Decoquinate

Decoquinate
Clinical data

AHFS/Drugs.com	International Drug Names
ATCvet code	QP51AX14 (WHO)
Identifiers
IUPAC name 6-Decoxy-7-ethoxy-4-oxo-1H-quinoline-3-carboxylic acid ethyl ester
CAS Number	18507-89-6^Y
PubChem (CID)	29112
ChemSpider	27081^N
UNII	534I52PVWH^N
KEGG	D03667^Y
ChEMBL	CHEMBL416230^N
ECHA InfoCard	100.038.521
Chemical and physical data
Formula	C₂₄H₃₅NO₅
Molar mass	417.54 g/mol
3D model (Jmol)	Interactive image
SMILES CCCCCCCCCCOC1=C(C=C2C(=C1)C(=O)C(=CN2)C(=O)OCC)OCC
InChI InChI=1S/C24H35NO5/c1-4-7-8-9-10-11-12-13-14-30-21-15-18-20(16-22(21)28-5-2)25-17-19(23(18)26)24(27)29-6-3/h15-17H,4-14H2,1-3H3,(H,25,26)^N Key:JHAYEQICABJSTP-UHFFFAOYSA-N^N
^NY (what is this?) (verify)

Decoquinate is a coccidiostat used in veterinary medicine.

Synthesis

Decoquinate synthesis:^[1]

Da Cruz, F. P.; Martin, C.; Buchholz, K.; Lafuente-Monasterio, M. J.; Rodrigues, T.; Sönnichsen, B.; Moreira, R.; Gamo, F.-J.; Marti, M.; Mota, M. M.; Hannus, M.; Prudêncio, M. (2012). "Drug Screen Targeted at Plasmodium Liver Stages Identifies a Potent Multistage Antimalarial Drug". Journal of Infectious Diseases. 205 (8): 1278–86. doi:10.1093/infdis/jis184. PMC 3308910. PMID 22396598.

↑ J. J. Ball, M. Davis, J. N. Hodgson, J. M. S.Lucas, E. W. Parnell, B. W. Sharp and D.Warburton, Chem. Ind., 56 (1970).

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