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rel-1,1-Dimethylethyl (3R,4R)-4-amino-3-phenyl-1-piperidinecarboxylate | 1160260-42-3

中文名称
——
中文别名
——
英文名称
rel-1,1-Dimethylethyl (3R,4R)-4-amino-3-phenyl-1-piperidinecarboxylate
英文别名
tert-butyl (3R,4R)-4-amino-3-phenylpiperidine-1-carboxylate
rel-1,1-Dimethylethyl (3R,4R)-4-amino-3-phenyl-1-piperidinecarboxylate化学式
CAS
1160260-42-3
化学式
C16H24N2O2
mdl
——
分子量
276.37
InChiKey
KTKQDEYFBRXGAI-UONOGXRCSA-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):
    2.1
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.56
  • 拓扑面积:
    55.6
  • 氢给体数:
    1
  • 氢受体数:
    3

文献信息

  • NITROGEN-CONTAINING HETEROCYCLIC COMPOUND AND USE OF SAME
    申请人:Shirai Junya
    公开号:US20110178060A1
    公开(公告)日:2011-07-21
    The present invention relates to a compound represented by the formula wherein ring A is a nitrogen-containing heterocycle; ring B is an aromatic ring optionally having substituent(s); ring D is an aromatic ring optionally having substituent(s); L is a group represented by the formula R 2 , R 3 , R 4a and R 4b are each independently a hydrogen atom, an optionally halogenated C 1-6 alkyl group or an optionally halogenated C 3-6 cycloalkyl group, or R 2 and R 3 are optionally bonded via an alkylene chain or an alkenylene chain, or R 4a and R 4b are optionally bonded via an alkylene chain or an alkenylene chain; R 1 is a hydrogen atom or a substituent; m and n are each independently an integer of 0 to 5; m+n is an integer of 2 to 5; and is a single bond or double bond, or a salt thereof; and the like. The compound has a superior tachykinin receptor antagonistic action, and is useful as an agent for the prophylaxis or treatment of various diseases such as lower urinary tract diseases, digestive tract diseases, central neurological disease and the like.
    本发明涉及一种化合物,其表示为式: 其中,环A是一种含氮杂环;环B是一种芳香环,可选地具有取代基;环D是一种芳香环,可选地具有取代基;L是一个代表式为R2、R3、R4a和R4b的基团,其中R2、R3、R4a和R4b各自独立地是氢原子、可选卤代的C1-6烷基或可选卤代的C3-6环烷基,或者R2和R3通过烷基链或烯基链可选地连接,或者R4a和R4b通过烷基链或烯基链可选地连接;R1是氢原子或取代基;m和n各自独立地为0到5的整数;m+n是2到5的整数;以及为单键或双键,或其盐;等等。该化合物具有优良的缩氨酸受体拮抗作用,并可用作预防或治疗各种疾病的药剂,如下尿路疾病、消化道疾病、中枢神经系统疾病等。
  • HETEROCYCLIC COMPOUND
    申请人:Takeda Pharmaceutical Company Limited
    公开号:EP3287441A1
    公开(公告)日:2018-02-28
    The present invention relates to a compound which can be useful for the treatment or prevention of SPT-related diseases including cancer and congenital diseases associated with sphingolipid accumulation (including Niemann-Pick disease).
    本发明涉及一种化合物,该化合物可用于治疗或预防与 SPT 有关的疾病,包括癌症和与鞘脂蓄积有关的先天性疾病(包括尼曼-皮克病)。
  • Heterocyclic compound
    申请人:TAKEDA PHARMACEUTICAL COMPANY LIMITED
    公开号:US10189785B2
    公开(公告)日:2019-01-29
    The present invention relates to a compound which can be useful for the treatment or prevention of SPT-related diseases including cancer and congenital diseases associated with sphingolipid accumulation (including Niemann-Pick disease).
    本发明涉及一种化合物,该化合物可用于治疗或预防与 SPT 有关的疾病,包括癌症和与鞘脂蓄积有关的先天性疾病(包括尼曼-皮克病)。
  • ACYLATED 4-AMINOPIPERIDINES AS INHIBITORS OF SERINE PALMITOYLTRANSFERASE
    申请人:Takeda Pharmaceutical Company Limited
    公开号:EP3287441B1
    公开(公告)日:2021-06-09
  • USRE48334E1
    申请人:——
    公开号:USRE48334E1
    公开(公告)日:2020-12-01
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