阿齐达芬尼科尔是一种半合成的氯霉素,其中的硝基部分被甲基砜取代,二氯乙酰胺被叠氮基乙酰胺取代,该化合物于1959年在拜耳公司首先合成。阿达芬尼醇通过与50S核糖体的23S亚基结合而起作用,从而抑制蛋白质的合成。阿齐达芬尼醇几乎没有受到研究关注,仅引用了少量文献。 Azidamfenicol is a semi-synthetic chloramphenicol in which the nitro moiety is replaced with a methylsulphone and the dichloroacetamide is replaced with azidoacetamide, first synthesised at Bayer in 1959. Azidamfenicol is a broad spectrum antibiotic with good activity against Gram negative and anaerobic bacteria. Azidamfenicol acts by binding to the 23S sub-unit of the 50S ribosome, inhibiting protein synthesis. Azidamfenicol has received little research attention with only a few literature citations.
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Azidamfenicol
Dangerous GoodsCAS number:13838-08-9 molecular formula:C11H13N5O5
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Specs
| Chinese alias | - | ||
| English alias | Berlicetin | threo-2-Azido-N-(beta-hydroxy-alpha-(hydroxymethyl)-p-nitrophenethyl)acetamide | Azidanfenicol [INN-Spanish] | Acetamide, 2-azido-N-((1R,2R)-2-hydroxy-1-(hydroxymethyl)-2-(4-nitrophenyl)ethyl)- | Acetamide, 2-azido-N-(2-hydroxy-1-(hydroxymeth | ||
| CAS number | 13838-08-9 | molecular formula | C11H13N5O5 |
| molecular weight | 295.25 g/mol | Exact mass | - |
| PSA | 130.000 Ų | logp | 1.000 |
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Safety information
pictogram:
GHS07
Signal word:
Warning
Hazard Statement:
H302: 吞食有害
Statement of Preventive Measures:
P501: 将内容物/容器处理到。。。 P264: 处理后要彻底洗手。 P270: 使用本产品时,请勿进食、饮水或吸烟。 P330: 漱口 P301+P317: 如果被吞咽:请寻求医疗帮助。
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