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Ciclopirox, 铝螯合剂

Fungal Inhibitors
  • CAS编号: 29342-05-0
  • 分子式: C12H17NO2
  • 分子量: 207.27
有货

库存信息

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货号 (SKU) 包装规格 是否现货 价格 数量
C408974-1ml
1ml 现货 Stock Image
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Compound libraries (12333)

基本描述

别名 环吡酮
英文别名 6-​cyclohexyl-​1-​hydroxy-​4-​methyl-2(1H)​-​pyridinone
规格或纯度 Moligand™, 10mM in DMSO
英文名称 Ciclopirox
生化机理 环吡酮胺是一种广谱抗真菌剂,具有铁螯合剂的作用。
储存温度 -80℃储存
运输条件 超低温冰袋运输
作用类型 抑制剂
作用机制 铝螯合剂
产品介绍


Information

Ciclopirox Ciclopirox is a broad-spectrum antifungal agent working as an iron chelator .
In vitro

Ciclopirox olamine (CPX) is a lipophilic bidentate iron chelator that stabilizes HIF-1alpha under normoxic conditions at lower concentrations than other iron chelators, probably by inhibiting HIF-1alpha hydroxylation. Ciclopirox olamine (CPX)-induced HIF-1 mediates reporter gene activity and endogenous HIF-1 target gene expression, including elevation of transcription, mRNA, and protein levels of the vascular endothelial growth factor (VEGF). Ciclopirox inhibits growth of C. albicans yeast and hyphal cells in a dose-dependent manner. Ciclopirox blocks H2O2-induced mitochondrial injury by maintaining mitochondrial transmembrane potential (Deltapsim). Ciclopirox completely blocks H2O2-stimulated release of lactate dehydrogenase (a marker of cell death) and decreases in MTT reduction (a marker of mitochondrial function) in adenocarcinoma SK-HEP-1 cells. Ciclopirox effectively inhibits H2O2-induced mitochondrial permeability transition pore (MPTP) opening. Ciclopirox increases the MTP, maintained it high, and blocks the ATP depletion in glucose-deprived SIN-1-treated astrocytes. Ciclopirox protects astrocytes from peroxynitritecytotoxicity by attenuating peroxynitrite-induced mitochondrial dysfunction. Ciclopirox is a substituted pyridone antimycotic drug, unrelated to the imidazole derivatives and its topical application ensures maximum local bioavailability. Ciclopirox acts on fungi by inhibiting the intracellular uptake of essential substrates and ions and this probably acts on the Candida ability to express its adherence mechanisms.

In vivo


Cell Data

cell lines:

Concentrations:

Incubation Time:

Powder Purity:≥99%

产品属性

ALogP 2

关联靶点(人)

PARP1 Tclin 聚[ADP-核糖]聚合酶1(Poly [ADP-ribose] polymerase 1) (0 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)

名称和识别符

Isomeric SMILES CC1=CC(=O)N(C(=C1)C2CCCCC2)O
分子量 207.27
Reaxy-Rn 1533423
Reaxys-RN link address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1533423&ln=

化学和物理性质

溶解性 Solubility (25°C) In vitro DMSO: 2 mg/mL (3.09 mM); Water: Insoluble; Ethanol: Insoluble;

安全和危险性(GHS)

象形图 GHS07
信号词 Warning
危险声明

H319: 引起严重眼睛刺激

H302: 吞食有害

H312: 皮肤接触有害

H332: 吸入有害

预防措施声明

P261: 避免吸入灰尘/烟雾/气体/雾/蒸汽/喷雾

P305+P351+P338: 如进入眼睛:用水小心冲洗几分钟。如戴隐形眼镜并可方便地取出,取出隐形眼镜。继续冲洗。

P280: 戴防护手套/穿防护服/戴防护眼罩/戴防护面具。

P302+P352: 如皮肤沾染:用水充分清洗。

P321: 特殊处理(请参阅此标签上的...)。

P501: 将内容物/容器处理到。。。

P264: 处理后要彻底洗手。

P271: 仅在室外或通风良好的地方使用。

P270: 使用本产品时,请勿进食、饮水或吸烟。

P304+P340: 如误吸入:将人转移到空气新鲜处,保持呼吸舒适体位。

P362+P364: 脱掉沾污的衣服,清洗后方可重新使用。

P330: 漱口

P264+P265: 处理后彻底洗手[和…]。不要触摸眼睛。

P301+P317: 如果被吞咽:请寻求医疗帮助。

P317: 寻求紧急医疗救助。

P337+P317: 如果眼睛刺激持续:寻求医疗帮助。

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:

溶液计算器