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2-Acetoxymethyl-imidazol | 45815-85-8

中文名称
——
中文别名
——
英文名称
2-Acetoxymethyl-imidazol
英文别名
1H-imidazol-2-ylmethyl acetate
2-Acetoxymethyl-imidazol化学式
CAS
45815-85-8
化学式
C6H8N2O2
mdl
MFCD19218240
分子量
140.142
InChiKey
VSURUMQJCQNVDO-UHFFFAOYSA-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):
    -0.2
  • 重原子数:
    10
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.333
  • 拓扑面积:
    55
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    参考文献:
    名称:
    Molecular structure of 3,4,5-trihydro-2-oxo-1,5-ethanobenzazepine and its reaction with .beta.-amino alcohols as a model for the acylation step of the serine proteases
    摘要:
    DOI:
    10.1021/jo00375a020
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文献信息

  • Method of treating cancer
    申请人:——
    公开号:US20030220241A1
    公开(公告)日:2003-11-27
    The present invention relates to methods of treating cancer using a combination of a compound which is a PSA conjugate and a compound which is a inhibitor of prenyl-protein transferase, which methods comprise administering to said mammal, either sequentially in any order or simultaneously, amounts of at least two therapeutic agents selected from a group consisting of a compound which is a PSA conjugate and a compound which is a inhibitor of prenyl-protein transferase. The invention also relates to methods of preparing such compositions.
    本发明涉及使用一种PSA共轭物和一种前脂蛋白转移酶抑制剂的组合治疗癌症的方法,该方法包括向所述哺乳动物施用来自以下组中选择的至少两种治疗剂的量,所述组包括一种PSA共轭物和一种前脂蛋白转移酶抑制剂,所述治疗剂可以顺序给药或同时给药。该发明还涉及制备这种组合物的方法。
  • HYBRID BLOCK COPOLYMER MICELLES WITH MIXED STEREOCHEMISTRY FOR ENCAPSULATION OF HYDROPHOBIC AGENTS
    申请人:SILL Kevin N.
    公开号:US20080274173A1
    公开(公告)日:2008-11-06
    The present invention relates to the field of polymer chemistry and more particularly to multiblock copolymers and micelles comprising the same.
    本发明涉及聚合物化学领域,更具体地说是涉及多嵌段共聚物以及包含该共聚物的胶束。
  • Inhibitors of prenyl-protein transferase
    申请人:——
    公开号:US20020010184A1
    公开(公告)日:2002-01-24
    The present invention comprises piperazinone-containing compounds which inhibit prenyl-protein transferases, including famesyl-protein transferase and geranylgeranyl-protein transferase type I. Such therapeutic compounds are useful in the treatment of cancer.
    该发明涉及含有哌嗪酮类化合物,可抑制前列蛋白转移酶,包括法美基蛋白转移酶和戈楞基蛋白转移酶I型。这种治疗性化合物对癌症的治疗具有用处。
  • [EN] A METHOD OF TREATING CANCER<br/>[FR] UNE METHODE POUR LE TRAITEMENT DU CANCER
    申请人:MERCK & CO INC
    公开号:WO2000059930A1
    公开(公告)日:2000-10-12
    The present invention relates to methods of treating cancer using a combination of a compound which is a PSA conjugate and a compound which is an inhibitor of prenyl-protein transferase, which methods comprise administering to said mammal, either sequentially in any order or simultaneously, amounts of at least two therapeutic agents selected from a group consisting of a compound which is a PSA conjugate and a compound which is an inhibitor of prenyl-protein transferase. The invention also relates to methods of preparing such compositions.
    本发明涉及使用一种PSA共轭物和一种前尼基蛋白转移酶抑制剂的组合治疗癌症的方法,该方法包括向哺乳动物施用至少两种治疗剂量,所述治疗剂量从以下组合中选择:一种是PSA共轭物,一种是前尼基蛋白转移酶抑制剂,无论是按顺序或同时施用。本发明还涉及制备这种组合物的方法。
  • [EN] INHIBITORS OF PRENYL-PROTEIN TRANSFERASE<br/>[FR] INHIBITEURS DE PRENYL-PROTEINE-TRANSFERASES
    申请人:MERCK & CO., INC.
    公开号:WO1999009985A1
    公开(公告)日:1999-03-04
    (EN) The present invention is directed to compounds which inhibit prenyl-protein transferases, farnesyl-protein transferase and geranylgeranyl-protein transferase type I, and the prenylation of the oncogene protein Ras. The invention is further directed to chemotherapeutic compositions containing the compounds of this invention and methods for inhibiting farnesyl-protein transferase and geranylgeranyl-protein transferase type I and the prenylation of the oncogene protein RAS.(FR) L'invention concerne des composés qui inhibent les prényl-protéine-transférases, la farnésyl-protéine-transférase et la géranylgéranyl-protéine-transférase de type I, de même que la prénylation de la protéine oncogène Ras. L'invention concerne également des compositions chimiothérapeutiques renfermant les composés considérés, ainsi que des procédés permettant d'inhiber la farnésyl-protéine-transférase, la géranylgéranyl-protéine-transférase de type I et la prénylation de la protéine oncogène Ras.
    该发明涉及抑制异戊二烯基-蛋白质转移酶、法尼基-蛋白质转移酶和生长酰基-蛋白质转移酶I型以及癌基因蛋白Ras的异戊二烯基化的化合物。该发明还涉及含有该发明化合物的化疗组合物以及抑制法尼基-蛋白质转移酶、生长酰基-蛋白质转移酶I型和癌基因蛋白Ras的异戊二烯基化的方法。
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