03907
噻康唑
97%
别名:
1-[2-[(2-Chloro-3-thienyl)methoxy]-2-(2,4-dichlorophenyl)ethyl]-1H-imidazole, Thioconazole
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关于此项目
经验公式（希尔记法）:
C16H13Cl3N2OS
化学文摘社编号:
分子量:
387.71
PubChem Substance ID:
UNSPSC Code:
51302325
NACRES:
NA.85
EC Number:
265-973-8
MDL number:
产品名称
噻康唑, 97%
SMILES string
Clc1ccc(C(Cn2ccnc2)OCc3ccsc3Cl)c(Cl)c1
Clc1ccc(C(Cn2ccnc2)OCc3ccsc3Cl)c(Cl)c1
InChI
1S/C16H13Cl3N2OS/c17-12-1-2-13(14(18)7-12)15(8-21-5-4-20-10-21)22-9-11-3-6-23-16(11)19/h1-7,10,15H,8-9H2
InChI key
QXHHHPZILQDDPS-UHFFFAOYSA-N
assay
≥96.5% (HPLC)
96.5-103.5% (NT)
97%
form
powder
color
white to off-white
antibiotic activity spectrum
fungi
yeast
mode of action
cell membrane | interferes
Quality Level
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Application
Tioconazole was used to study the synergistic mechanisms of antifungals on Candida albicans as well as significant drug-drug interactions in vivo.
Biochem/physiol Actions
Tioconazole is an antifungal medication of the imidazole class used to treat infections caused by fungus and yeast.It is more active than fluconazole or voriconazole against Candida glabrata mutant strains. It acts by membrane disruption and loss of intracellular ATP.
General description
Chemical structure: pyrimidine
Other Notes
Keep container tightly closed in a dry and well-ventilated place. Keep in a dry place.
Packaging
10G
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 2 - Skin Sens. 1
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
A L Fachin et al.
Medical mycology, 39(1), 129-133 (2001-03-29)
The electrophoretic pattern of the intracellular esterase of the dermatophyte Trichophyton rubrum was altered when this fungus was grown in the presence of subinhibitory concentrations of the antimycotics tioconazole or griseofulvin. All strains (original isolate and antimycotic resistant mutants) presented
Jean-Paul L Marty et al.
The Journal of dermatological treatment, 16(5-6), 299-307 (2006-01-24)
To assess the daily treatment costs and the average cost-effectiveness of three topical onychomycosis therapies - amorolfine 5% and ciclopirox 8% nail lacquers and tioconazole 28% nail solution - when used as indicated in France, the UK, Germany and Italy.
Synergistic action of nikkomycin X/Z with azole antifungals on Candida albicans.
Slawomir Milewski, Fiorenzo Mignini, et. Al
Microbiology, 137, 2155-2161 (1991)
Wenjiang Zhang et al.
Drug metabolism and disposition: the biological fate of chemicals, 30(3), 314-318 (2002-02-21)
The interactions of a panel of antifungal agents with cytochromes P450 (P450s), as a means of predicting potential drug-drug interactions, have not yet been investigated. The objective of this study was to evaluate the specificity and selectivity of five antifungal
M Pereira et al.
Mycopathologia, 143(2), 71-75 (1999-04-17)
Understanding the genetic mechanisms involved in resistance to antifungal agents is important in the fight against pathogenic fungi. In the present investigation we studied a strain of the model fungus Aspergillus nidulans which presents resistance to tioconazole and behaves as
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