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<span title="International nonproprietary name (INN): <nowiki>Quinfamide</nowiki>">Quinfamide
Bayanan asibiti
Hanyoyin gudanarwa
Magana
Lambar ATC
  • Babu
Bayyanawa
Sunan IUPAC
  • [1- (2,2-dichloroacetyl) -3,4-dihydro-2H-quinolin-6-yl] furan-2-carboxylate
Lambar CAS
[./PubChem#<span style= <abbr title="<nowiki>Compound ID</nowiki>">CID" rel="mw:WikiLink" title="PubChem">PubChem] CID
ChemSpider
UNII
KEGG
CompTox Dashboard (<abbr title="<nowiki>U.S. Environmental Protection Agency</nowiki>">EPA)
<span title="echa.europa.eu">ECHA InfoCard</span> 100.057.690Edit this at Wikidata
Bayanan sunadarai da na jiki
Tsarin C16H13Cl2NO4
Ma'auni na ƙuƙwalwa 354.18 g·mol-1 −1
Tsarin 3D (JSmol)
Rashin kunya
  • C1CC2=C (C=CC (=C2) OC (=O) C3=CC=CO3) N (C1) C (=O) C (Cl) Cl
InChI
  • I ☒=1S/C16H13Cl2NO4/c17-14 (18) 15 (20) 19-7-1-3-10-9-11 (5-6-12 (10) 19) 23-16 (21) 13-4-2-8-22-13/h2,4-6,8-9,14H,1,3,7H2 N
  • Maɓalli:SBJGFIXQRZOVTO-UHFFFAOYSA- ☒
 ☒check  (mece wannan?)   (Gaskiya)

Quinfamide magani ne wanda ke da kaddarorin rigakafi.[1]

Quinfamide yana ɗaya daga cikin ƙananan iyali na mahaɗan antiamoebic waɗanda ke ƙunshe da aikin dichloroacetamide. [ana buƙatar ƙa'ida][ana buƙatar hujja][<span title="This claim needs references to reliable sources. (December 2022)">citation needed</span>]

Quinfamide synthesis: [2]

Haɗin ya fara ne ta hanyar haɗuwa da 6-hydroxytetrahydroquinoline tare da dichloroacetyl chloride. An kammala jerin ta hanyar acylation tare da 2-furoyl chloride.

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  1. Davila-Gutierrez CE, Vasquez C, Trujillo-Hernandez B, Huerta M (March 2002). "Nitazoxanide compared with quinfamide and mebendazole in the treatment of helminthic infections and intestinal protozoa in children". The American Journal of Tropical Medicine and Hygiene. 66 (3): 251–4. doi:10.4269/ajtmh.2002.66.251. PMID 12139216.
  2. Bailey DM, Mount EM, Siggins J, Carlson JA, Yarinsky A, Slighter RG (May 1979). "1-(Dichloroacetyl)-1,2,3,4-tetrahydro-6-quinolinol esters. New potent antiamebic agents". Journal of Medicinal Chemistry. 22 (5): 599–601. doi:10.1021/jm00191a031. PMID 458814.