Chlorquinaldol

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Chlorquinaldol

IUPAC name 5,7-dichloro-2-methyl-8-quinolinol
Identifiers
CAS number	72-80-0^Y
PubChem	6301
ChemSpider	6062^Y
KEGG	D07208^Y
ChEBI	CHEBI:74500^N
ChEMBL	CHEMBL224325^Y
ATC code	D08AH02,G01AC03, P01AA04, R02AA11
Jmol-3D images	Image 1
SMILES Clc1c(O)c2nc(ccc2c(Cl)c1)C
InChI InChI=1S/C10H7Cl2NO/c1-5-2-3-6-7(11)4-8(12)10(14)9(6)13-5/h2-4,14H,1H3^Y Key: GPTXWRGISTZRIO-UHFFFAOYSA-N^Y InChI=1/C10H7Cl2NO/c1-5-2-3-6-7(11)4-8(12)10(14)9(6)13-5/h2-4,14H,1H3 Key: GPTXWRGISTZRIO-UHFFFAOYAU
Properties
Molecular formula	C₁₀H₇Cl₂NO
Molar mass	228.07 g/mol
N (verify) (what is: Y/N?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

Chlorquinaldol is an antimicrobial agent.^[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. PMC 179912. PMID 6236746.

Antiseptics and disinfectants (D08)

Acridine derivatives

Biguanides and amidines

Phenol and derivatives

Nitrofuran derivatives

Nitrofurazone

Iodine products

Iodine/octylphenoxypolyglycolether
Povidone-iodine^#
Diiodohydroxypropane

Quinoline derivatives

Quaternary ammonium compounds

Mercurial products

Silver compounds

Silver nitrate

Alcohols

Other

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^‡Withdrawn from market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

M: INT, SF, LCT

anat/phys/devp

noco (i/b/d/q/u/r/p/m/k/v/f)/cong/tumr (n/e/d), sysi/epon

proc, drug (D2/3/4/5/8/11)

Gynecological anti-infectives and antiseptics (G01)

Antibiotics

Arsenic compounds

Acetarsol

Quinoline derivatives

Organic acids

Sulfonamides

Sulfatolamide

Antifungals

Imidazoles	Metronidazole Clotrimazole Miconazole Econazole Ornidazole Isoconazole Tioconazole Ketoconazole Fenticonazole Azanidazole Propenidazole Butoconazole Omoconazole Oxiconazole Flutrimazole

Triazoles	Terconazole

Polyenes	Nystatin Natamycin Amphotericin B

Other	Ciclopirox Methylrosaniline

Other

M: ♀ FRS

anat/phys/devp

noco/cong/npls, sysi/epon

proc/asst, drug (G1/G2B/G3CD)

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

M: PRO

ambz, excv, chrm (strc)

ambz, excv, chrm

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