Cycloheximide

CAS : 66-81-9

Ref. TR-C988270

Informations sur le produit

• Nom: Cycloheximide
• Synonymes: 4-[(2R)-2-[(1S,3S,5S)-3,5-dimethyl-2-oxocyclohexyl]-2-hydroxyethyl]piperidine-2,6-dione, 2,6-Piperidinedione, 2,6-Piperidinedione, 4-[(2R)-2-[(1S,3S,5S)-3,5-dimethyl-2-oxocyclohexyl]-2-hydroxyethyl]-, 2,6-Piperidinedione, 4-[2-(3,5-dimethyl-2-oxocyclohexyl)-2-hydroxyethyl]-, [1S-[1α(S*),3α,5β]]-, 3-(2-(3,5-Dimethyl-2-Oxocyclohexyl)-2-Hydroxyethyl)Glutarimide, 3-[2-(3,5-Dimethyl-2-oxo-1-cyclohexyl)-2-hydroxyethyl]glutarimide, 4-(2-(3,5-Dimethyl-2-oxocyclohexyl)-2-hydroxyethyl), 4-[(2R)-2-[(1S,3S,5S)-3,5-Dimethyl-2-oxocyclohexyl]-2-hydroxyethyl]-2,6-piperidinedione, 4-[2-(3,5-Dimethyl-2-Oxocyclohexyl)-2-Hydroxyethyl]Piperidine-2,6-Dione, 4-{(2R)-2-[(1S,3S,5S)-3,5-dimethyl-2-oxocyclohexyl]-2-hydroxyethyl}piperidine-2,6-dione, Acti-Aid, Acti-dione, Acti-dione BR, Acti-dione PM, Acti-dione TGF, Actidion, Actidione, Cicloheximid, Cicloheximida, Cicloheximide, Cycloheximid, Ft 3422-2, Glutarimide, 3-[2-(3,5-dimethyl-2-oxocyclohexyl)-2-hydroxyethyl]-, Ldn 97549, Naramycin, Naramycin A, Naramycin Microcapsule D 80, Naramycin NM-MCU 80, Nm-Mcd 80, Nsc 185, TZA, U 4527, l-Cycloheximide, β-[2-(3,5-Dimethyl-2-oxocyclohexyl)-2-hydroxyethyl]glutarimide

Description

Applications Cycloheximide is an antibiotic substance isolated from the beers of streptomycin-producing strains of Streptomyces griseus. Cycloheximide is used as fungicide.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Whiffen, A.J., et al.: J. Bacterial., 56, 283 (1948), Monsalve, E., et al.: J. Immunol., 176, 5362 (2006), Yang, J., et al.: J. Clin. Invest. 120, 2563 (2010),

• Marque: TRC

Propriétés chimiques

• Masse moléculaire: 281.35
• Formule: C₁₅H₂₃NO₄
• Couleur/Forme: Neat
• InChI: 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
• Code InChI: InChIKey=YPHMISFOHDHNIV-FSZOTQKASA-N
• SMILES: C[C@H]1C[C@H](C)C(=O)[C@H]([C@H](O)CC2CC(=O)N=C(O)C2)C1