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2-phenyl-4,5-dihydro-1H-imidazole-4-carboxylic acid

中文名称
——
中文别名
——
英文名称
2-phenyl-4,5-dihydro-1H-imidazole-4-carboxylic acid
英文别名
——
2-phenyl-4,5-dihydro-1H-imidazole-4-carboxylic acid化学式
CAS
——
化学式
C10H10N2O2
mdl
——
分子量
190.2
InChiKey
VOYCCPFDTWHFGV-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):
    0.5
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    61.7
  • 氢给体数:
    2
  • 氢受体数:
    3

文献信息

  • Certain 4-aminomethyl-2-substituted imidazole derivatives and 2-aminomethyl-4-substituted imidazole derivatives: new classes of dopamine receptor subtype specific ligands
    申请人:Neurogen Corporation, Corporation of the State of Delaware
    公开号:US20030018025A1
    公开(公告)日:2003-01-23
    Disclosed are compounds of the formula: 1 wherein R 1 represents optionally substituted aryl, heteroaryl, arylalkyl, or cycloalkyl groups; X, Z, and Y are optionally substituted nitrogen or carbon atoms; R 3 and R 4 are organic or inorganic substitutents which may togther form ring structutes; m is zero, one or two; and R 5 and R 6 are are organic or inorganic substituents; and the pharmaceutically acceptable addition salts thereof, which compounds are highly selective partial agonists or antagonists at brain dopamine receptor subtypes or prodrugs thereof and are useful in the diagnosis and treatment of affective disorders such as schizophrenia and depression as well as certain movement disorders such as Parkinsonism.
    揭示了以下式的化合物: 其中R1代表可选择地取代的芳基、杂环芳基、芳基烷基或环烷基基团;X、Z和Y为可选择地取代的氮或碳原子;R3和R4为有机或无机取代基,可能共同形成环结构;m为零、一或二;R5和R6为有机或无机取代基; 以及其药学上可接受的盐, 这些化合物是高度选择性的部分激动剂或拮抗剂,作用于脑多巴胺受体亚型或其前药,并可用于诊断和治疗情感障碍,如精神分裂症和抑郁症,以及某些运动障碍,如帕金森病。
  • COMPOUNDS FOR TREATMENT OF CANCER
    申请人:Miller Duane D.
    公开号:US20090326020A1
    公开(公告)日:2009-12-31
    Compounds according to formula (I) are disclosed where Q is S, N, or O; X is optional, and can be O═, S═, ═N—NH 2 , ═N—OH, or —OH; Y is optional and can be —N(H)—, O, or C 1 to C 20 hydrocarbon; and R 1 and R 2 are each independently substituted or unsubstituted single-, fused- or multiple-ring aryl or (hetero)cyclic ring systems. Methods of making these compounds, pharmaceutical compositions containing the compounds, and their use, particularly for treating or preventing cancer, are also disclosed.
    根据公式(I)披露的化合物如下:其中Q为S、N或O;X为可选,可以是O═、S═、═N—NH2、═N—OH或—OH;Y为可选,可以是—N(H)—、O或C1至C20碳氢化合物;而R1和R2分别独立地为取代或未取代的单环、融合环或多环芳基或(杂)环烷基环系统。还披露了制备这些化合物的方法、含有这些化合物的药物组合物,以及它们的用途,特别是用于治疗或预防癌症。
  • Certain 4-aminomethyl-2-substituted imidazole derivatives and 2-aminomethyl-4-substituted imidazole derivatives; new classes of dopamine receptor subtype specific ligands
    申请人:Neurogen Corporation
    公开号:US20020143044A1
    公开(公告)日:2002-10-03
    Disclosed are compounds of the formula: 1 wherein R 1 represents optionally substituted aryl, heteroaryl, arylalkyl, or cycloalkyl groups; X, Z, and Y are optionally substituted nitrogen or carbon atoms; R 3 and R 4 are organic or inorganic substitutents which may together form ring structutes; m is zero, one or two; and R 5 and R 6 are are organic or inorganic substituents; and the pharmaceutically acceptable addition salts thereof, which compounds are highly selective partial agonists or antagonists at brain dopamine receptor subtypes or prodrugs thereof and are useful in the diagnosis and treatment of affective disorders such as schizophrenia and depression as well as certain movement disorders such as Parkinsonism.
    本发明涉及以下公式的化合物:1其中,R1代表可选取代的芳基,杂芳基,芳基烷基或环烷基基团;X,Z和Y是可选取代的氮或碳原子;R3和R4是有机或无机取代基,它们可以共同形成环结构;m为零,一或二;R5和R6是有机或无机取代基;以及其药学上可接受的盐。这些化合物是高度选择性的部分激动剂或拮抗剂,适用于诊断和治疗情感障碍,如精神分裂症和抑郁症以及某些运动障碍,如帕金森病。
  • COMPOUND FOR TREATMENT OF CANCER
    申请人:University of Tennessee Research Foundation
    公开号:EP2959900A1
    公开(公告)日:2015-12-30
    A compound, wherein the compound is (2-(1H-indol-3-yl)imidazol-4-yl)(3,4,5-trimethoxyphenyl)methanone. A pharmaceutical composition comprising the compound is (2-(1H-indol-3-yl)imidazol-4-yl)(3,4,5-trimethoxyphenyl)methanone and a pharmaceutically acceptable carrier. The compound (2-(1H-indol-3-yl)imidazol-4-yl)(3,4,5-trimethoxyphenyl)methanone for use in treating prostate cancer, breast cancer, ovarian cancer, skin cancer, lung cancer, colon cancer, leukemia, renal cancer or CNS cancer, or a combination thereof.
    一种化合物,其中化合物为(2-(1H-吲哚-3-基)咪唑-4-基)(3,4,5-三甲氧基苯基)甲酮。 一种药物组合物,包含化合物 (2-(1H-吲哚-3-基)咪唑-4-基)(3,4,5-三甲氧基苯基)甲酮和药学上可接受的载体。 (2-(1H-吲哚-3-基)咪唑-4-基)(3,4,5-三甲氧基苯基)甲酮化合物用于治疗前列腺癌、乳腺癌、卵巢癌、皮肤癌、肺癌、结肠癌、白血病、肾癌或中枢神经系统癌症,或它们的组合。
  • Compounds for treatment of cancer
    申请人:University of Tennessee Research Foundation
    公开号:US10301285B2
    公开(公告)日:2019-05-28
    The present invention relates to a compound of formula XXII and a compound of formula 17ya, which are defined as anywhere in the specification, to a composition comprising the same, and to a method of using thereof in the treatment of various forms of cancer.
    本发明涉及一种式 XXII 化合物和一种式 17ya 化合物(在说明书的任何地方都有定义),涉及一种包含这些化合物的组合物,还涉及一种将其用于治疗各种癌症的方法。
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