In Vitro and in Vivo Activities of HQQ-3, a New Triazole Antifungal Agent(Pharmacology)
スポンサーリンク
概要
- 論文の詳細を見る
The activity of HQQ-3, a new triazole antifungal agent, was evaluated and compared with those of fluconazole, ketoconazole and terbinafine in vitro and with fluconazole in vivo. HQQ-3 exhibited potent in vitro activity against clinically important fungi. The activity of HQQ-3 against Candida spp. was superior to those of fluconazole and terbinafine and comparable or superior to that of ketoconazole. HQQ-3 retained potent activity against Candida albicans strains with low levels of susceptibility to fluconazole (fluconazole MIC_<80>s range, 4 to >64μg/ml). Against Cryptococcus neoformans and filamentous fungi, the activity of HQQ-3 was superior to that of fluconazole. HQQ-3 also exhibited potent in vivo activity against murine systemic infections caused by C. albicns and C. krusei. The 50% effective doses against these infections were 0.12 to 1.9mg/kg of body weight. These result suggest that HQQ-3 may be useful in the treatment of candidiasis.
- 公益社団法人日本薬学会の論文
- 2006-10-01
著者
-
Liu Wen-xia
Department Of Pharmacology College Of Pharmacy Second Military Medical University
-
Cao Yong
Department Of Pharmacology School Of Pharmacy Second Military Medical University
-
Gao Ping
Department Of Pharmacology School Of Pharmacy Second Military Medical University
-
Zhao Jing-xia
Department Of Pharmacology College Of Pharmacy Second Military Medical University
-
Jiang Yuan
Department Of Pharmacology School Of Pharmacy Second Military Medical University
-
He Qiu-qing
Department Of Organic Chemistry College Of Pharmacy Second Military Medical University
-
Wu Qiu-ye
Department Of Organic Chemistry College Of Pharmacy Second Military Medical University
-
Liu Chao-mei
Department Of Organic Chemistry College Of Pharmacy Second Military Medical University
-
Gao Ping-Hui
Department of Pharmacology, School of Pharmacy, Second Military Medical University
-
Cao Ying-Ying
Department of Pharmacology, School of Pharmacy, Second Military Medical University
-
Cao Yong-Bing
Department of Pharmacology, School of Pharmacy, Second Military Medical University
-
Jiang Yuan-Ying
Department of Pharmacology, School of Pharmacy, Second Military Medical University
-
QUAN Hua
Department of Pharmacology, College of Pharmacy, Second Military Medical University
-
Quan Hua
Department Of Pharmacology College Of Pharmacy Second Military Medical University
-
Cao Ying
School Of Pharmacy Second Military Medical University
-
Cao Yong-bing
School Of Pharmacy Second Military Medical University
-
Gao Ping-hui
School Of Pharmacy Second Military Medical University
関連論文
- In Vitro and in Vivo Antifungal Activities of the Eight Steroid Saponins from Tribulus terrestris L. with Potent Activity against Fluconazole-Resistant Fungal(Pharmacology)
- A Novel Silver-Silica Catalyst Used for the Manufacture of Formaldehyde
- In Vitro Antifungal Activity of ZJ-522, a New Triazole Restructured from Fluconazole and Butenafine, against Clinically Important Fungi in Comparison with Fluconazole and Butenafine(Pharmacology)
- 乳酸菌ゲノムにコードされるクオーラムセンシングに関与する三分子制御系の遺伝子解析
- Highly Efficient Ni-Ce-O Mixed Oxide Catalysts via Gel-coprecipitation of Oxalate Precursors for Catalytic Combustion of Methane
- A Remarkable Effect of Alkali Addition in the Oxidative Carbonylation of Methanol to Dimethyl Carbonate Catalyzed by a Polymer-complexed Cu(II) Catalyst System
- Fcr1p Inhibits Development of Fluconazole Resistance in Candida albicans by Abolishing CDR1 Induction(Pharmacology)
- High-Frequency Genetic Contents Variations in Clinical Candida albicans Isolates
- Trehalose Is an Important Mediator of Cap1p Oxidative Stress Response in Candida albicans(Microbiology)
- In Vitro Synergism of Fluconazole and Baicalein against Clinical Isolates of Candida albicans Resistant to Fluconazole(Microbiology)
- Chemical Synthesis and Biological Activity of The Gelatinase Biosynthesis-Activating Pheromone of Enterococcus faecalis and Its Analogs(Organic Chemistry)
- In Vitro and in Vivo Activities of HQQ-3, a New Triazole Antifungal Agent(Pharmacology)
- Lymphtoxin β Receptor-Ig Protects from T-Cell-Mediated Liver Injury in Mice through Blocking LIGHT/HVEM Signaling(Pharmacology)