C7698

Cycloheximide

from microbial, ≥94% (TLC)

Manufacturer: Sigma Aldrich

CAS Number: 66-81-9

Synonym(S): 3-[2-(3,5-Dimethyl-2-oxocyclohexyl)-2-hydroxyethyl]glutarimide, Actidione, Naramycin A

Select a Size

Pack Size SKU Availability Price
1 G C7698-1-G In Stock ₹ 10,770.88
5 G C7698-5-G In Stock ₹ 25,417.10

C7698 - 1 G

₹ 10,770.88

In Stock

Quantity

1

Base Price: ₹ 10,770.88

GST (18%): ₹ 1,938.758

Total Price: ₹ 12,709.638

biological source

microbial

Quality Level

200

Assay

≥94% (TLC)

form

powder

color

white to off-white

solubility

ethanol: soluble, clear to hazy

antibiotic activity spectrum

fungiyeast

Mode of action

protein synthesis | interferes

storage temp.

2-8°C

SMILES string

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

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Description

  • General description: Cycloheximide, also known as Actidione, is a glutarimide antibiotic commonly derived from the bacterium Streptomyces griseus. It acts as a potent inhibitor of protein biosynthesis in eukaryotic cells by disrupting the translocation step during translation, effectively blocking translational elongation. In microbiology, it plays a crucial role as a selection agent for resistant strains of yeast and fungi, proving invaluable in controlled experimental environments.In cell biology and biochemical research, Cycloheximide showcases a dual nature concerning Apoptosis Induction, inducing or inhibiting apoptosis depending on the cell type. Its rapid and reversible effects make it an ideal choice for studying cellular processes and determining protein half-life. Cycloheximide also finds extensive applications in biomedical research, where it inhibits protein synthesis in eukaryotic cells studied in vitro (outside of organisms) and its effects are rapidly reversed by simply removing it. This makes Cycloheximide a go-to choice for exploring cell biology, biomedical and biochemical research, offering precise control and versatility in experiments.
  • Application: In yeast strains, cycloheximide has been used as a protein synthesis inhibitor in the cycloheximide chase experiment.[1] It has been used to inhibit translation in mammalian cells.[2][3]It has been used to suppress fungal growth.[4]
  • Biochem/physiol Actions: Mode of Action: Translation inhibition in eukaryotes resulting in cell growth arrest and cell death. CHX is widely used for the 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. Activity Spectrum: Active against yeast and fungi like Candida, Aspergillus, Saccharomyces, Penicillium
  • Features and Benefits: High-quality antibiotic suitable for multiple research applicationsCommonly used in Cell Biology and Biochemical applications
  • Storage and Stability: Tightly closed. Dry. Keep in a well-ventilated place. Keep locked up or in an area accessible only to qualified or authorized persons.
  • Other Notes: For additional information on our range of Biochemicals, please complete this form.

SAFETY INFORMATION

Pictograms

GHS06,GHS08,GHS09

Signal Word

Danger

Hazard Statements

H300,H341,H360D,H411

Precautionary Statements

P202 - P264 - P273 - P280 - P301 + P310 - P391

Hazard Classifications

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves