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Calcium;(3R,5S)-7-[4-(4-fluorophenyl)-2-[methyl(methylsulfonyl)amino]-6-propan-2-ylpyrimidin-5-yl]-3,5-dihydroxyhept-6-enoate

中文名称
——
中文别名
——
英文名称
Calcium;(3R,5S)-7-[4-(4-fluorophenyl)-2-[methyl(methylsulfonyl)amino]-6-propan-2-ylpyrimidin-5-yl]-3,5-dihydroxyhept-6-enoate
英文别名
——
Calcium;(3R,5S)-7-[4-(4-fluorophenyl)-2-[methyl(methylsulfonyl)amino]-6-propan-2-ylpyrimidin-5-yl]-3,5-dihydroxyhept-6-enoate化学式
CAS
——
化学式
C44H54CaF2N6O12S2
mdl
——
分子量
1001.1
InChiKey
LALFOYNTGMUKGG-VKLRDTKISA-L
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    1.75
  • 重原子数:
    67
  • 可旋转键数:
    18
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    304
  • 氢给体数:
    4
  • 氢受体数:
    20

反应信息

  • 作为产物:
    描述:
    瑞舒伐他汀钠 以78的产率得到Calcium;(3R,5S)-7-[4-(4-fluorophenyl)-2-[methyl(methylsulfonyl)amino]-6-propan-2-ylpyrimidin-5-yl]-3,5-dihydroxyhept-6-enoate
    参考文献:
    名称:
    USRE37314E1
    摘要:
    公开号:
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文献信息

  • Methods for predicting the response to statins
    申请人:Murata Glen H.
    公开号:US20110245283A1
    公开(公告)日:2011-10-06
    The invention provides methods for optimizing therapeutic efficacy for treating hypercholesterolemia in a subject having a cardiovascular disease (CVD), comprising (a) determining subject characteristics that affect the likelihood of reaching a goal level of low density lipoprotein (LDL); and (b) obtaining success probabilities of a variety of statin treatments for reaching said goal level of LDL using said subject characteristics and a multivariate model; and (c) administrating the optimal statin treatment with the highest success probability of step (b) to said subject thereby optimizing therapeutic efficacy for treating hypercholesterolemia in said subject.
    该发明提供了一种优化治疗高胆固醇血症的方法,用于治疗患有心血管疾病(CVD)的受试者,包括(a)确定影响达到低密度脂蛋白(LDL)目标平可能性的受试者特征;和(b)利用受试者特征和多元模型获取各种他汀治疗达到所述LDL目标平的成功概率;以及(c)向该受试者施用步骤(b)中具有最高成功概率的最佳他汀治疗,从而优化治疗高胆固醇血症的治疗效果。
  • [EN] PROCESSES FOR THE PREPARATION OF ROSUVASTATIN OR PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF<br/>[FR] PROCÉDÉ DE PRÉPARATION DE ROSUVASTATINE OU DE SELS PHARMACEUTIQUEMENT ACCEPTABLES DE CELLE-CI
    申请人:LAURUS LABS PRIVATE LTD
    公开号:WO2016125086A1
    公开(公告)日:2016-08-11
    The present invention relates to processes for the preparation of rosuvastatin calcium of formula I and pharmaceutically acceptable salts thereof using novel intermediates, and to a pharmaceutical composition containing the same.
    本发明涉及制备式I的瑞舒伐他汀钙及其药学上可接受的盐的新型中间体的过程,以及含有该物质的药物组合物。
  • NOVEL METHOD FOR PREPARING ROSUVASTATIN, INTERMEDIATE COMPOUNDS USEFUL FOR PREPARING SAME, AND METHOD FOR PREPARING SAME
    申请人:Lee Hongwoo
    公开号:US20120136151A1
    公开(公告)日:2012-05-31
    The present invention relates to novel intermediate compounds used in preparing Rosuvastatin or the pharmaceutically acceptable salts thereof, to a method for preparing same, and to a method for preparing Rosuvastatin or the pharmaceutically acceptable salts thereof from the intermediates. The preparation method of the present invention has the effect of providing Rosuvastatin hemi-calcium salts with an excellent yield rate.
    本发明涉及用于制备Rosuvastatin或其药用盐的新型中间化合物,以及制备相同的方法,以及从这些中间体制备Rosuvastatin或其药用盐的方法。本发明的制备方法具有提供具有优异产率的Rosuvastatin半盐的效果。
  • [EN] ROSUVASTATIN INTERMEDIATES AND THEIR PREPARATION<br/>[FR] INTERMÉDIAIRES DE LA ROSUVASTATINE ET LEUR PRÉPARATION
    申请人:TEVA PHARMA
    公开号:WO2009009152A1
    公开(公告)日:2009-01-15
    Provided are processes and intermediates for preparation of rosuvastatin.
    提供了用于制备罗伐他汀的过程和中间体。
  • [EN] PROCESS FOR THE PREPARATION OF ROSUVASTATIN<br/>[FR] PROCÉDÉ DE PRÉPARATION DE ROSUVASTATINE
    申请人:KRKA TOVARNA ZDRAVIL D D NOVO
    公开号:WO2010081861A1
    公开(公告)日:2010-07-22
    The invention relates to a process for the preparation of a HMG - CoA reductase inhibitor such as rosuvastatin, as well as intermediates useful in such process. The invention also relates to salts of HMG-CoA reductase inhibitors and processes for preparing same as well as processes for preparing pharmaceutically acceptable salts of HMG-CoA reductase inhibitors.
    该发明涉及一种用于制备类似罗伐他汀HMG - CoA还原酶抑制剂的过程,以及在该过程中有用的中间体。该发明还涉及HMG-CoA还原酶抑制剂的盐以及制备其的过程,以及制备HMG-CoA还原酶抑制剂的药用可接受盐的过程。
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