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2-Brom-α-ergocryptin-<82Br> | 1214709-38-2

中文名称
——
中文别名
——
英文名称
2-Brom-α-ergocryptin-<82Br>
英文别名
2-Brom-α-ergokryptin;2-bromo-12'-hydroxy-5'-isobutyl-2'-isopropyl-ergotamane-18,3',6'-trione;(8S)-2-Bromo alpha-ergocryptine;5-bromo-N-[2-hydroxy-7-(2-methylpropyl)-5,8-dioxo-4-propan-2-yl-3-oxa-6,9-diazatricyclo[7.3.0.02,6]dodecan-4-yl]-7-methyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide
2-Brom-α-ergocryptin-<82Br>化学式
CAS
1214709-38-2
化学式
C32H40BrN5O5
mdl
——
分子量
654.604
InChiKey
OZVBMTJYIDMWIL-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):
    3.8
  • 重原子数:
    43
  • 可旋转键数:
    5
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.59
  • 拓扑面积:
    118
  • 氢给体数:
    3
  • 氢受体数:
    6

文献信息

  • COMPOUNDS FOR TREATMENTS OF INFLAMMATION
    申请人:Palmqvist Niklas
    公开号:US20120190751A1
    公开(公告)日:2012-07-26
    The present invention relates to the use of benzylideneaminoguanidines for the treatment of inflammation and pain. In one preferred embodiment, the invention relates to the use of N-(2-chloro-3,4-dimethoxybenzylideneamino)guanidine for the treatment of rheumatoid arthritis.
    本发明涉及使用苯甲醛胍基胍类化合物治疗炎症和疼痛。在一个优选实施例中,本发明涉及使用N-(2-氯-3,4-二甲氧基苯甲醛基)胍基胍治疗类风湿性关节炎。
  • Pharmaceutical agents for the treatment of cerebral amyloidosis
    申请人:NYMOX CORPORATION
    公开号:EP1930308A1
    公开(公告)日:2008-06-11
    The invention relates to a compound of the following general formula (III): wherein: R1 and R2 each are one or more independent substituents selected from the group consisting of hydrogen, C1-C5 alkyl, C2-C5 alkenyl, C3-C5 cycloalkyl, C1-C5 alkoxy, C2-C5 alkynyl, halogen, C1-C5 haloalkyl, alkylamino, phenyl, nitro and carboxyl; R3 is selected from the group consisting of amino, C1-C5 substituted amino and CH2; n and m are independently an integer of from 0-5; or a pharmaceutically acceptable salt of such compound; a compound of the following general formula (IV): wherein: R1 and R2 each are one or more independent substituents selected from the group consisting of hydrogen, C1-C5 alkyl, C2-C5 alkenyl, C3-C5 cycloalkyl, C1-C5 alkoxy, C2-C5 alkynyl, halogen, C1-C5 haloalkyl, alkylamino, phenyl, nitro and ca rboxyl; R3 and R4 each are independent and selected from the group consisting of hydrogen and C1-C5 alkyl; n is an integer of from 1 to 5; or a pharmaceutically acceptable salt of such compound; a compound of the following general formula (V): wherein: R1 and R2 each are one or more independent substituents selected from the group consisting of hydrogen, C1-C5 alkyl, C2-C5 alkenyl, C3-C5 cycloalkyl, C1-C5 alkoxy, C2-C5 alkynyl, halogen, C1-C5 haloalkyl, alkylamino, phenyl, nitro and carboxyl; R3 is selected from hydrogen and C1-C5 alkyl; R4 is selected from hydrogen and C1-C5 alkyl; n is an integer of from 1 to 5 inclusive; or a pharmaceutically acceptable salt of such compound; and a compound of the following general formula (VI): wherein: R1 and R2 each are one or more independent substituents selected from the group consisting of hydrogen, C1-C5 alkyl, C2-C5 alkenyl, C3-C5 cycloalkyl, C1-C5 alkoxy, C2-C5 alkynyl, halogen, C1-C5 haloalkyl, alkylamino, phenyl, nitro and carboxyl; R3 and R4 each are independent and selected from hydrogen and C1-C5 alkyl; n is an integer of from 1 to 5 inclusive; or a pharmaceutically acceptable salt of such compound. Also compositions comprising the compounds III-VI as well as uses of said compounds.
    本发明涉及以下通式 (III) 的化合物: 其中 R1和R2各自为一个或多个独立取代基,选自由氢、C1-C5烷基、C2-C5烯基、C3-C5环烷基、C1-C5烷氧基、C2-C5炔基、卤素、C1-C5卤代烷基、烷基氨基、苯基、硝基和羧基组成的组; R3 选自氨基、C1-C5 取代的氨基和 CH2 组成的组; n 和 m 独立地为 0-5 之间的整数; 或此类化合物的药学上可接受的盐; 以下通式(IV)的化合物: 其中 R1和R2各自是一个或多个独立的取代基,选自由氢、C1-C5烷基、C2-C5烯基、C3-C5环烷基、C1-C5烷氧基、C2-C5炔基、卤素、C1-C5卤代烷基、烷基氨基、苯基、硝基和羧基组成的组; R3 和 R4 各自独立,选自由氢和 C1-C5 烷基组成的组; n 是 1 至 5 的整数; 或此类化合物的药学上可接受的盐; 以下通式(V)的化合物: 其中 R1和R2各自为一个或多个独立取代基,选自由氢、C1-C5烷基、C2-C5烯基、C3-C5环烷基、C1-C5烷氧基、C2-C5炔基、卤素、C1-C5卤代烷基、烷基氨基、苯基、硝基和羧基组成的组; R3 选自氢和 C1-C5 烷基; R4 选自氢和 C1-C5 烷基; n 是 1 至 5(包括 5)的整数; 或此类化合物的药学上可接受的盐;以及 以下通式(VI)的化合物: 其中 R1和R2各自是一个或多个独立的取代基,选自由氢、C1-C5烷基、C2-C5烯基、C3-C5环烷基、C1-C5烷氧基、C2-C5炔基、卤素、C1-C5卤代烷基、烷基氨基、苯基、硝基和羧基组成的组; R3 和 R4 各自独立,选自氢和 C1-C5 烷基; n 是 1 至 5(包括 5)的整数; 或此类化合物的药学上可接受的盐。 还包括由化合物 III-VI 组成的组合物以及所述化合物的用途。
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