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2-Amino-4-chloropyrimidine-5-carboxylic acid | 1240594-92-6

中文名称
——
中文别名
——
英文名称
2-Amino-4-chloropyrimidine-5-carboxylic acid
英文别名
2-amino-4-chloropyrimidine-5-carboxylic acid
2-Amino-4-chloropyrimidine-5-carboxylic acid化学式
CAS
1240594-92-6
化学式
C5H4ClN3O2
mdl
——
分子量
173.56
InChiKey
YISUXFZYHBEMSR-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):
    0.3
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    89.1
  • 氢给体数:
    2
  • 氢受体数:
    5

文献信息

  • [EN] 18F-LABELLED FOLATE/ANTIFOLATE ANALOGUES<br/>[FR] ANALOGUES DE FOLATES/ANTIFOLATES MARQUÉS AU 18F
    申请人:MERCK & CIE
    公开号:WO2013167653A1
    公开(公告)日:2013-11-14
    The present invention is directed towards new 18 F- folate/antifolate analogue radiopharmaceuticals, wherein the phenyl group within folate structures has been replaced by an 18F- heterocycle, their precursors, a method of their preparation, as well as their use in diagnosis of a cell or population of cells expressing a folate-receptor and monitoring of cancer and inflammatory and autoimmune diseases and therapy thereof.
    本发明涉及新的18F-叶酸/抗叶酸类似物放射性药物,其中叶酸结构中的苯基已被18F-杂环取代,其前体物,其制备方法,以及它们在诊断表达叶酸受体的细胞或细胞群以及癌症和炎症性和自身免疫疾病的监测和治疗中的应用。
  • HETEROCYCLIC COMPOUNDS AND USES THEREOF
    申请人:Castro Alfredo C.
    公开号:US20130029982A1
    公开(公告)日:2013-01-31
    Compounds and pharmaceutical compositions that modulate kinase activity, including PI3 kinase activity, and compounds, pharmaceutical compositions, and methods of treatment of diseases and conditions associated with kinase activity, including PI3 kinase activity, are described herein.
    本文描述了调节激酶活性(包括PI3激酶活性)的化合物和药物组合物,以及治疗与激酶活性(包括PI3激酶活性)相关的疾病和病情的化合物、药物组合物和治疗方法。
  • 18F-LABELLED FOLATE/ANTIFOLATE ANALOGUES
    申请人:MERCK & CIE
    公开号:US20150125390A1
    公开(公告)日:2015-05-07
    The present invention is directed towards new 18 F-folate/antifolate analogue radiopharmaceuticals, wherein the phenyl group within folate structures has been replaced by an 18 F-heterocycle, their precursors, a method of their preparation, as well as their use in diagnosis of a cell or population of cells expressing a folate-receptor and monitoring of cancer and inflammatory and autoimmune diseases and therapy thereof.
    本发明涉及新的18F-叶酸类/抗叶酸类模拟放射性药物,其中叶酸结构中的苯基已被18F-杂环取代,其前体,其制备方法,以及它们在诊断表达叶酸受体的细胞或细胞群以及癌症和炎症性和自身免疫疾病的监测和治疗中的应用。
  • 18F-labelled folate/antifolate analogues
    申请人:MERCK & CIE
    公开号:US10357576B2
    公开(公告)日:2019-07-23
    The present invention is directed towards new 18F-folate/antifolate analog radiopharmaceuticals, wherein the phenyl group within folate structures has been replaced by an 18F-heterocycle, their precursors, a method of their preparation, as well as their use in diagnosis of a cell or population of cells expressing a folate-receptor and monitoring of cancer and inflammatory and autoimmune diseases and therapy thereof.
    本发明涉及新型 18F 叶酸/抗叶酸类似放射性药物(其中叶酸结构中的苯基已被 18F 异环取代)、其前体、制备方法,以及它们在诊断表达叶酸受体的细胞或细胞群、监测癌症、炎症和自身免疫性疾病及其治疗中的用途。
  • MK2 INHIBITORS AND USES THEREOF
    申请人:Celgene CAR LLC
    公开号:US20210053984A1
    公开(公告)日:2021-02-25
    The present invention provides compounds, compositions thereof, and methods of using the same.
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