计算溶液所需的质量、体积或浓度。
概述
Information
Miconazole Nitrate Miconazole (NSC 169434) Nitrate is an imidazole antifungal agent by inhibiting ergosterol biosynthesis and inducing ROS, used to treat vaginal yeast infections.
In vitro
Miconazole induces changes in the actin cytoskeleton, indicative of increased filament stability, prior to ROS induction. Miconazole disrupts steroidogenesis in Leydig and adrenal cells by inhibiting 17alpha-hydroxylase/17,20-lyase (P450c17) enzyme activity, thus reducing the conversion of progesterone to androstenedione. Miconazole reversibly inhibits (Bu)(2)cAMP-stimulated progesterone production in a dose- and time-dependent manner in MA-10 cells without affecting total protein synthesis or P450(scc) and 3beta-hydroxysteroid dehydrogenase (3beta-HSD) enzyme expression or activity. Miconazole is known to interfere with the synthesis of fungal and bacterial lipid membranes as it restrains the synthesis of Ergosterol which results in accumulation of toxic methylated sterol intermediates in membranes and subsequently in fungal cell growth arrests. Miconazole induces actin cytoskeleton stabilization in Saccharomyces cerevisiae prior to induction of reactive oxygen species, pointing to an ancillary mode of action. Miconazole treatment releases Ca(2+) from the thapsigargin (TG)-sensitive ER pool of WEHI7.2 cells. Miconazole induces apoptosis, based on morphological and biochemical criteria, and on inhibition by the Bcl-2 oncogene. Miconazole–induced intracellular Ca(2+) changes is inhibited by overexpression of Bcl-2. Miconazole induces apoptosis in the glucocorticoid sensitive and resistant human T-cell leukemia lines, CEM-C7 and CEM-C1 respectively, in normal thymocytes and in normal lymphocytes, in addition to inducing cell death in WEHI7.2 cells.
In vivo
Cell Data
cell lines：MCF-7, MCNeuA
Concentrations：
Incubation Time：
Powder Purity:≥99%
规格
英文别名
NSC 169434 Nitrate
规格或纯度
10mM in DMSO
英文名称
Miconazole Nitrate
生化机理
硝酸咪康唑（NSC 169434）是一种咪唑类抗真菌剂，通过抑制麦角甾醇的生物合成和诱导 ROS，用于治疗阴道酵母菌感染。
储存条件
-80℃储存
运输条件
特低温运输
作用类型
抑制剂
作用机制
细胞色素 P450 51 抑制剂
名称和识别符
EC号
245-256-6
分子类型
小分子
Isomeric SMILES
C1=CC(=C(C=C1Cl)Cl)COC(CN2C=CN=C2)C3=C(C=C(C=C3)Cl)Cl.[N+](=O)(O)[O-]
PubChem CID
分子量
479.14
Reaxy-Rn
4225531
高级数据
化学和物理性质
溶解性
Solubility (25°C) In vitro DMSO: 100 mg/mL (155.35 mM); Ethanol: 15 mg/mL (23.3 mM); Water: Insoluble;
熔点
184 °C(dec.)
安全和危险性（GHS）
信号词
警告
危险声明
H227: 可燃液体
预防措施声明
P210: 远离热源，热表面，火花，明火和其他点火源。 - 禁止抽烟。
P280: 戴防护手套/穿防护服/戴防护眼罩/戴防护面具。
P370+P378: 火灾时：使用干砂、干粉或抗醇泡沫灭火。
P403: 存放在通风良好的地方。
P501: 将内容物/容器送到批准的废物处理厂处理
WGK Germany
3
RTECS
NI4771000
Merck Index
6178
个人防护装备
dust mask type N95 (US),Eyeshields,Faceshields,Gloves
质检证书(CoA,COO,BSE/TSE 和分析图谱)
C of A & Other Certificates(BSE/TSE, COO):
输入批号以搜索分析图谱:
此产品的引用文献
溶液计算器
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