
  • Formula Weight
    475.85
  • Molecular Formula
    C24H17ClF3NO4
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:15.62 mg/mL?(32.83 mM)
  • SMILES
    COc1cc2[nH]c(C)c(-c3ccc(Oc4ccc(OC(F)(F)F)cc4)cc3)c(=O)c2cc1Cl
  • Chemical Name
    6-Chloro-7-methoxy-2-methyl-3-{4-[4-(trifluoromethoxy)phenoxy]phenyl}quinolin-4(1H)-one

Shipping & Storage Information

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

Reference

1.Stickles AM et al. Subtle changes in endochin-like quinolone structure alter the site of inhibition within the cytochrome bc1 complex of Plasmodium falciparum. Antimicrob Agents Chemother. 2015 Apr;59(4):1977-82.
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