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salmon MCH

中文名称
——
中文别名
——
英文名称
salmon MCH
英文别名
4-[[2-[[24-[[2-[[2-[[2-[(2-amino-3-carboxypropanoyl)amino]-3-hydroxybutanoyl]amino]-4-methylsulfanylbutanoyl]amino]-5-(diaminomethylideneamino)pentanoyl]amino]-3,12-bis[3-(diaminomethylideneamino)propyl]-6-[(4-hydroxyphenyl)methyl]-21-(2-methylsulfanylethyl)-2,5,8,11,14,17,20,23,31-nonaoxo-9,18-di(propan-2-yl)-26,27-dithia-1,4,7,10,13,16,19,22,30-nonazabicyclo[30.3.0]pentatriacontane-29-carbonyl]amino]-3-(1H-indol-3-yl)propanoyl]amino]-5-[(1-carboxy-2-methylpropyl)amino]-5-oxopentanoic acid
salmon MCH化学式
CAS
——
化学式
C89H139N27O24S4
mdl
——
分子量
2099.5
InChiKey
ORRDHOMWDPJSNL-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):
    -5.9
  • 重原子数:
    144
  • 可旋转键数:
    46
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    945
  • 氢给体数:
    28
  • 氢受体数:
    32

反应信息

  • 作为反应物:
    描述:
    2-(4-bromophenyl)-1-(4-chlorophenyl)pentan-1-ol 、 salmon MCH 在 1-bromo-4-(2-(4-chlorophenyl)-1-propylpent-4-en-1-yl)benzene 作用下, 以The title compound is obtained as a 2.1:1 mixture of diastereomers的产率得到1-bromo-4-(2-(4-chlorophenyl)-1-propylpent-4-en-1-yl)benzene
    参考文献:
    名称:
    Glucagon receptor antagonist compounds, compositions containing such compounds and methods of use
    摘要:
    披露了胰高血糖素受体拮抗剂化合物。这些化合物对于治疗2型糖尿病及相关疾病非常有用。还包括药物组成物和治疗方法。
    公开号:
    US07968589B2
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文献信息

  • GLUCAGON RECEPTOR ANTAGONIST COMPOUNDS, COMPOSITIONS CONTAINING SUCH COMPOUNDS AND METHODS OF USE
    申请人:Stelmach John E.
    公开号:US20100004158A1
    公开(公告)日:2010-01-07
    Glucagon receptor antagonist compounds are disclosed. The compounds are useful for treating type 2 diabetes and related conditions. Pharmaceutical compositions and methods of treatment are also included. (I)
    本文披露了一种胰高血糖素受体拮抗剂化合物。该化合物可用于治疗2型糖尿病及相关疾病。本文还包括制药组合物和治疗方法。
  • Substituted Imidazole 4-Carboxamides as Cholecystokinin-1 Receptor Modulators
    申请人:Berger Richard
    公开号:US20090239862A1
    公开(公告)日:2009-09-24
    Certain novel substituted imidazole 4-carboxamides are ligands of the human cholecystokinin receptor and, in particular, are selective ligands of the human cholecystokinin-1 receptor (CCK-1R). They are therefore useful for the treatment, control, or prevention of diseases and disorders responsive to the modulation of CCK-1, such as obesity, and diabetes.
    某些新型取代咪唑4-羧酰胺是人胆囊收缩素受体的配体,尤其是人胆囊收缩素-1受体(CCK-1R)的选择性配体。它们因此可用于治疗、控制或预防对CCK-1调节敏感的疾病和疾病,如肥胖症和糖尿病。
  • Substituted imidazole 4-carboxamides as cholecystokinin-1 receptor modulators
    申请人:Merck Sharp & Dohme Corp.
    公开号:US07858629B2
    公开(公告)日:2010-12-28
    Certain novel substituted imidazole 4-carboxamides are ligands of the human cholecystokinin receptor and, in particular, are selective ligands of the human cholecystokinin-1 receptor (CCK-1R). They are therefore useful for the treatment, control, or prevention of diseases and disorders responsive to the modulation of CCK-1R, such as obesity, and diabetes.
    某些新型取代咪唑4-羧酰胺是人类胆囊收缩素受体的配体,特别是人类胆囊收缩素-1受体(CCK-1R)的选择性配体。它们因此可用于治疗、控制或预防对CCK-1R调节敏感的疾病和障碍,如肥胖症和糖尿病。
  • Substituted Aminopyrimidines as Cholecystokinin-1 Receptor Modulators
    申请人:Edmondson Scott
    公开号:US20100113492A1
    公开(公告)日:2010-05-06
    Certain novel substituted aminopyrimidines are ligands of the human cholecystokinin receptor and, in particular, are selective ligands of the human cholecystokinin-1 receptor (CCK-1R). They are therefore useful for the treatment, control, or prevention of diseases and disorders responsive to the modulation of CCK-1R, such as obesity, and diabetes.
    某些新型取代氨基嘧啶是人体胆囊收缩素受体的配体,特别是人体胆囊收缩素-1受体(CCK-1R)的选择性配体。因此,它们对于治疗、控制或预防对CCK-1R调节敏感的疾病和疾病是有用的,例如肥胖症和糖尿病。
  • Substituted imidazoles as bombesin receptor subtype-3 modulators
    申请人:Dobbelaar Peter H.
    公开号:US20100204236A1
    公开(公告)日:2010-08-12
    Certain novel substituted imidazoles are ligands of the human bombesin receptor and, in particular, are selective ligands of the human bombesin receptor subtype-3 (BRS-3). They are therefore useful for the treatment, control, or prevention of diseases and disorders responsive to the modulation of BRS-3, such as obesity, and diabetes.
    某些新型取代咪唑是人类炸弹肽受体的配体,特别是人类炸弹肽受体亚型-3(BRS-3)的选择性配体。因此,它们可用于治疗、控制或预防对BRS-3调节敏感的疾病和障碍,例如肥胖症和糖尿病。
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