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MSI-1436 | 186139-09-3

中文名称
——
中文别名
——
英文名称
MSI-1436
英文别名
trodusquemine;aminosterol 1436;Trodulamine;[(3R,6R)-6-[(3S,5R,7R,8R,9S,10S,13R,14S,17R)-3-[3-[4-(3-aminopropylamino)butylamino]propylamino]-7-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptan-3-yl] hydrogen sulfate
MSI-1436化学式
CAS
186139-09-3
化学式
C37H72N4O5S
mdl
——
分子量
685.068
InChiKey
WUJVPODXELZABP-FWJXURDUSA-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):
    4.3
  • 重原子数:
    47
  • 可旋转键数:
    20
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    154
  • 氢给体数:
    6
  • 氢受体数:
    9

反应信息

  • 作为产物:
    描述:
    spermine tetrahydrochloride 、 potassium (5α,7α,24R)-7-hydroxy-3-ketocholestan-24-yl sulfate 以52的产率得到MSI-1436
    参考文献:
    名称:
    J. Nat. Prod. 2000, 63, 631-635
    摘要:
    DOI:
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文献信息

  • Novel phenyl-substituted imidazolidines, process for preparation thereof, medicaments comprising said compounds and use thereof
    申请人:JAEHNE Gerhard
    公开号:US20110178134A1
    公开(公告)日:2011-07-21
    The invention relates to compounds of formula (I) wherein the groups have stated meanings, and to their physiologically compatible salts. Said compounds are suitable, for example, as anti-obesity drugs and for treating cardiometabolic syndrome.
    本发明涉及具有所述意义的公式(I)的化合物,以及它们的生理相容性盐。所述化合物适用于例如作为抗肥胖药物和治疗心血管代谢综合征。
  • Arylchalcogenoarylalkyl-substituted imidazolidine-2,4-diones, process for preparation thereof, medicaments comprising these compounds and use thereof
    申请人:JAEHNE Gerhard
    公开号:US20110053947A1
    公开(公告)日:2011-03-03
    The invention relates to compounds of formula (I) wherein the groups R and R′, A, D, E, G, L, p and R1 to R10 have the stated meanings and to their physiologically compatible salts. Said compounds are suitable, for example, as anti-obesity drugs.
    本发明涉及具有公式(I)的化合物,其中R和R'、A、D、E、G、L、p以及R1至R10具有所述含义,以及它们的生理相容性盐。所述化合物例如可作为抗肥胖药物使用。
  • Arylaminoaryl-alkyl-substituted imidazolidine-2,4-diones, process for preparing them, medicaments comprising these compounds, and their use
    申请人:JAEHNE Gerhard
    公开号:US20090215728A1
    公开(公告)日:2009-08-27
    This invention relates to arylaminoaryl-alkyl-substituted imidazolidone-2,4-diones of formula (I) and also to their physiologically tolerated salts: Wherein R, R′, R1 to R10, A, D, E, G, L and p are as defined herein. The invention also relates to processes for preparing them, pharmaceutical compositions comprising them and their therapeutic use. The compounds are suitable, for example, as anti-obesity drugs and for treating cardiometabolic syndrome.
    这项发明涉及公式(I)中的芳基基芳基烷基取代的咪唑烷二酮及其生理耐受的盐: 其中R、R'、R1至R10、A、D、E、G、L和p如本文所定义。该发明还涉及制备它们的方法、包含它们的药物组合物以及它们的治疗用途。这些化合物适用于例如作为抗肥胖药物和治疗心脏代谢综合征。
  • Novel aromatic fluoroglycoside derivatives, pharmaceuticals comprising said compounds and the use thereof
    申请人:FRICK Wendelin
    公开号:US20110059910A1
    公开(公告)日:2011-03-10
    The invention relates to substituted aromatic fluoroglycoside derivatives, and to the physiologically compatible salts and physiologically functional derivatives thereof. The invention also relates to methods of lowering blood sugar and the treatment of type I and type II diabetes.
    这项发明涉及取代芳香族糖苷衍生物,以及其生理兼容盐和生理功能衍生物。该发明还涉及降低血糖和治疗I型和II型糖尿病的方法。
  • HETEROCYCLICALLY SUBSTITUTED METHOXYPHENYL DERIVATIVES WITH AN OXO GROUP, PROCESSES FOR PREPARATION THEREOF AND USE THEREOF AS MEDICAMENTS
    申请人:KEIL Stefanie
    公开号:US20120004165A1
    公开(公告)日:2012-01-05
    Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments The invention relates to heterocyclically substituted methoxyphenyl derivatives with an oxo group, and to physiologically compatible salts thereof. The invention relates to compounds of the formula I in which R1, R2, R3, R4, R10, X, n, B 1 , B 2 , B 3 and B 4 are each defined as specified, and to the physiologically compatible salts thereof. The compounds are suitable, for example, for treatment of diabetes.
    含有氧代基的杂环取代甲氧基苯基衍生物,其制备方法及用途作为药物。该发明涉及含有氧代基的杂环取代甲氧基苯基衍生物,以及其生理兼容盐。该发明涉及以下式I的化合物 其中R1、R2、R3、R4、R10、X、n、B1、B2、B3和B4分别如规定所定义,以及其生理兼容盐。这些化合物适用于例如糖尿病的治疗。
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