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C1988

Sigma-Aldrich

环己酰亚胺,大包装

Biotechnology Performance Certified

同義詞:

3- [2-(3,5-二甲基-2-氧代环己基)-2-羟乙基]戊二酰亚胺, 放线菌酮, 纳拉霉素A

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About This Item

經驗公式(希爾表示法):
C15H23NO4
CAS號碼:
分子量::
281.35
Beilstein:
88868
EC號碼:
MDL號碼:
分類程式碼代碼:
51102829
PubChem物質ID:
NACRES:
NA.85

等級

Biotechnology Performance Certified

形狀

powder

技術

cell culture | mammalian: suitable

雜質

endotoxin, tested

溶解度

ethanol: 50 mg/mL

抗生素活性譜

fungi
yeast

作用方式

protein synthesis | interferes

儲存溫度

2-8°C

SMILES 字串

[H][C@]1(C[C@@H](C)C[C@H](C)C1=O)[C@H](O)CC2CC(=O)NC(=O)C2

InChI

1S/C15H23NO4/c1-8-3-9(2)15(20)11(4-8)12(17)5-10-6-13(18)16-14(19)7-10/h8-12,17H,3-7H2,1-2H3,(H,16,18,19)/t8-,9-,11-,12+/m0/s1

InChI 密鑰

YPHMISFOHDHNIV-FSZOTQKASA-N

基因資訊

尋找類似的產品? 前往 產品比較指南

相關類別

應用

环己酰亚胺被广泛用于筛选抗 CHX 的酵母和真菌菌株,控制蛋白合成的抑制作用(用于检测短寿蛋白和蛋白表达的超诱导作用),并诱导细胞凋亡或通过死亡受体促进细胞凋亡。研究表明,它可以选择性清除动脉粥样硬化斑块中的巨噬细胞并激活无积聚的马卵母细胞。

生化/生理作用

作用机制:真核生物中的翻译抑制导致细胞生长停滞和细胞死亡。CHX被广泛用于抗CHX的酵母和真菌菌株的选择、蛋白质合成的受控抑制以检测短寿命蛋白质和蛋白质表达的超诱导作用、以及诱导凋亡或促进通过死亡受体诱导的凋亡。

活性谱:具有抑制酵母和真菌如念珠菌、曲霉、酵母菌和青霉的活性
环己酰亚胺(CHX)是灰色链霉菌产生的一种抗生素,可抑制真核生物中的蛋白质生物合成。它使参与肽链延伸的转移酶 II 失活。最近的研究表明,CHX 结合 60S 核糖体,并特异性地阻止了延伸过程中的易位步骤。

訊號詞

Danger

危險分類

Acute Tox. 2 Oral - Aquatic Chronic 2 - Muta. 2 - Repr. 1B

儲存類別代碼

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


分析證明 (COA)

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Valerie Croons et al.
The Journal of pharmacology and experimental therapeutics, 320(3), 986-993 (2006-12-01)
Macrophages are an essential component of unstable atherosclerotic plaques and play a pivotal role in the destabilization process. We have demonstrated previously that local delivery of the mammalian target of rapamycin (mTOR) inhibitor everolimus selectively clears macrophages in rabbit plaques.
Mechanism of cycloheximide inhibition of protein synthesis in a cell-free system prepared from rat liver.
B S Baliga et al.
The Journal of biological chemistry, 244(16), 4480-4489 (1969-08-25)
Tilman Schneider-Poetsch et al.
Nature chemical biology, 6(3), 209-217 (2010-02-02)
Although the protein synthesis inhibitor cycloheximide (CHX) has been known for decades, its precise mechanism of action remains incompletely understood. The glutarimide portion of CHX is seen in a family of structurally related natural products including migrastatin, isomigrastatin and lactimidomycin
Y H Choi et al.
Reproduction (Cambridge, England), 122(1), 177-183 (2001-06-27)
Two different culture media (TCM-199 and follicular fluid), two activation treatments (10 and 50 micromol calcium ionophore l(-1)) and three culture periods with cycloheximide were evaluated to find effective culture conditions for activation of cumulus-free equine oocytes. Oocytes were collected
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我們的科學家團隊在所有研究領域都有豐富的經驗,包括生命科學、材料科學、化學合成、色譜、分析等.

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