1)  (R)-carbonyl reductase
					
	
					
				
				
	
					
				(R)-羰基还原酶
				1.
					Improved expression and catalytic efficiency of (R)-carbonyl reductase in Escherichia coli by secondary structure optimization of mRNA translation initiation region
						
						mRNA翻译起始区二级结构优化提高(R)-羰基还原酶的表达及催化效率
					
					2)  carbonyl reductase
					
	
					
				
				
	
					
				羰基还原酶
				1.
					Screening of strain producing carbonyl reductase and optimization of its fermentation conditions;
						
						4,4,4-三氟乙酰乙酸乙酯羰基还原酶产生菌的筛选及产酶条件研究
					2.
					Purification and characterization of a novel carbonyl reductase with high stereo-selectivity;
						
						一种新的高立体选择性羰基还原酶的性质及分离
					3.
					Cloning and Expression of Gene Encoding (R)-Specific Carbonyl Reductase from Candida Parapsilosis in Escherichia Coli;
						
						近平滑假丝酵母(Candida parapsilosis)(R)-专一性羰基还原酶基因的克隆与表达
					
					3)  activity of carbonyl reductase
					
	
					
				
				
	
					
				羰基还原酶活力
			
					5)  enantioselective reductase
					
	
					
				
				
	
					
				羰基不对称还原酶
				1.
					The carbonyl enantioselective reductase wa s purified with a combination of ammonium precipitation,Phenyl Superose hydroph obic chromatography,DEAE anion exchange,and native polyacrylamide gel electrop horesis.
						
						morganiiJ-8为出发菌株,菌体超声破碎后,经硫酸铵沉淀、Phenyl Superose疏水柱层析、DEAD阴离子柱层析和非变性凝胶电泳四步纯化获得电泳纯羰基不对称还原酶。
					
					6)  reductive carbonylation
					
	
					
				
				
	
					
				还原羰基化
				1.
					Effect of Promoters on PdCl_2-Phenanthroline Catalyzed Reductive Carbonylation of Nitrobenzene;
						
						还原羰基化Pd-Phen催化剂体系中Ce(SO_4)_2的助催作用
					2.
					Nitrobenzene and its derivatives can react with 2-aminopyridine as coreagent by using the method of selenium-catalyzed CO reductive carbonylation.
						
						采用硒催化的一氧化碳还原羰基化法 ,由硝基苯衍生物与 2 氨基吡啶进行反应 ,得到的不是比例相当的三种脲类物质混合物 ,而主要得到非对称的吡啶脲 。
					3.
					Selenium catalyzed reductive carbonylation of PhNO 2 in alcohol media was studied and a series of phenyl carbamate products were obtained.
						
						详细考察了醇介质 中硒催化的硝基苯还原羰基化生成苯氨 基甲酸酯的 反应,获得 了一系列苯氨基甲酸酯产物。
					补充资料:[3-(aminosulfonyl)-4-chloro-N-(2.3-dihydro-2-methyl-1H-indol-1-yl)benzamide]
		分子式:C16H16ClN3O3S
分子量:365.5
CAS号:26807-65-8
性质:暂无
制备方法:暂无
用途:用于轻、中度原发性高血压。
		
		分子量:365.5
CAS号:26807-65-8
性质:暂无
制备方法:暂无
用途:用于轻、中度原发性高血压。
说明:补充资料仅用于学习参考,请勿用于其它任何用途。
	参考词条