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7-((R)-3,3-difluoro-5-((3R,4S,E)-3-hydroxy-4-methylnon-1-en-6-yn-1-yl)-2-oxopyrrolidin-1-yl)heptanoic acid | 1544280-85-4

中文名称
——
中文别名
——
英文名称
7-((R)-3,3-difluoro-5-((3R,4S,E)-3-hydroxy-4-methylnon-1-en-6-yn-1-yl)-2-oxopyrrolidin-1-yl)heptanoic acid
英文别名
7-[(5R)-3,3-difluoro-5-[(E,3R,4S)-3-hydroxy-4-methylnon-1-en-6-ynyl]-2-oxopyrrolidin-1-yl]heptanoic acid
7-((R)-3,3-difluoro-5-((3R,4S,E)-3-hydroxy-4-methylnon-1-en-6-yn-1-yl)-2-oxopyrrolidin-1-yl)heptanoic acid化学式
CAS
1544280-85-4
化学式
C21H31F2NO4
mdl
——
分子量
399.478
InChiKey
ZSUOOBFOIDLLEI-LPJXYHDHSA-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):
    3.6
  • 重原子数:
    28
  • 可旋转键数:
    11
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    77.8
  • 氢给体数:
    2
  • 氢受体数:
    6

文献信息

  • [EN] DIFLUOROLACTAM COMPOSITIONS FOR EP4-MEDIATED OSTEO RELATED DISEASES AND CONDITIONS<br/>[FR] COMPOSITIONS DE DIFLUOROLACTAME DESTINÉES À DES MALADIES ET DES AFFECTIONS OSSEUSES MÉDIÉES PAR EP4
    申请人:CAYMAN CHEMICAL CO INC
    公开号:WO2014015246A1
    公开(公告)日:2014-01-23
    Disclosed herein are compositions and methods of treating osteroporosis, bone fracture, bone loss, and increasing bone density by administration of compounds of formula (I) or compositions comprising a compound of formula (I) and a pharmaceutically acceptable carrier, wherein L1, L2, L4, R1, R4, R5, R6, and s are as defined in the specification.
    披露的是通过给予公式(I)化合物的组合物和方法来治疗骨质疏松症、骨折、骨丢失以及增加骨密度,其中组合物包含公式(I)的化合物和药用可接受的载体,其中L1、L2、L4、R1、R4、R5、R6和s按说明书定义。
  • SUBSTITUTED QUINAZOLINE INHIBITORS OF GROWTH FACTOR RECEPTOR TYROSINE KINASES
    申请人:Gant Thomas G.
    公开号:US20100075916A1
    公开(公告)日:2010-03-25
    The present invention relates to new substituted quinazoline inhibitors of vascular endothelial growth factor receptor tyrosine kinase, epidermal growth factor receptor tyrosine kinase, and/or REarranged during Transfection tyrosine kinase, pharmaceutical compositions thereof, and methods of use thereof.
    本发明涉及新的取代喹唑啉抑制剂,用于血管内皮生长因子受体酪氨酸激酶、表皮生长因子受体酪氨酸激酶和/或重排在转位期间酪氨酸激酶,以及其药物组合物和使用方法。
  • DIFLUOROLACTAM COMPOSITIONS FOR EP4-MEDIATED OSTEO RELATED DISEASES AND CONDITIONS
    申请人:Cayman Chemical Company, Inc.
    公开号:US20150174099A1
    公开(公告)日:2015-06-25
    Disclosed herein are compositions and methods of treating osteoporosis, bone fracture, bone loss, and increasing bone density by administration of compounds of formula (I) or compositions comprising a compound of formula (I) and a pharmaceutically acceptable carrier, wherein L 1 , L 2 , L 4 , R 1 , R 4 , R 5 , R 6 , and s are as defined in the specification.
    本文披露了使用式(I)化合物或包含式(I)化合物和药物可接受载体的组合物治疗骨质疏松症、骨折、骨质流失和增加骨密度的方法和组合物。其中,L1、L2、L4、R1、R4、R5、R6和s如规范中所定义。
  • DIFLUOROLACTAM COMPOUNDS AS EP4 RECEPTOR-SELECTIVE AGONISTS FOR USE IN THE TREATMENT OF EP4-MEDIATED DISEASES AND CONDITIONS
    申请人:Cayman Chemical Company, Inc.
    公开号:US20150175538A1
    公开(公告)日:2015-06-25
    Disclosed herein are compounds of formula (I) and therapeutic methods of treatment with compounds of formula (I), wherein L 1 , L 2 , L 4 , R 1 , R 4 , R 5 , R 6 , and s are as defined in the specification. Compounds of formula (I) are EP4 agonists useful in the treatment of glaucoma, neuropathic pain, and related disorders.
    本文公开了式(I)的化合物及使用该化合物的治疗方法,其中L1、L2、L4、R1、R4、R5、R6和s的定义如规范中所述。式(I)的化合物是EP4激动剂,可用于治疗青光眼、神经病性疼痛和相关疾病。
  • METHODS OF SYNTHESIZING A DIFLUOROLACTAM ANALOG
    申请人:CAYMAN CHEMICAL COMPANY, INC.
    公开号:US20160060253A1
    公开(公告)日:2016-03-03
    The present invention relates to processes and intermediates for preparing compounds of formula (IA), wherein R 1 , R 4 , R 5 , R 6 , and L 1 are as defined herein. Compounds of formula (IA) have been found useful as EP 4 receptor agonists useful in the treatment of glaucoma, osteoporosis, neuropathic pain, and related disorders.
    本发明涉及制备式(IA)化合物的过程和中间体,其中R1、R4、R5、R6和L1如本文所定义。式(IA)化合物已被发现在治疗青光眼、骨质疏松症、神经病性疼痛和相关疾病中作为EP4受体激动剂而有用。
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