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 |
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| 10MG | 177 | In Stock |
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| 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
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Product NameELQ-300
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NoteResearch use only, not for human use.
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Brief DescriptionELQ-300 is bioavailable antimalarial agent acts as an inhibitor of the reductive (Qi) site of the cytochrome bc1 complex (cyt bc1).
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DescriptionELQ-300 is bioavailable antimalarial agent acts as an inhibitor of the reductive (Qi) site of the cytochrome bc1 complex (cyt bc1).
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In VitroELQ-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.
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In VivoELQ-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.
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Synonyms——
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PathwayMicrobiology/Virology
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TargetParasite
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RecptorParasite
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Research Area——
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Indication——
Chemical Information
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CAS Number1354745-52-0
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Formula Weight475.85
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Molecular FormulaC24H17ClF3NO4
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Purity>98% (HPLC)
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SolubilityDMSO:15.62 mg/mL?(32.83 mM)
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SMILESCOc1cc2[nH]c(C)c(-c3ccc(Oc4ccc(OC(F)(F)F)cc4)cc3)c(=O)c2cc1Cl
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Chemical Name6-Chloro-7-methoxy-2-methyl-3-{4-[4-(trifluoromethoxy)phenoxy]phenyl}quinolin-4(1H)-one
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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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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