Chemodex

Nequinate

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Product Details
Synonyms Methyl benzoquate; Neqoinate; Mequinate; AY 20385; ICI 55052; Methyl 7-(benzyloxy)-6-n-butyl-4-oxo-1,4-dihydroquinoline-3-carboxylate
Product Type Chemical
Properties
Formula C22H23NO4
MW 365.42
CAS 13997-19-8
Source/Host Chemicals Synthetic
Appearance White to light yellow to brown powder.
Solubility Soluble in DMSO (10mg/ml) or ethanol (1mg/ml).
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key NNOPDLNHPOLRRE-UHFFFAOYSA-N
Smiles O=C1C2=CC(CCCC)=C(OCC3=CC=CC=C3)C=C2NC=C1C(OC)=O
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage +20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at RT.
Documents
Product Specification Sheet
Datasheet Download PDF
Description
Nequinate is a quinoline anticoccidial agent against cecal coccidiosis (Eimeria tenella) infections. It is studied for its efficacy against protozoan parasites of the genus Eimeria. The mode of action involves the inhibition of mitochondrial electron transport in the parasites, such as inhibiting xanthine oxidoreductase (XOD) activity, thus disrupting the energy metabolism. Anticoccidial drugs are a class of compounds used to prevent or treat coccidiosis, an intestinal disease caused by protozoan parasites of the genus Eimeria (and occasionally Isospora) in animals, particularly poultry and livestock. Nequinate serves as a reference compound in pharmacological and biochemical studies exploring quinoline-based inhibitors of protozoan metabolism. Compound can be used as analytical reference material.
Product References
(1) D.K. McLoughlin & M.B. Chute; Avian Dis. 17, 717 (1973) | (2) G.H. Merson, et al.; Analyst 110, 761 (1985) | (3) R.B. Williams; Int. J. Parasitol. 27, 101 (1997) | (4) Y. Niu, et al.; J. Pharmacol. Sci. 135, 114 (2017) | (5) S. Noack, et al.; Parasitol. Res. 118, 2009 (2019)
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