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Merck

SML2011

Sigma-Aldrich

环吡酮

≥98% (HPLC)

别名:

环吡酮胺, 6-环己基-1-羟基-4-甲基-2(1H)-吡啶酮, HOE 296b, 6-环己基-1-羟基-4-甲基-2(1H)-吡啶酮

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About This Item

经验公式(希尔记法):
C12H17NO2
CAS号:
分子量:
207.27
MDL號碼:
分類程式碼代碼:
12352200
NACRES:
NA.77

化驗

≥98% (HPLC)

形狀

powder

顏色

white to beige

溶解度

DMSO: 2 mg/mL, clear

運輸包裝

ambient

儲存溫度

2-8°C

SMILES 字串

ON1C(C2CCCCC2)=CC(C)=CC1=O

InChI

1S/C12H17NO2/c1-9-7-11(13(15)12(14)8-9)10-5-3-2-4-6-10/h7-8,10,15H,2-6H2,1H3

InChI 密鑰

SCKYRAXSEDYPSA-UHFFFAOYSA-N

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生化/生理作用

环吡酮是一种抗真菌和细胞可透过性的铁螯合剂。 研究发现它抑制多种酶和信号通路,包括脯氨酰羟化酶 2(PHD2)、真核翻译起始因子 5A(eIF5A)、Wnt/β-连环蛋白、低氧诱导因子-1α(HIF-1 α)/血管内皮生长因子( VEGF)、血管内皮生长因子受体 3(VEGFR-3)、雷帕霉素的哺乳动物靶标(mTOR)和细胞周期蛋白依赖性激酶(CDK)。 环吡酮除具有抗真菌活性外,还具有抗病毒和抗癌活性。 研究还表明,环吡酮以 p21 依赖性方式抵消糖尿病小鼠的糖毒性。
环吡酮是属于羟基吡啶酮类的化合物。研究发现它对皮肤癣菌、酵母、霉菌、某些细菌以及耐唑类念珠菌具有活性。与其他可抑制麦角固醇的抗真菌药不同,环吡酮具有不同的作用。它靶向降解真菌细胞过氧化物的金属依赖性酶。环吡酮的这种独特作用使得在病原真菌中抗药性几率较低。这种化合物用于指甲和皮肤特异性的局部配方。

象形圖

Exclamation mark

訊號詞

Warning

危險分類

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3


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