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Cycloheximide
品牌:AG Scientific
货号:
规格:1 g
货期:

CAS:66-81-9Formula:C15H23NO4MW:281.35Appearance:Whiteorcreamcolorpowder.Purity:95%

商品详情 参考文献 相关资料

Cycloheximide is an antibiotic active against many yeasts and fungi. Inhibits protein synthesis in eukaryotes (but not in prokaryotes) by interfering with the translocation step. It inhibits chain initiation as well as chain elongation by acting on the 60S subunit of the eukaryote ribosome, interacting directly with enzyme translocase. Cycloheximide is used as an inhibitor to study cell-free protein biosynthesis in eukaryotes and also used to block ribosome-dependent in vivo polypeptide synthesis. It induces apoptosis in a variety of cells, but can also delay or inhibit apoptosis by other agents.

Cycloheximide’s longstanding application as a gene selection antibiotic has a powerful new role in Genome editing utilizing the CRISPR/Cas9 systemA Candida albicans CRISPR system permits genetic engineering of essential genes and gene families.

Cycloheximide is in stock. Call for bulk quotations, typical lead for subdivision, packing and shipping larger quantities is 7-14 days.
Research size order 100mg 250mg lead is shorter.
International Shipping of this material can be subject to an additional hazardous shipping fee.

 

Additional Information

SynonymsActidione, Naramycin A, NSC-185, U-4527
Product #C-1189
CAS #66-81-9
Chemical Name4-[(2R)-2-[(1S,3S,5S)-3,5-DIMETHYL-2-OXOCYCLOHEXYL]-2-HYDROXYETHYL]PIPERIDINE-2,6-DIONE
FormulaC15H23NO4
MW281.35
AppearanceWhite or cream color powder.
Purity95%
SolubilitySoluble in Chloroform, Ethanol and Methanol.
PreparationStore solutions at -20°C
Storage TempStore desiccated at +4°C
Therapeutic AreaInfectious Diseases
UseCycloheximide is a highly effective antibiotic with activity against mold, yeast, and phytopathogenic fungi, with lower activity against bacteria

Additional Information

MDL NumberMFCD00082346
ChemACXX1006248-5
InChIInChI=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
SMILESC[C@H]1C[C@@H](C(=O)[C@@H](C1)[C@@H](CC2CC(=O)NC(=O)C2)O)C
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