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别名 | UK-109496 | 储存条件 (自收到货起) |
3年 / -20°C / 粉状 1年 / -80°C / 溶于溶剂 |
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化学式 | C16H14F3N5O |
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分子量 | 349.31 | CAS号 | 137234-62-9 | |
Solubility (25°C)* | 体外 | DMSO | 70 mg/mL (200.39 mM) | |
Ethanol | 70 mg/mL (200.39 mM) | |||
Water | Insoluble | |||
* <1 mg/ml means slightly soluble or insoluble. * Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. |
产品描述 | Voriconazole是类似于氟康唑和伊曲康唑的新型三唑衍生物,其作用是通过抑制真菌 cytochrome P-450 依赖性的,14-alpha-sterol demethylase 介导的 麦角固醇的合成。 | |
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靶点 |
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体外研究 | Voriconazole能够有效抵抗某些条件丝状菌和双态性真菌(霉菌)以及酵母菌。对大多测试的霉菌,除了R. arrhizus和S. schenckii,Voriconazole在体外的活性高于或类似于itraconazole和 amphotericin B。[1]Voriconazole抑制95%的菌株,在≤1 微克/毫升下,能够抵抗448中近期临床上的霉菌。[2] |
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体内研究 | 在患有肺曲菌病的免疫功能不全的豚鼠体内,Voriconazole减少其肺部曲霉属真菌含量的效果显著高于itraconazole。在实验性肺部或颅内感染C. neoformans 的豚鼠体内,Voriconazole也被证明是有效的。[1] 与对照组的组织中相比,Voriconazole (5 毫克/千克/天,腹腔注射)结合Amphotericin B (1.25毫克/千克/天,腹腔注射)显著降低选定豚鼠体内组织中的菌落数。与用caspofungin acetate (区别在统计学上不显著)处理过的豚鼠组织相比,Voriconazole (5 毫克/千克/天,腹腔注射)结合Amphotericin B (1.25毫克/千克/天,腹腔注射)也会导致组织中菌落数的减少,并且提高生存时间,但不能杀菌。Voriconazole (5 毫克/千克/天,腹腔注射)结合caspofungin acetate (CAS)在任意剂量下减少组织中菌落数,比对照组高出1,000倍,其仅显著减少阳性培养物的数量。[3] |
, Antimicrob Agents Chemother, 2015, 59(12):7205-13.
Interactions between antifungals and everolimus against Cryptococcus neoformans [ Front Cell Infect Microbiol, 2023, 13:1131641] | PubMed: 37026056 |
The Synergistic Effect of Tacrolimus (FK506) or Everolimus and Azoles Against Scedosporium and Lomentospora Species In Vivo and In Vitro [ Front Cell Infect Microbiol, 2022, 12:864912] | PubMed: 35493742 |
Synergistic effect of pyrvinium pamoate and posaconazole against Cryptococcus neoformans in vitro and in vivo [ Front Cell Infect Microbiol, 2022, 12:1074903] | PubMed: 36569209 |
Terconazole, an Azole Antifungal Drug, Increases Cytotoxicity in Antimitotic Drug-Treated Resistant Cancer Cells with Substrate-Specific P-gp Inhibitory Activity [ Int J Mol Sci, 2022, 23(22)13809] | PubMed: 36430288 |
A Preliminary in vitro and in vivo Evaluation of the Effect and Action Mechanism of 17-AAG Combined With Azoles Against Azole-Resistant Candida spp [ Front Microbiol, 2022, 13:825745] | PubMed: 35875545 |
The synergistic effect of minocycline and azole antifungal drugs against Scedosporium and Lomentospora species [ BMC Microbiol, 2022, 22(1):21] | PubMed: 35016611 |
In Vitro and In Vivo Interactions of TOR Inhibitor AZD8055 and Azoles against Pathogenic Fungi [ Microbiol Spectr, 2022, 10(1):e0200721] | PubMed: 35019705 |
Antifungal Activity of Minocycline and Azoles Against Fluconazole-Resistant Candida Species [ Front Microbiol, 2021, 12:649026] | PubMed: 34054751 |
Differential Interactome Based Drug Repositioning Unraveled Abacavir, Exemestane, Nortriptyline Hydrochloride, and Tolcapone as Potential Therapeutics for Colorectal Cancers [ Front Bioinform, 2021, 1:710591] | PubMed: 36303724 |
In vitro and in vivo Study of Antifungal Effect of Pyrvinium Pamoate Alone and in Combination With Azoles Against Exophiala dermatitidis [ Front Cell Infect Microbiol, 2020, 10:576975] | PubMed: 33194816 |
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如果需要长期保存,请于零下二十度低温保存。禁止用于人体及治疗!
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