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2-(3-Mesityl-2,5,7-trimethyl-8H-pyrazolo[1,5-a]pyrrolo[3,2-e]pyrimidin-8-yl)ethyl propyl ether | 344290-81-9

中文名称
——
中文别名
——
英文名称
2-(3-Mesityl-2,5,7-trimethyl-8H-pyrazolo[1,5-a]pyrrolo[3,2-e]pyrimidin-8-yl)ethyl propyl ether
英文别名
4,7,11-Trimethyl-3-(2-propoxyethyl)-10-(2,4,6-trimethylphenyl)-1,3,8,12-tetrazatricyclo[7.3.0.02,6]dodeca-2(6),4,7,9,11-pentaene
2-(3-Mesityl-2,5,7-trimethyl-8H-pyrazolo[1,5-a]pyrrolo[3,2-e]pyrimidin-8-yl)ethyl propyl ether化学式
CAS
344290-81-9
化学式
C25H32N4O
mdl
——
分子量
404.555
InChiKey
KJWLEQJNOAJKIW-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):
    5.3
  • 重原子数:
    30
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    44.4
  • 氢给体数:
    0
  • 氢受体数:
    3

文献信息

  • Fused heterotricyclic compounds, process for preparing the compounds and drugs containing the same
    申请人:——
    公开号:US20030078277A1
    公开(公告)日:2003-04-24
    The present invention provides a novel compound having an excellent corticotrophin-releasing-factor receptor antagonistic activity. That is, it provides a compound represented by the following formula, a pharmacologically acceptable salt thereof or hydrates thereof. 1 Wherein A, B and D are the same as or different from each other and each represents a group represented by the formula —(CR 1 R 2 ) m — (wherein R 1 and R 2 are the same as or different from each other and each represents a C 1-6 alkyl group etc.), —NR 3 — (wherein R 3 represetns hydrogen etc.) etc.; E and G are the same as or different from each other and each represents a group represented by the formula —(CR 6 R 7 ) p — (wherein R 6 and R 7 are the same as or different from each other and each represents hydrogen etc.; and p represents an integer of 0, 1 or 2); J represents a carbon atom or nitrogen atom, each substituted with C 1-6 alkyl group optionally substituted with a halogen atom, etc.; K and L are the same as or different from each other and each represents carbon atom or nitrogen atom; M means hydrogen, a halogen atom, an optionally substituted C 1-6 alkyl group etc.; and the partial structure means a single or double bond.
    本发明提供了一种具有优异的促肾上腺皮质激素释放因子受体拮抗活性的新化合物。即提供了由以下公式表示的化合物,其药理学上可接受的盐或合物。其中A、B和D相互相同或不同,每个代表以下公式表示的基团:—(CR1R2)m—(其中R1和R2相互相同或不同,每个代表C1-6烷基等),—NR3—(其中R3代表氢等)等;E和G相互相同或不同,每个代表以下公式表示的基团:—(CR6R7)p—(其中R6和R7相互相同或不同,每个代表氢等;p代表0、1或2的整数);J代表一个碳原子或氮原子,每个都被C1-6烷基等可选择地取代的卤素原子等取代;K和L相互相同或不同,每个代表碳原子或氮原子;M代表氢、卤素原子、可选择地取代的C1-6烷基等;部分结构表示单键或双键。
  • Antagonist of MCP-1 function, and compositions and methods of use thereof
    申请人:——
    公开号:US20040198719A1
    公开(公告)日:2004-10-07
    Compounds of formula A and formula B: 1 and their pharmaceutically acceptable salts, compositions comprising them, methods for their use, and their use in the preparation of medicaments. The compounds are antagonists of MCP-1 function, and are useful in the prevention and treatment of chronic or acute inflammatory or autoimmune diseases, such as multiple sclerosis, and in the prevention and treatment of allergic hypersensitivity disorders.
    公式A和公式B的化合物及其药学上可接受的盐,包括它们的组合物,使用方法以及它们在药物制备中的应用。这些化合物是MCP-1功能的拮抗剂,可用于预防和治疗慢性或急性炎症或自身免疫性疾病,如多发性硬化症,并用于预防和治疗过敏性过敏反应性疾病。
  • Tricyclic fused heterocyclic compounds as CRFantagonists
    申请人:Eisai Co., Ltd.
    公开号:EP1408040A1
    公开(公告)日:2004-04-14
    The present invention provides a novel compound having an excellent corticotrophin-releasing-factor receptor antagonistic activity. That is, it provides a compound represented by the following formula, a pharmacologically acceptable salt thereof or hydrates thereof. wherein: R2 is a hydrogen atom, a C1-6 alkyl group, a C2-6 alkenyl group, a C2-6 alkynyl group, a C1-6 alkoxy group, a C3-8 cycloalkyl group, a C1-6 alkoxy C1-6 alkyl group, a C3-8 cycloalkyl C1-6 alkyl group or a C1-6 alkyl-aryl group; the partial structure --- represents a single or double bond; M' represents a hydrogen atom, a halogen atom or a C1-6 alkyl group; R7' represents a hydrogen atom or a C1-6 alkyl group; W' represents an optionally substituted aryl group or an optionally substituted saturated or unsaturated heterocyclic ring; and R3 is a hydrogen atom or various specific organic substituents.
    本发明提供了一种新型化合物,它具有优异的促肾上腺皮质激素释放因子受体拮抗活性。也就是说,本发明提供了由下式表示的化合物、其药理学上可接受的盐或其合物。 其中 R2 是氢原子、C1-6 烷基、C2-6 烯基、C2-6 炔基、C1-6 烷氧基、C3-8 环烷基、C1-6 烷氧基 C1-6 烷基、C3-8 环烷基 C1-6 烷基或 C1-6 烷基芳基; 部分结构----代表单键或双键; M' 代表氢原子、卤素原子或 C1-6 烷基; R7' 代表氢原子或 C1-6 烷基; W' 代表任选取代的芳基或任选取代的饱和或不饱和杂环;以及 R3 是氢原子或各种特定的有机取代基。
  • US6951865B2
    申请人:——
    公开号:US6951865B2
    公开(公告)日:2005-10-04
  • US6962926B2
    申请人:——
    公开号:US6962926B2
    公开(公告)日:2005-11-08
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