キニオホン
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- hydroxyquinoline
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/06/10 00:56:32」(JST)
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Chiniofon
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| Systematic (IUPAC) name |
| 8-Hydroxy-7-iodo-5-quinolinesulfonic acid |
| Clinical data |
| AHFS/Drugs.com |
International Drug Names |
| Identifiers |
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CAS Registry Number
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547-91-1 |
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ATC code
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P01AX01 QP51AX01 |
| PubChem |
CID: 11043 |
| ChemSpider |
10575 Y |
| UNII |
98F8Y85B6W Y |
| ChEMBL |
CHEMBL2104146 |
| Chemical data |
| Formula |
C9H6INO4S |
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Molecular mass
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351.12 g/mol |
SMILES
- O=S(=O)(O)c1cc(I)c(O)c2ncccc12
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InChI
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InChI=1S/C9H6INO4S/c10-6-4-7(16(13,14)15)5-2-1-3-11-8(5)9(6)12/h1-4,12H,(H,13,14,15) Y
Key:ZBJWWKFMHOAPNS-UHFFFAOYSA-N Y
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| Y (what is this?) (verify) |
Chiniofon is an antiprotozoal agent.
External links
- Leake CD (December 1932). "The Pharmacologic Action of Chiniofon". Cal West Med 37 (6): 405–6. PMC 1658429. PMID 18742353.
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Antiparasitics – antiprotozoal agents – agents against amoebozoa/amebicide (P01)
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| Entamoeba |
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Tissue amebicides
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Nitroimidazole derivatives
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- Metronidazole#
- Tinidazole
- Ornidazole
- Nimorazole
- Secnidazole
- Azanidazole
- Propenidazole
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Other
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- isoquinoline (Emetine/Dehydroemetine)
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Luminal amebicides
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Hydroxyquinoline derivatives
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- Cl (Chlorquinaldol)
- Br (Tilbroquinol
- Broxyquinoline)
- I (Diiodohydroxyquinoline)
- I,Cl (Clioquinol)
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Dichloroacetamide derivatives
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- Diloxanide#
- Clefamide
- Etofamide
- Teclozan
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Aminoglycoside
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Other/ungrouped
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- arsenic (Arsthinol
- Difetarsone
- Glycobiarsol)
- phenanthroline (Phanquinone)
- aminoacridine (Mepacrine)
- quinazoline (Trimetrexate)
- thiazole (Tenonitrozole)
- sesquiterpene (Fumagillin)
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| Acanthamoeba |
- Propamidine
- Chlorhexidine
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- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III
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Index of protozoan infection
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| Description |
- Alveolata
- Amoebozoa
- Excavata
- Protist
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| Disease |
- Amoebozoa
- Chromalveolate
- Excavata
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| Treatment |
- Drugs
- amoeboa
- chromalveolate
- excavata
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English Journal
- Synthesis, characterization and antibacterial activity of mixed ligand dioxouranium complexes of 8-hydroxyquinoline and some amino acids.
- Patil SS, Shaikh MM.SourceDepartment of Chemistry, Changu Kana Thakur Arts, Commerce and Science College, New Panvel, Raigad, Maharashtra, India. sunilpatil_247@rediffmail.com
- Acta poloniae pharmaceutica.Acta Pol Pharm.2012 Jul-Aug;69(4):679-86.
- Mixed ligand complexes of dioxouranium(VI) of the type [UO2(Q)(L)-2H2O] have been synthesized using 8-hydroxyquinoline (HQ) as a primary ligand and N- and/or O- donor amino acids (HL) such as L-lysine, L-aspartic acid and L-cysteine as secondary ligands. The metal complexes have been characterized o
- PMID 22876610
- Disease-drug pairs revealed by computational genomic connectivity mapping on GBA1 deficient, Gaucher disease mice.
- Yuen T, Iqbal J, Zhu LL, Sun L, Lin A, Zhao H, Liu J, Mistry PK, Zaidi M.SourceThe Mount Sinai Bone Program, Mount Sinai School of Medicine, NY, USA.
- Biochemical and biophysical research communications.Biochem Biophys Res Commun.2012 Jun 15;422(4):573-7. Epub 2012 May 12.
- We have reported that, in addition to recapitulating the classical human Gaucher disease (GD1) phenotype, deletion of the glucocerebrosidase (GBA1) gene in mice results in the dysfunction of a diverse population of immune cells. Most of immune-related, non-classical features of GD1, including gammop
- PMID 22588172
Related Links
- Chiniofon. From Wikipedia, the free encyclopedia. Jump to: navigation, search. Chiniofon. Skeletal formula · Space-filling model. Systematic (IUPAC) ... Chiniofon is an antiprotozoal agent. [edit] External links. Leake CD (December 1932).
- Description, Space-filling model of the chiniofon molecule, an antiparasitic agent. This image shows the neutral form. Colour code (click to show). Black: Carbon, C: White: Hydrogen, H: Red: Oxygen, O: Blue: Nitrogen, N: Yellow: Sulfur, S ...
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