己联双辛胍二盐酸盐 T14177
品牌 | 厂商性质 | 产地 | 货期 |
---|---|---|---|
TargetMol | 生产商 | 美国 | 现货 |
性能特点
生化试剂,可用于动物细胞实验
规格 | CAS号 | 价格 | 操作 |
---|---|---|---|
5 mg | 1715-30-6 | ¥257.00 | 询底价 |
100 mg | 1715-30-6 | ¥970.00 | 询底价 |
1 mL | 1715-30-6 | ¥335.00 | 询底价 |
10 mg | 1715-30-6 | ¥367.00 | 询底价 |
25 mg | 1715-30-6 | ¥524.00 | 询底价 |
50 mg | 1715-30-6 | ¥671.00 | 询底价 |
Product Introduction
Bioactivity
英文名: Alexidine dihydrochloride
描述: Alexidine dihydrochloride 对多种真菌病原体具有抗真菌和抗生物膜活性。它是一种抗癌剂,可靶向哺乳动物细胞中的线粒体酪氨酸磷酸酶 PTPMT1,并导致线粒体凋亡。
体外活性: Alexidine dihydrochloride can decimate at low concentrations (1.5 to 6 μg/mL) mature biofilms of Candida, Cryptococcus, and Aspergillus spp. that are known to be resistant to almost all classes of antifungal drugs. Alexidine dihydrochloride displays activity against most Candida spp.; MIC values of ≤1.5 μg/mL are observed for all isolates tested under planktonic conditions, with the exception of Candida parapsilosis and Candida krusei and it also displays striking activity against clinically relevant fluconazole-resistant Candida isolates: C. albicans (CA2, CA6, and CA10), C. glabrata (CG2 and CG5), C. parapsilosis (CP5), and C. auris (CAU-09 and CAU-03)[1]. Inhibition of planktonic growth by Alexidine dihydrochloride reveals a complete inhibition of filamentation or proliferation of the imaged fungi. Alexidine dihydrochloride results in 50% killing of HUVECs and lung epithelial cells, at concentrations 5- to 10-fold higher than the MIC required to kill planktonically growing fungal pathogens[1]. In fact, at 10-fold-lower concentrations (150 ng/mL) of planktonic MICs, Alexidine dihydrochloride could inhibit lateral yeast formation and biofilm dispersal in C. albicans[1].
体内活性: Biofilm formation by C. Albicans is chosen to focus on because a murine biofilm model has been well established in this fungus and used for testing the effects of established and new antifungal agents. In fact, fungal CFU determination reveals that Alexidine dihydrochloride inhibits 67% of fungal biofilm growth and viability, compared to the control untreated biofilms[1]. The effect of the drugs on the 24-h-old biofilms growing in the jugular vein catheters of mice is visualized microscopically, which reveals significantly lower density of the biofilms in catheters treated with Alexidine dihydrochloride.
存储条件: Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度: DMSO : 250 mg/mL (429.77 mM)
关键字: anticancer | antibiofilm | Fungal | mitochondrial | AXD | antifungal | phosphatase | Alexidine Dihydrochloride | Alexidine dihydrochloride | tyrosine | inhibit | PTPMT1 | Alexidine | Apoptosis | Inhibitor
相关产品: Protosappanin B | Elesclomol | WYE-354 | Baohuoside I | Casein Kinase inhibitor A51 | Minodronic acid | Pinosylvin | FTI-277 hydrochloride | L-Glutamic acid | ZZW-115 hydrochloride
相关库: Anti-Cancer Compound Library | Mitochondria-Targeted Compound Library | Bioactive Compounds Library Max | Anti-Cancer Active Compound Library | Apoptosis Compound Library | Anti-Fungal Compound Library | NO PAINS Compound Library | Bioactive Compound Library | Anti-Infection Compound Library
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注:该产品未在中华人民共和国食品药品监督管理部门申请医疗器械注册和备案,不可用于临床诊断或治疗等相关用途