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  • 阿尼芬净|T6088

阿尼芬净|T6088

Anidulafungin
166663-25-8
233 1mg 起订
323 2mg 起订
519 5mg 起订
上海 更新日期:2025-03-12

TargetMol中国(陶术生物)

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产品详情:

中文名称:
阿尼芬净
英文名称:
Anidulafungin
CAS号:
166663-25-8
品牌:
TargetMol
产地:
美国
保存条件:
store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
纯度规格:
99.15%
产品类别:
抑制剂
货号:
T6088

Product Introduction

Bioactivity

名称Anidulafungin
描述Anidulafungin (Ecalta) (LY303366) is an echinocandin derivative used as an antifungal drug. It inhibits glucan synthase activity.
细胞实验Anidulafungin is dissolved in DMSO and stored, and then diluted[2]. Stocks of CD101 (formerly SP 3025, biafungin, AF-025) are prepared fresh in 100% DMSO prior to use. The comparator antifungals Anidulafungin (ANF), Caspofungin (CSF), and Amphotericin B (AMB) are also prepared in 100% DMSO. MIC assays are performed via broth microdilution in accordance with CLSI guidelines, with the exception that test compounds are made up at a 50× final assay concentration and 100 μL assay mixture volumes are used (2 μL added to 98 μL of broth containing cells at 0.5×103 to 2.5×103 CFU/mL). All MIC assays are run at least three times, and a representative data set is shown. Quality control (QC) is assessed throughout the study via comparison of MIC values derived for WT C. krusei strain ATCC 6258 for AMB, CSF, and ANF with previously reported CLSI 24-h broth microdilution QC ranges[2].
激酶实验FITC-S1P quantification/Caliper assay: A 384-well format of the SphK enzyme assay based on separation of FITC-S1P from unreacted FITC-sphingosine substrate using a microfluidic capillary electrophoresis mobility-shift system is developed. Briefly, 3 nM SphK1–His6 is incubated with 1 μM FITC-sphingosine, 20 μM ATP and 10 μM compound (a final concentration of DMSO of 2 %) in a buffer containing 100 mM Hepes (pH 7.4), 1 mM MgCl2,0.01% Triton X-100, 10% glycerol, 100 μM sodium orthovanadate and 1 mM DTT for 1 h in a 384-well Matrical MP-101-1-PP plate. Reaction mixtures (10 μL) are quenched by the addition of 20 μL of 30 mM EDTA and 0.15% Coating Reagent-3 in 100 mM Hepes, and a small aliquot of each reaction (a few nanolitres) is analysed in the Caliper LabChip 3000 instrument under -1.5 psi (psi=6.9 kPa) pressure, a downstream voltage of -1900 V and a sip time of 0.2 s. Phosphorylated fluorescent product and unphosphorylated fluorescent substrate appeared as distinctive peaks and are quantified using the Caliper data.
体外活性Anidulafungin(LY-303366)对所有测试的Candida albicans(n=99)、Candida glabrata(n=18)、Candida tropicalis(n=10)分离株的最低抑菌浓度(MIC)均≤0.32 μg/mL。Anidulafungin对Aspergillus种(90%分离株被抑制的最低有效浓度,0.02 μg/mL)亦有活性(n=20),但对Candida parapsilosis的活性较低(90%分离株被抑制的MIC [MIC90],5.12 μg/mL)(n=10),对C. neoformans(MIC90 >10.24 μg/mL)(n=15)和B. dermatitidis(MIC90,16 μg/mL)(n=29)无活性。Fluconazole对三株C. tropicalis、七株C. glabrata和两株Candida krusei的MIC均≥16 μg/mL。对这12株中的11株,Anidulafungin的MIC范围从0.08至0.32 mg/mL。第十二株为C. krusei(Fluconazole MIC,32 μg/mL),其Anidulafungin MIC为1.28 mg/mL。这12株的90%抑制MIC(MIC90)为0.32 μg/mL。对于Fluconazole MIC≥8 μg/mL的其余18株C. glabrata和C. tropicalis分离株,Anidulafungin的MIC90也是0.32 mg/mL。Anidulafungin对Fluconazole MIC ≥16 mg/mL的Candida种同对Fluconazole MIC ≥8 μg/mL的种表现出同等活性。与C. albicans、C. glabrata和C. tropicalis相比,Anidulafungin对C. neoformans和B. dermatitidis的活性显著较低。Ketoconazole和amphotericin B是对C. neoformans和B. dermatitidis测试中最活跃的抗真菌药。Anidulafungin对Aspergillus种展示出强大的体外活性,其MEC90为0.02 μg/mL。对照种酵母分离株的Anidulafungin MIC为C. albicans ATCC 90028的0.02 μg/mL,C. glabrata ATCC 90030的0.16 mg/mL,C. neoformans ATCC 90112的>10.24 μg/mL。通过CD101选择的菌株若CD101 MIC增加至少2倍,其Anidulafungin(ANF)和/或Caspofungin(CSF)的MIC也至少增加2倍。
存储条件store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
溶解度H2O : < 1 mg/mL (insoluble or slightly soluble)
DMSO : 93 mg/mL (81.6 mM)
Ethanol : < 1 mg/mL (insoluble or slightly soluble)
关键字LY-303366 | LY 303366 | Inhibitor | inhibit | Fungal | Antibiotic | Anidulafungin
相关产品Cefaclor monohydrate | Potassium gluconate | Dehydroacetic acid sodium | G-418 disulfate | Doxycycline | Neomycin sulfate | Geraniol | Metronidazole | EDTA copper(II) disodium salt | Ampicillin sodium | Sulfamethoxazole sodium | Kanamycin sulfate
相关库微生物天然产物库 | 抑制剂库 | 经典已知活性库 | 已知活性化合物库 | 抗真菌库 | 抗生素库 | 上市药物库 | FDA 上市药物库 | 大环化合物库 | 免疫/炎症分子化合物库 | 药物功能重定位化合物库 | 儿童药物库
阿尼芬净|||LY303366|||Eraxis|||Ecalta|TargetMol

公司简介

上海陶术生物科技有限公司为美国Target Molecule Corp. ( Target Mol ) 在上海建立的全资子公司。我们与美国波士顿、德国慕尼黑的同事一起,为北美、欧洲和亚洲从事药物研发和生物学研究的科学家提供优质的产品和专业的服务。公司下设筛选事业部,化学事业部,生物事业部和新材料部。 从虚拟筛选到实体化合物分子供应;从商业化产品销售到个性化定制合成;从对明确靶点的分子筛选到对明确分子的多靶点筛选,从高通量筛选到化学结构优化,我们都可以满足您的科研用品及技术服务的需求。 经过在中国市场五年的精心耕耘,我们已成为筛选化合物领域优秀的供应商,为超过五百家学校和各类企业提供了品质卓越的小分子化合物和药物筛

成立日期 (12年)
注册资本 566.2651万人民币
员工人数 100-500人
年营业额 ¥ 1亿以上
经营模式 贸易,试剂,定制,服务
主营行业 化学试剂,生物活性小分子

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