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1)  validamine
井冈霉胺
1.
In our lab, validamycins were used as raw material, cyclitol compounds such as vaienamine, validamine, and validoxylamine A were obtained by microbial catalysis.
本实验室以井冈霉素为原料,采用微生物催化技术,得到了环醇类物质井冈胺、井冈霉胺和井冈霉亚基胺A。
2)  valiolamine
井冈霉醇胺
1.
N-Substituted chemical modification of valiolamine,as well as the inhibitory activity of these compounds against porcine and rat intestinal maltase and surase are discussed in detail.
井冈霉醇胺、井冈霉胺和井冈胺等假氨基糖类物质是新型的α 糖苷酶抑制剂,对其进行化学修饰可以得到糖苷酶抑制活性更强的N 取代假氨基糖衍生物。
3)  Valienamine
井冈霉烯胺
4)  validoxylamine A
井冈霉亚基胺A
1.
The product of valG gene was involved in transferring β-D glucose to validoxylamine A to produce validamycin A.
jinganggensis)DX546中,将负责井冈霉素A生物合成最后一步糖基转移中的糖基转移酶基因valG置换突变,多聚酶链式反应结果显示valG被阿泊拉霉素抗性基因成功置换,通过高压液相色谱检测证实突变株的发酵产物中井冈霉亚基胺A的产量得到大幅提高。
2.
In our lab, validamycins were used as raw material, cyclitol compounds such as vaienamine, validamine, and validoxylamine A were obtained by microbial catalysis.
本实验室以井冈霉素为原料,采用微生物催化技术,得到了环醇类物质井冈胺、井冈霉胺和井冈霉亚基胺A。
5)  validoxylamine
井冈霉亚基胺
1.
Validamycins have been one of the most popular and economical biopesticides in China, by microbial transformation of which validoxylamine A and valienamine can be produced.
井冈霉素目前已成为我国最经济最受欢迎的生物农药之一,用微生物转化法分解井冈霉素可以得到井冈霉亚基胺A和井冈胺,前者对海藻糖酶有强烈的抑制作用,有望开发成为新型生物杀虫剂,而后者是一种糖苷酶抑制剂,也可作为合成降糖药的原料。
6)  tetra-O-benzylvalienamine
2,3,4,6-四-O-苄基井冈霉烯胺
1.
Synthesis of tetra-O-benzylvalienamine
2,3,4,6-四-O-苄基井冈霉烯胺的合成
补充资料:井冈霉烯胺
分子式:C7H13NO4
分子量:175.18
CAS号:38231-86-6

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