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(2E)-2-[2-(2-环己基乙基)肼亚基]丙酸

中文名称
(2E)-2-[2-(2-环己基乙基)肼亚基]丙酸
中文别名
糖尿病相关肽(胰岛淀粉样肽)(抗原);恩林肽
英文名称
(2S)-N-[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-4-amino-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-4-amino-1-[[(2S)-4-amino-1-[[(2S)-1-[[2-[[(2S)-1-[[(2S,3S)-1-[[(2S)-1-[[(2S)-1-[[(2S)-1-[[(2S,3R)-1-[[(2S)-4-amino-1-[[(2S)-1-[[2-[[(2S)-1-[[(2S)-4-amino-1-[[(2S,3R)-1-[[(2S)-1-amino-3-(4-hydroxyphenyl)-1-oxopropan-2-yl]amino]-3-hydroxy-1-oxobutan-2-yl]amino]-1,4-dioxobutan-2-yl]amino]-3-hydroxy-1-oxopropan-2-yl]amino]-2-oxoethyl]amino]-3-methyl-1-oxobutan-2-yl]amino]-1,4-dioxobutan-2-yl]amino]-3-hydroxy-1-oxobutan-2-yl]amino]-3-hydroxy-1-oxopropan-2-yl]amino]-3-hydroxy-1-oxopropan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-3-methyl-1-oxopentan-2-yl]amino]-1-oxopropan-2-yl]amino]-2-oxoethyl]amino]-1-oxo-3-phenylpropan-2-yl]amino]-1,4-dioxobutan-2-yl]amino]-1,4-dioxobutan-2-yl]amino]-3-hydroxy-1-oxopropan-2-yl]amino]-3-hydroxy-1-oxopropan-2-yl]amino]-3-(1H-imidazol-4-yl)-1-oxopropan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-1-oxo-3-phenylpropan-2-yl]amino]-1,4-dioxobutan-2-yl]amino]-1-oxopropan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-5-carbamimidamido-1-oxopentan-2-yl]-2-[[(2S,3R)-2-[[(2S)-2-[[(4R,7S,10S,13S,16S,19R)-16-(2-amino-2-oxoethyl)-19-[[(2S)-2,6-diaminohexanoyl]amino]-7,13-bis[(1R)-1-hydroxyethyl]-10-methyl-6,9,12,15,18-pentaoxo-1,2-dithia-5,8,11,14,17-pentazacycloicosane-4-carbonyl]amino]propanoyl]amino]-3-hydroxybutanoyl]amino]pentanediamide
英文别名
——
(2E)-2-[2-(2-环己基乙基)肼亚基]丙酸化学式
CAS
——
化学式
C165H261N51O55S2
mdl
——
分子量
3903.3
InChiKey
PLOPBXQQPZYQFA-AXPWDRQUSA-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):
    -18.7
  • 重原子数:
    273
  • 可旋转键数:
    115
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    1810
  • 氢给体数:
    61
  • 氢受体数:
    61

文献信息

  • Phenoxypiperidines and analogs thereof useful as histamine H3 antagonists
    申请人:Mutahi W. Mwangi
    公开号:US20070167435A1
    公开(公告)日:2007-07-19
    Disclosed are compounds of the formula or a pharmaceutically acceptable salt or solvate thereof, wherein: M is CH or N; U and W are each CH, or one of U and W is CH and the other is N; X is a bond, alkylene, —C(O)—, —C(N—OR 5 )—, —C(N—OR 5 )—CH(R 6 )—, —CH(R 6 )—C(N—OR 5 )—, —O—, —OCH 2 —, —CH 2 O— or —S(O) 0-2 —; Y is —O—, —(CH 2 ) 2 —, —C(═O)—, —C(═NOR 7 )— or —SO 0-2 —; Z is a bond, optionally substituted alkylene or alkylene interrupted by a heteroatom or heterocyclic group; R 1 is optionally substituted alkyl, cycloalkyl, aryl, arylalkyl, heteroaryl, heterocycloalkyl, or benzimidazolyl or a derivative thereof; R 2 is optionally substituted alkyl, alkenyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, cycloalkyl or heterocycloalkyl; and the remaining variables are as defined in the specification; compositions and methods for treating an allergy-induced airway response, congestion, diabetes, obesity, an obesity-related disorder, metabolic syndrome and a cognition deficit disorder using said compounds, alone or in combination with other agents.
    揭示了以下化合物的结构式或其药学上可接受的盐或溶剂,其中:M为CH或N;U和W分别为CH,或者U和W中的一个为CH,另一个为N;X为键,烷基,—C(O)—,—C(N—OR5)—,—C(N—OR5)—CH(R6)—,—CH(R6)—C(N—OR5)—,—O—,—OCH2—,—CH2O—或—S(O)0-2—;Y为—O—,—(CH2)2—,—C(═O)—,—C(═NOR7)—或—SO0-2—;Z为键,可选择地取代的烷基或被杂原子或杂环基中断的烷基;R1为可选择地取代的烷基,环烷基,芳基,芳基烷基,杂芳基,杂环烷基或苯并咪唑基或其衍生物;R2为可选择地取代的烷基,烯基,芳基,芳基烷基,杂芳基,杂芳基烷基,环烷基或杂环烷基;其余变量如规范中所定义;使用这些化合物,单独或与其他药剂联合使用,治疗由过敏引起的气道反应、充血、糖尿病、肥胖症、与肥胖有关的疾病、代谢综合征和认知缺陷障碍的组合物和方法。
  • [EN] FUSED BICYCLIC PYRIMIDINE DERIVATIVES AND METHODS OF USE THEREOF<br/>[FR] DÉRIVÉS DE PYRIMIDINE BICYCLIQUES FUSIONNÉES ET LEURS PROCÉDÉS D'UTILISATION
    申请人:SCHERING CORP
    公开号:WO2011062885A1
    公开(公告)日:2011-05-26
    The present invention relates to Fused Bicyclic Pyrimidine Derivatives, compositions comprising a Fused Bicyclic Pyrimidine Derivative, and methods of using the Fused Bicyclic Pyrimidine Derivatives for treating or preventing obesity, diabetes, a metabolic disorder, a cardiovascular disease or a disorder related to the activity of a G-protein coupled receptor (GPCR) in a patient.
    本发明涉及融合双环嘧啶衍生物,包含融合双环嘧啶衍生物的组合物,以及利用融合双环嘧啶衍生物治疗或预防肥胖、糖尿病、代谢紊乱、心血管疾病或与患者体内G蛋白偶联受体(GPCR)活性相关的疾病的方法。
  • [EN] BICYCLIC HETEROCYCLE DERIVATIVES AND USE THEREOF AS GPR119 MODULATORS<br/>[FR] DÉRIVÉS HÉTÉROCYCLIQUES BICYCLIQUES ET LEUR UTILISATION EN TANT QUE MODULATEURS DE GPR119
    申请人:SCHERING CORP
    公开号:WO2009143049A1
    公开(公告)日:2009-11-26
    The present invention relates to Bicyclic Heterocycle Derivatives of formula (I), compositions comprising a Bicyclic Heterocycle Derivative, and methods of using the Bicyclic Heterocycle Derivatives for treating or preventing obesity, diabetes, a metabolic disorder, a cardiovascular disease or a disorder related to the activity of GPR1 19 in a patient.
    本发明涉及公式(I)的双环杂环衍生物,包含双环杂环衍生物的组合物,以及使用双环杂环衍生物治疗或预防患者的肥胖、糖尿病、代谢紊乱、心血管疾病或与GPR119活性相关的疾病的方法。
  • TRICYCLIC SPIROCYCLE DERIVATIVES AND METHODS OF USE
    申请人:McCormick Kevin D.
    公开号:US20110166124A1
    公开(公告)日:2011-07-07
    The present invention relates to novel Tricyclic Spirocycle Derivatives, pharmaceutical compositions comprising the Tricyclic Spirocycle Derivatives and the use of these compounds for treating or preventing allergy, an allergy-induced airway response, congestion, a cardiovascular disease, an inflammatory disease, a gastrointestinal disorder, a neurological disorder, a metabolic disorder, obesity or an obesity-related disorder, diabetes, a diabetic complication, impaired glucose tolerance or aired fasting glucose.
    本发明涉及新型三环螺环衍生物,包括该三环螺环衍生物的药物组合物,以及利用这些化合物治疗或预防过敏、过敏引起的气道反应、充血、心血管疾病、炎症性疾病、消化系统紊乱、神经系统紊乱、代谢紊乱、肥胖或与肥胖相关的疾病、糖尿病、糖尿病并发症、糖耐量受损或空腹血糖异常。
  • 1-[[1-[(2-Amino-6-methyl-4-pyridinyl)methyl]-4-fluoro-4-piperidinyl]carbonyl]-4-[2-(2-pyridinyl)-3H-imidazo[4,5-b]pyridin-3-yl]piperidine
    申请人:de Lera Ruiz Manuel
    公开号:US20070066644A1
    公开(公告)日:2007-03-22
    The present invention discloses the compound of Formula I and pharmaceutically acceptable salts and solvates thereof. The invention also relates to pharmaceutical compositions comprising the Compound of Formula I and its use in treating obesity, metabolic syndrome, diabetes, hepatic lipidosis or nonalcoholic fatty liver disease. The invention also relates to the use of a combination of the Compound of Formula I with additional therapeutic agents for treating obesity, metabolic syndrome, diabetes, hepatic lipidosis or nonalcoholic fatty liver disease.
    本发明公开了化合物I的结构以及其药学上可接受的盐和溶剂化合物。该发明还涉及包括化合物I的药物组合物,并且其在治疗肥胖症、代谢综合征、糖尿病、肝脂肪病或非酒精性脂肪肝病中的用途。该发明还涉及将化合物I与其他治疗剂的组合物用于治疗肥胖症、代谢综合征、糖尿病、肝脂肪病或非酒精性脂肪肝病。
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