CAS 7384-89-6
:L-eritro-Cloramfenicolo
- 2,2-Dichloro-N-[(1S,2R)-2-hydroxy-1-(hydroxymethyl)-2-(4-nitrophenyl)ethyl]acetamide
- <span class="text-smallcaps">L</span>-(+)-erythro-Chloramphenicol
- <span class="text-smallcaps">L</span>-erythro-(1R,2S)-1-p-Nitrophenyl-2-dichloroacetamido-1,3-propanediol
- <span class="text-smallcaps">L</span>-erythro-2,2-Dichloro-N-[β-hydroxy-α-(hydroxymethyl)-p-nitrophenethyl]acetamide
- Acetamide, 2,2-dichloro-N-[b-hydroxy-a-(hydroxymethyl)-p-nitrophenethyl]-, L-erythro-(+)- (8CI)
- Acetamide, 2,2-dichloro-N-[β-hydroxy-α-(hydroxymethyl)-p-nitrophenethyl]-, <span class="text-smallcaps">L</span>-erythro-(+)-
- Acetamide,2,2-dichloro-N-[2-hydroxy-1-(hydroxymethyl)-2-(4-nitrophenyl)ethyl]-,[R-(R*,S*)]-
- L-(+)-erythro-Chloramphenicol
- L-erythro-(1R,2S)-1-p-Nitrophenyl-2-dichloroacetamido-1,3-propanediol
- L-erythro-2,2-Dichloro-N-[b-hydroxy-a-(hydroxymethyl)-p-nitrophenethyl]acetamide
- Acetamide, 2,2-dichloro-N-[β-hydroxy-α-(hydroxymethyl)-p-nitrophenethyl]-, L-erythro-(+)-
- Acetamide, 2,2-dichloro-N-[(1S,2R)-2-hydroxy-1-(hydroxymethyl)-2-(4-nitrophenyl)ethyl]-
- Chloramphenicol Impurity 21
- Vedi altri sinonimi
L-erythro-Chloramphenicol
CAS:Prodotto controllatoApplications L-erythro-Chloramphenicol functions as a potent inhibitor of electron transport in the mitochondria in biological studies. The L-isomer can be identified from the other CAP-isomers through reversed phase and chiral liquid chromatography in combination with tandem mass spectrometric detection.
References Berendsen, B., et al.: Anal. Chim. Acta., 700, 78 (2011), Wilson, S.B., et al.: Biochim. Biophys. Acta., 292, 603 (1973)Formula:C11H12Cl2N2O5Colore e forma:NeatPeso molecolare:323.13L-Erythro-chloramphenicol
CAS:L-Erythro-chloramphenicol is a deacylated form of chloramphenicol, which inhibits protein synthesis by binding to the bacterial ribosome. It is an antibiotic that is used to treat bacterial infections. L-Erythro-chloramphenicol has been shown to inhibit mitochondrial protein synthesis and mitochondrial proteins in mitochondria. The drug also inhibits the production of proteins in bacterial cells, such as extracts from Escherichia coli and escherichia coli. L-Erythro-chloramphenicol has two dichloroacetyl isomers, which are responsible for its antibacterial activity. The phenyl ring on the molecule serves as a site for chemical reactions with other molecules.
Formula:C11H12Cl2N2O5Purezza:Min. 95%Peso molecolare:323.13 g/molL-erythro-Chloramphenicol
CAS:L-erythro-Chloramphenicol functions as a potent inhibitor of electron transport.Formula:C11H12Cl2N2O5Purezza:98%Colore e forma:SolidPeso molecolare:323.13


