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3-氯-2-甲基-N-(4-(2-(4-甲基哌嗪-1-基)-2-氧代乙基)噻唑-2-基)苯磺酰胺 | 376640-41-4

中文名称
3-氯-2-甲基-N-(4-(2-(4-甲基哌嗪-1-基)-2-氧代乙基)噻唑-2-基)苯磺酰胺
中文别名
3-氯-2-甲基-n-(4-(2-(4-甲基哌嗪-1-基)-2-氧代乙基)噻唑-2-基)苯磺酰胺
英文名称
3-chloro-2-methyl-N-(4-(2-(4-methylpiperazin-1-yl)-2-oxoethyl)thiazol-2-yl)benzenesulfonamide
英文别名
3-chloro-2-methyl-N-[4-[2-(4-methylpiperazin-1-yl)-2-oxoethyl]-1,3-thiazol-2-yl]benzenesulfonamide
3-氯-2-甲基-N-(4-(2-(4-甲基哌嗪-1-基)-2-氧代乙基)噻唑-2-基)苯磺酰胺化学式
CAS
376640-41-4
化学式
C17H21ClN4O3S2
mdl
——
分子量
429.0
InChiKey
YDPRNGAPPNPYQQ-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):
    2
  • 重原子数:
    27
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    119
  • 氢给体数:
    1
  • 氢受体数:
    7

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。
  • CARBAMOYLBENZOTRIAZOLE DERIVATIVES AS INHIBITORS OF LIPASES AND PHOSPHOLIPASES
    申请人:Petry Stefan
    公开号:US20080287503A1
    公开(公告)日:2008-11-20
    The invention relates to carbamoylbenzotriazole derivatives of general formula (I), which are defined as cited in the description, to their pharmaceutically applicable salts and to their use as medicaments.
    这项发明涉及一般式(I)的氨基甲酰基苯并三唑衍生物,其在描述中被定义,以及它们的药用盐和作为药物的用途。
  • AZOLOPYRIDIN-3-ONE DERIVATIVES AS INHIBITORS OF LIPASES AND PHOSPHOLIPASES
    申请人:Petry Stefan
    公开号:US20130157941A1
    公开(公告)日:2013-06-20
    The present invention relates to azolopyridin-3-one derivatives of the general formula (I) with the meanings specified in the description, to their pharmaceutically usable salts and to their use as drug substances.
    本发明涉及通式(I)所示的咪唑吡啶-3-酮衍生物,其含义如描述中所指定的,以及它们的药用盐和作为药物物质的用途。
  • 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)中的芳基氨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。
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同类化合物

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