Phanquinone

Not to be confused with Phenanthrenequinone.

Phanquinone
Systematic (IUPAC) name


4,7-phenanthroline-5,6-dione
Identifiers
CAS Number	84-12-8^N
ATC code	P01AX04 (WHO) QP51AX03
PubChem	CID 6764
ChemSpider	6506^Y
UNII	ID94IS6N8J^Y
KEGG	D07359^Y
ChEBI	CHEBI:59141^Y
ChEMBL	CHEMBL531048^Y
Chemical data
Formula	C₁₂H₆N₂O₂
Molar mass	210.188 g/mol
SMILES O=C3c1ncccc1c2c(nccc2)C3=O
InChI InChI=1S/C12H6N2O2/c15-11-9-7(3-1-5-13-9)8-4-2-6-14-10(8)12(11)16/h1-6H^Y Key:VLPADTBFADIFKG-UHFFFAOYSA-N^Y
^NY (what is this?) (verify)

Phanquinone is an organic compound. It is a yellowish solid derived by oxidation of phenanthroline.

It has been investigated as both antiprotozoal agent and for its bactericidal activity .^[1]

References

↑ Mett H, Gyr K, Zak O, Vosbeck K (July 1984). "Duodeno-pancreatic secretions enhance bactericidal activity of antimicrobial drugs". Antimicrob. Agents Chemother. 26 (1): 35–8. doi:10.1128/aac.26.1.35. PMC 179912. PMID 6236746.

Antiparasitics – antiprotozoal agents – agents against amoebozoa/amebicide (P01)

Entamoeba

Tissue amebicides

Nitroimidazole derivatives	Metronidazole^# Tinidazole Ornidazole Nimorazole Secnidazole Azanidazole Propenidazole

Other	isoquinoline (Emetine/Dehydroemetine)

Luminal amebicides

Hydroxyquinoline derivatives	Cl (Chlorquinaldol) Br (Tilbroquinol Broxyquinoline) I (Diiodohydroxyquinoline) I, Cl (Clioquinol) related: Chiniofon

Dichloroacetamide derivatives	Diloxanide^# Clefamide Etofamide Teclozan

Aminoglycoside	Paromomycin

Other/ungrouped

Acanthamoeba

^#WHO-EM
^‡Withdrawn from market
Clinical trials:
- ^†Phase III
- ^§Never to phase III

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