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2-Amino-3-(2,3-dibromo-4-hydroxy-phenyl)propanoic acid

中文名称
——
中文别名
——
英文名称
2-Amino-3-(2,3-dibromo-4-hydroxy-phenyl)propanoic acid
英文别名
2-amino-3-(2,3-dibromo-4-hydroxyphenyl)propanoic acid
2-Amino-3-(2,3-dibromo-4-hydroxy-phenyl)propanoic acid化学式
CAS
——
化学式
C9H9Br2NO3
mdl
——
分子量
338.98
InChiKey
NKLMLRIOJDRBCZ-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):
    -0.4
  • 重原子数:
    15
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    83.6
  • 氢给体数:
    3
  • 氢受体数:
    4

文献信息

  • [EN] PYRAZOLO [4, 3-D] PYRIMIDINES USEFUL AS KINASE INHIBITORS<br/>[FR] PYRAZOLO[4,3-D]PYRIMIDINES UTILES EN TANT QU'INHIBITEURS DE KINASES
    申请人:ORIGENIS GMBH
    公开号:WO2012143144A1
    公开(公告)日:2012-10-26
    The present invention relates to novel compounds of formula (I) that are capable of inhibiting one or more kinases, especially SYK (Spleen Tyrosine Kinase), LRRK2 (Leucine-rich repeat kinase 2) and/or MYLK (Myosin light chain kinase) or mutants thereof. The compounds find applications in the treatment of a variety of diseases. These diseases include autoimmune diseases, inflammatory diseases, bone diseases, metabolic diseases, neurological and neurodegenerative diseases, cancer, cardiovascular diseases, allergies, asthma, alzheimer's disease, parkinson's disease, skin disorders, eye diseases, infectious diseases and hormone-related diseases.
    本发明涉及一种能够抑制一个或多个激酶,特别是SYK(脾酪氨酸激酶)、LRRK2(富含亮酸重复的激酶2)和/或MYLK(肌球蛋白轻链激酶)或其突变体的化合物的新颖化合物(I)的公式。这些化合物在治疗各种疾病中发挥作用。这些疾病包括自身免疫疾病、炎症性疾病、骨疾病、代谢性疾病、神经和神经退行性疾病、癌症、心血管疾病、过敏、哮喘、阿尔茨海默病、帕森病、皮肤疾病、眼部疾病、传染病和与激素相关的疾病。
  • [EN] HETEROCYCLIC COMPOUNDS AS KINASE INHIBITORS<br/>[FR] COMPOSÉS HÉTÉROCYCLIQUES EN TANT QU'INHIBITEURS DE KINASES
    申请人:ORIGENIS GMBH
    公开号:WO2012143143A1
    公开(公告)日:2012-10-26
    The present invention relates to novel compounds of formula (I) that are capable of inhibiting one or more kinases, especially SYK (Spleen Tyrosine Kinase), LRRK2 (Leucine-rich repeat kinase 2) and/or MYLK (Myosin light chain kinase) or mutants thereof. The compounds find applications in the treatment of a variety of diseases. These diseases include autoimmune diseases, inflammatory diseases, bone diseases, metabolic diseases, neurological and neurodegenerative diseases, cancer, cardiovascular diseases, allergies, asthma, alzheimer's disease, parkinson's disease, skin disorders, eye diseases, infectious diseases and hormone-related diseases.
    本发明涉及一种能够抑制一个或多个激酶,特别是SYK(脾酪氨酸激酶)、LRRK2(富含亮酸重复激酶2)和/或MYLK(肌球蛋白轻链激酶)或其突变体的化合物的新颖化合物(I)的公式。这些化合物在治疗各种疾病中发挥作用。这些疾病包括自身免疫疾病、炎症性疾病、骨疾病、代谢性疾病、神经和神经退行性疾病、癌症、心血管疾病、过敏、哮喘、阿尔茨海默病、帕森病、皮肤疾病、眼部疾病、传染病和与激素相关的疾病。
  • Novel Inhibitors of System Xc-
    申请人:The University of Montana, Missoula, MT
    公开号:US20150368213A1
    公开(公告)日:2015-12-24
    The present invention is directed to novel inhibitors of system X c − , also known as the cystine/glutamate antiporter. The present invention is further directed to methods of treating and detecting cancer that overexpresses system X c − which includes but is not limited to gliomas (including glioblastoma), triple negative breast cancer, and bladder cancer. The present invention is further directed to methods of treating seizures including epileptic seizures.
    本发明涉及新型系统Xc−抑制剂,也称为半胱酸/谷酸抗转运体。本发明还涉及治疗和检测过度表达系统Xc−的癌症的方法,其中包括但不限于胶质瘤(包括胶质母细胞瘤)、三阴性乳腺癌和膀胱癌。本发明还涉及治疗癫痫发作,包括癫痫发作的方法。
  • OXIDIZED AND MALEATED DERIVATIVE COMPOSITIONS
    申请人:Hurd Phillip W.
    公开号:US20090194731A1
    公开(公告)日:2009-08-06
    Oxidized and maleated derivative compositions, such as chemically modified oxidized and maleated tall oil fatty acid compositions, can be prepared and used in a variety of industrial applications, including as emulsifiers, corrosion inhibitors, concrete admixtures, and in reverse flotation mining applications.
    氧化和马来化衍生物组合物,例如经化学改性的氧化和马来化松香油脂酸组合物,可以制备并用于各种工业应用,包括作为乳化剂防腐剂、混凝土外加剂,以及逆浮选矿业应用中。
  • Diagnostic and therapeutic agents
    申请人:Taube Seija
    公开号:US20070258899A1
    公开(公告)日:2007-11-08
    Tumor targeting units are disclosed which have a peptide sequence C y —Y—G-F—X—W-G-Z-C yy (SEQ ID NO: 25), or a pharmaceutically or physiologically acceptable salt thereof. Tumor targeting agents are also disclosed having at least one targeting unit, directly or indirectly coupled to at least one effector unit. Diagnostic or pharmaceutical compositions having at least one targeting unit or at least one targeting agent, and targeting units or targeting agents for the preparation of a medicament for the treatment of cancer related diseases (including cancer), especially for the treatment of colon/colorectal cancer or its metastases are also disclosed.
    揭示了具有肽序列Cy—Y—G-F—X—W-G-Z-Cyy(序列ID编号:25)或其药学或生理上可接受的盐的肿瘤靶向单元。还披露了具有至少一个靶向单元的肿瘤靶向剂,直接或间接地偶联至至少一个效应单元。还披露了具有至少一个靶向单元或至少一个靶向剂的诊断或药物组合物,以及用于制备治疗癌症相关疾病(包括癌症)的药物的靶向单元或靶向剂,特别是用于治疗结肠/结直肠癌或其转移的靶向单元或靶向剂。
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