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- palonosetron hydroehloride 盐酸帕洛诺司琼
- OBJECTIVE To synthesize palonosetron hydrochloride. 目的合成盐酸帕洛诺司琼。
- Results: The total yield of palonosetron was 7.6%. 结果:合成了帕洛诺司琼;总收率7.;6%25。
- RESULTS The total yield of palonosetron hydrochloride was 76%. 结果合成了盐酸帕洛诺司琼,总收率76%25。
- Objective: To synthesize palonosetron a novel 5-HT3 receptar antegonist. 目的:合成新型5-HT3受体阻滞剂帕洛诺司琼。
- CONCLUSION The easily manipulated and reliable procedure to synthesize palonosetron hydrochloride is applicable. 结论本实验合成盐酸帕洛诺司琼,操作简便,提高了收率,缩短了反应时间。
- Our main produce is Palonosetron Hcl ,tetra-O-beta- Ribofuranose,Fluvoxamine,Fenoldopam,Dolasetron,Zidovudine,Mitotane,Alendronate Sodium,Nebivolol. 目前我们的主要产品有:盐酸帕洛诺司琼,四乙酰核糖,齐夫多定,胸苷,氟伏沙明,非洛多泮,多拉司琼,米托坦,阿仑磷酸钠,奈比洛尔。
- It produces anti-epilepsy ingredients and medical intermediates, Phenytoinum Natricum, sodium valproate, Divalproex sodium, Palonosetron and the intermediates. 公司生产抗癫痫原料和医药中间体苯妥英钠;丙戊酸钠;双丙戊酸钠;帕洛诺司琼及其中间体.
- Methods: Palonosetron was prepared from 1-naphthalenecarboxylic acid and 4-carbethoxypiperidine via a series of steps such as amination,cyclization,hydrolysis,dehydration,reduction,etc. 方法:以1萘-甲酸和4哌-啶甲酸乙酯为原料经胺化、成环、水解、胺化、脱水、关环、还原等反应合成目标物。
- Ritodrine hydroehloride injection 盐酸利托君注射液
- Compound clorprenaline hydroehloride tablet 复方氯丙那林鱼腥草素钠片
- Compound moxifloxacin hydroehloride eye drops 复方盐酸莫西沙星滴眼液
- Papaverine hydroehloride and sodium injection 盐酸罂粟碱氯化钠注射液
- Metaeyeline hydroehloride tablets 盐酸美他环素片
- Sertraline hydroehloride tablets 盐酸舍曲林片
- palonosetron hydrochloride injection 盐酸帕洛诺司琼注射液
- Berberine hydroehloride liniment 盐酸小檗碱
- Palonosetron hydrochloride for injection 盐酸帕洛诺司琼
- bis- (2-ehloroethyl) amine hydroehloride 双-(2-氯乙基)胺盐酸盐