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1-[1-(2-naphthalen-1-yl-ethanesulfonyl)-piperidin-4-yl]-1,4-dihydro-benzo[d][1,3]oxazin-2-one | 844683-99-4

中文名称
——
中文别名
——
英文名称
1-[1-(2-naphthalen-1-yl-ethanesulfonyl)-piperidin-4-yl]-1,4-dihydro-benzo[d][1,3]oxazin-2-one
英文别名
1-[1-(2-naphthalen-1-ylethylsulfonyl)piperidin-4-yl]-4H-3,1-benzoxazin-2-one
1-[1-(2-naphthalen-1-yl-ethanesulfonyl)-piperidin-4-yl]-1,4-dihydro-benzo[d][1,3]oxazin-2-one化学式
CAS
844683-99-4
化学式
C25H26N2O4S
mdl
——
分子量
450.558
InChiKey
KNDKNFRSWVGGFG-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):
    4.3
  • 重原子数:
    32
  • 可旋转键数:
    5
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.32
  • 拓扑面积:
    75.3
  • 氢给体数:
    0
  • 氢受体数:
    5

文献信息

  • [EN] NEW ACETYL COENZYME A CARBOXYLASE (ACC) INHIBITORS AND USES IN TREATMENTS OF OBESITY AND DIABETES MELLITUS - 087<br/>[FR] NOUVEAUX INHIBITEURS DE L'ACÉTYL COENZYME A CARBOXYLASE (ACC) ET UTILISATIONS DANS LE TRAITEMENT DE L'OBÉSITÉ ET DU DIABÈTE SUCRÉ - 087
    申请人:ASTRAZENECA AB
    公开号:WO2009082346A1
    公开(公告)日:2009-07-02
    The present invention relates to Acetyl Coenzyme A Carboxylase (ACC) inhibitors according to formula (I), or an enantiomer thereof, or a pharmaceutically acceptable salt thereof, where R1, R2, R3, R4, R5, E, L, Z and n are as defined herein, to processes for preparing such compounds, to pharmaceutical compositions containing them, to the use of such inhibitors and to methods for th eir therapeutic use, particularly in the treatments of obesity and diabetes mellitus.
    本发明涉及根据式(I)的乙酰辅酶A羧化酶(ACC)抑制剂,或其对映体,或其药用可接受的盐,其中R1、R2、R3、R4、R5、E、L、Z和n的定义如本文所述,以及制备此类化合物的方法,含有它们的药物组合物,使用这种抑制剂以及用于它们的治疗用途的方法,特别是用于肥胖和糖尿病的治疗。
  • [EN] ACTIVE SUBSTANCE COMBINATION COMPRISING A COMPOUND WITH NPY RECEPTOR AFFINITY AND A COMPOUND WITH 5-HT6 RECEPTOR AFFINITY<br/>[FR] COMBINAISON DE SUBSTANCES ACTIVES COMPORTANT UN COMPOSE A AFFINITE DE RECEPTEUR NPY ET UN COMPOSE A AFFINITE DE RECEPTEUR 5-HT6
    申请人:ESTEVE LABOR DR
    公开号:WO2005014000A1
    公开(公告)日:2005-02-17
    The present invention relates to an active substance combination comprising at least one compound with neuropeptide Y-receptor affinity and at least one compound with 5-HT6 receptor affinity, a medicament comprising said active substance combination, and the use of said active substance combination for the manufacture of a medicament.
    本发明涉及一种活性物质组合,包括至少一种具有神经肽Y受体亲和力的化合物和至少一种具有5-HT6受体亲和力的化合物,以及包含所述活性物质组合的药物和利用该活性物质组合制造药物的用途。
  • Active substance combination comprising a compound with npy receptor affinity and a compound with 5-ht6 receptor affinity
    申请人:Torrens Jover Antoni
    公开号:US20070009597A1
    公开(公告)日:2007-01-11
    The present invention relates to an active substance combination comprising at least one compound with neuropeptide Y-receptor affinity, preferably neuropeptide Y5-receptor affinity, and at least one compound with 5-HT 6 receptor affinity, a medicament comprising said active substance combination, and the use of said active substance combination for the manufacture of a medicament.
    本发明涉及一种活性物质组合,包括至少一种具有神经肽Y受体亲和力的化合物,优选为神经肽Y5受体亲和力,以及至少一种具有5-HT6受体亲和力的化合物,一种包含该活性物质组合的药物,以及使用该活性物质组合制造药物。
  • Benzoxazinone-derived sulfonamide compounds, their preparation and use as medicaments
    申请人:Torrens Jover Antoni
    公开号:US20070032482A1
    公开(公告)日:2007-02-08
    The present invention relates to benzoxazinone-derived sulphonamide compounds of general formula (I), a process for their preparation, a medicament comprising these compounds and the use of benzoxazinone-derived sulphonamide compounds for the preparation of medicaments for 5-HT 6 receptor regulation as well as for the treatment of disorders related thereto.
    本发明涉及一般式(I)的苯并噁唑酮衍生磺酰胺化合物,其制备过程,包含这些化合物的药物以及苯并噁唑酮衍生磺酰胺化合物用于制备5-HT6受体调节剂药物以及治疗与之相关的疾病。
  • ACTIVE SUBSTANCE COMBINATION COMPRISING A COMPOUND WITH NPY RECEPTOR AFFINITY AND A COMPOUND WITH 5-HT6 RECEPTOR AFFINITY
    申请人:Torrens Jover Antoni
    公开号:US20120128768A1
    公开(公告)日:2012-05-24
    The present invention relates to an active substance combination comprising at least one compound with neuropeptide Y-receptor affinity and at least one compound with 5-HT6 receptor affinity, a medicament comprising said active substance combination, and the use of said active substance combination for the manufacture of a medicament.
    本发明涉及一种活性物质组合物,包括至少一种具有神经肽Y受体亲和力的化合物和至少一种具有5-HT6受体亲和力的化合物,以及包含该活性物质组合物的药物和使用该活性物质组合物制造药物的用途。
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