Cycloheximide, =94%

Key Features and Details

Cycloheximide

SYNONYMS: Acti-Dione; 3-[2-(3,5-Dimethyl-2-oxocyclohexyl)-2-hydroxyethyl] glutarimide; Naramycin A; Actidione
CAS: # 66-81-9
MOLECULAR FORMULA: C15H23NO4
MOLECULAR WEIGHT: 281.352 g/mol
BEILSTEIN REGISTRY No.: 88868
EC No: 200-636-0
MDL No: MFCD00082346
SKU 02100183-CF Categories , , Tag

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PRODUCT DESCRIPTION

Cycloheximide Application Notes Cycloheximide is used in protein synthesis in apoptosis. It is also used in plant research to study disease resistance and as an ethylene stimulant, useful in studies involving fruit and leaf production. Usage Statement Unless specified otherwise, MP Biomedical's products are for research or further manufacturing use only, not for direct human use. For more information, please contact our customer service department. Key Applications Gene expression | steroidogenesis Studies | Disease resistance Studies
SPECIFICATIONS
SKU: 02100183-CF
Base Catalog Number: 100183
Alternate Names: Acti-Dione; 3-[2-(3,5-Dimethyl-2-oxocyclohexyl)-2-hydroxyethyl] glutarimide; Naramycin A; Actidione
Beilstein Registration No : 88868
Biochemical Physiological Actions : Cycloheximide (CHX) is an antibiotic produced by S. griseus. Its main biological activity is translation inhibition in eukaryotes resulting in cell growth arrest and cell death. CHX is widely used for selection of CHX-resistant strains of yeast and fungi, controlled inhibition of protein synthesis for detection of short-lived proteins and super-induction of protein expression, and apoptosis induction or facilitation of apoptosis induction by death receptors.
CAS : # 66-81-9
EC No : 200-636-0
Format : Powder
Hazard Statements : H300-H341-H360D
MDL No : MFCD00082346
Melting Point : 247 to 250° F (EPA, 1998)
Molecular Formula : C15H23NO4
Molecular Weight : 281.352 g/mol
PPE : Eyeshields, Faceshields, full-face particle respirator type , Gloves, respirator cartridge, respirator filter, respirator cartridges
Purity : =94%
RTECS No : MA4375000
Safety Symbol : GHS06, GHS08
Solubility : 10 to 50 mg/mL at 68° F (NTP, 1992)
Source : Microbial

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