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docetaxel

中文名称
——
中文别名
——
英文名称
docetaxel
英文别名
paclitaxel;docataxel;docetaxol;taxotere;(1S,2S,4S,7R,9S,10S,12R,15S)-4-(acetyloxy)-15-{[(2R,3S)-3-{[(tert-butoxy)(hydroxy)methylidene]amino}-2-hydroxy-3-phenylpropanoyl]oxy}-1,9,12-trihydroxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.0^{3,10}.0^{4,7}]heptadec-13-en-2-yl benzoate;[(1S,2S,4S,7R,9S,10S,12R,15S)-4-acetyloxy-1,9,12-trihydroxy-15-[(2R,3S)-2-hydroxy-3-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoyl]oxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-2-yl] benzoate
docetaxel化学式
CAS
——
化学式
C43H53NO14
mdl
——
分子量
807.892
InChiKey
ZDZOTLJHXYCWBA-JXHJHTFNSA-N
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):
    1.6
  • 重原子数:
    58
  • 可旋转键数:
    13
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    224
  • 氢给体数:
    5
  • 氢受体数:
    14

反应信息

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文献信息

  • [EN] TARGETED THERAPEUTICS<br/>[FR] THÉRAPEUTIQUE CIBLÉE
    申请人:SYNTA PHARMACEUTICALS CORP
    公开号:WO2015038649A1
    公开(公告)日:2015-03-19
    The present invention provides pharmacological compounds including an effector moiety conjugated to a binding moiety that directs the effector moiety to a biological target of interest. Likewise, the present invention provides compositions, kits, and methods (e.g., therapeutic, diagnostic, and imaging) including the compounds. The compounds can be described as a protein interacting binding moiety-drug conjugate (SDC-TRAP) compounds, which include a protein interacting binding moiety and an effector moiety. For example, in certain embodiments directed to treating cancer, the SDC-TRAP can include an Hsp90 inhibitor conjugated to a cytotoxic agent as the effector moiety.
    本发明提供了包括与将效应子导向至感兴趣的生物靶点的结合基团共轭的药理化合物。同样,本发明提供了包括这些化合物的组合物、试剂盒和方法(例如治疗、诊断和成像)。这些化合物可以被描述为蛋白质相互作用结合基团-药物共轭(SDC-TRAP)化合物,其中包括蛋白质相互作用结合基团和效应子。例如,在针对治疗癌症的某些实施方式中,SDC-TRAP可以包括Hsp90抑制剂共轭到细胞毒性药剂作为效应子。
  • [EN] METHODS OF TREATING A SUBJECT AND RELATED PARTICLES, POLYMERS AND COMPOSITIONS<br/>[FR] MÉTHODES DE TRAITEMENT D'UN SUJET ET PARTICULES, POLYMÈRES ET COMPOSITIONS À CET EFFET
    申请人:FETZER OLIVER S
    公开号:WO2012044832A1
    公开(公告)日:2012-04-05
    Described herein are methods for treating a subject with combinations of polymer-agent particles and cyclodextrin polymer agent conjugates. The methods herein may be used to treat subjects identified with cancer, cardiovascular disorders, autoimmune disorders, or inflammatory disorders. Also described herein are compositions, dosage forms, and kits comprising polymer-agent particles and cyclodextrin polymer agent conjugates.
    本文描述了一种利用聚合物-药剂颗粒和环糊精聚合物药剂共轭物组合治疗受试者的方法。本文中的方法可用于治疗被诊断患有癌症、心血管疾病、自身免疫性疾病或炎症性疾病的受试者。本文还描述了包含聚合物-药剂颗粒和环糊精聚合物药剂共轭物的组合物、剂型和配套工具。
  • PROCESS FOR THE PREPARATION OF DOCETAXEL, ITS INTERMEDIATES, AND METHODS FOR PREPARATION THEREOF
    申请人:Shen Xin
    公开号:US20100311991A1
    公开(公告)日:2010-12-09
    The present invention disclosed an process for preparing docetaxel 1, including the following steps: a) hydroxyl acylation reaction of compound 2 and 3 to obtain compound 4; b) deprotection group R 1 of the hydroxyl group of compound 4 obtained from step a to prepare compound 5; c) removing one tert-butoxycarbonyl of compound 5 obtained from step b to prepare compound 6; d) removing one acetyl of compound 6 obtained from step c to prepare compound 1; wherein, R 1 represents tert-butyl dimethyl silyl, triethylsilyl, ethoxyethyl, tetrahydropyranyl, trichloroethoxycarbonyl or methoxymethyl, Boc is tert-butoxycarbonyl, Ac is acetyl, and Ph is phenyl. The present invention also disclosed intermediates of docetaxel and methods for preparation thereof. In the methods for preparation of the present invention, the protective groups used are easy to be removed, the purification of the intermediates is easy, the cost is lower, the yield and the purity are higher, and the processes can be scaled to commercial implementation.
    本发明揭示了一种制备紫杉醇1的方法,包括以下步骤:a)将化合物2和3进行羟基酰化反应以获得化合物4;b)去保护羟基群R1,其中R1代表叔丁基二甲基硅基、三乙基硅基、乙氧基乙基、四氢吡喃基、三氯乙氧羰基或甲氧基甲基,得到步骤a中获得的化合物4以制备化合物5;c)去除化合物5中从步骤b获得的一个叔丁氧羰基以制备化合物6;d)去除从步骤c获得的化合物6中的一个乙酰基以制备化合物1;其中,Boc代表叔丁氧羰基,Ac代表乙酰基,Ph代表苯基。本发明还揭示了紫杉醇的中间体及其制备方法。在本发明的制备方法中,所使用的保护基易于去除,中间体的纯化容易,成本较低,产率和纯度较高,并且这些过程可以扩展到商业实施。
  • POLYMER-AGENT CONJUGATES, PARTICLES, COMPOSITIONS, AND RELATED METHODS OF USE
    申请人:Eliasof Scott
    公开号:US20100247668A1
    公开(公告)日:2010-09-30
    Described herein are polymer-agent conjugates and particles, which can be used, for example, in the treatment of cancer. Also described herein are mixtures, compositions and dosage forms containing the particles, methods of using the particles (e.g., to treat a disorder), kits including the polymer-agent conjugates and particles, methods of making the polymer-agent conjugates and particles, methods of storing the particles and methods of analyzing the particles.
    本文描述了聚合物-药剂共轭物和颗粒,例如可用于癌症治疗。本文还描述了含有这些颗粒的混合物、组合物和剂型,使用这些颗粒的方法(例如治疗疾病),包括聚合物-药剂共轭物和颗粒的试剂盒,制备聚合物-药剂共轭物和颗粒的方法,存储颗粒的方法以及分析颗粒的方法。
  • [EN] NANOPARTICLE FORMULATIONS AND USES THEROF<br/>[FR] FORMULATIONS DE NANOPARTICULES ET LEURS UTILISATIONS
    申请人:ABRAXIS BIOSCIENCE LLC
    公开号:WO2010118365A1
    公开(公告)日:2010-10-14
    The present invention provides compositions comprising nanoparticles comprising: 1) a drug, such as a hydrophobic drug derivative; and 2) a carrier protein. Also provided are methods of treating diseases (such as cancer) using the compositions, as well as kits and unit dosages.
    本发明提供了包含纳米粒子的组合物,其中包括:1)药物,如疏水性药物衍生物;和2)载体蛋白。还提供了使用这些组合物治疗疾病(如癌症)的方法,以及套件和单元剂量。
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