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4-(四甲基-1,3,2-二氧硼戊环-2-基)-6-(三氟甲基)-1H-吲唑 | 1454300-91-4

中文名称
4-(四甲基-1,3,2-二氧硼戊环-2-基)-6-(三氟甲基)-1H-吲唑
中文别名
——
英文名称
4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-6-(trifluoromethyl)-1H-indazole
英文别名
4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)-6-(trifluoromethyl)-1H-indazole
4-(四甲基-1,3,2-二氧硼戊环-2-基)-6-(三氟甲基)-1H-吲唑化学式
CAS
1454300-91-4
化学式
C14H16BF3N2O2
mdl
——
分子量
312.099
InChiKey
WTYDAYOWXTYIBG-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):
    2.88
  • 重原子数:
    22
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    47.1
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

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文献信息

  • INDAZOLE DERIVATIVES
    申请人:TAKEDA PHARMACEUTICAL COMPANY LIMITED
    公开号:US20150005232A1
    公开(公告)日:2015-01-01
    Disclosed are compounds of Formula 1, and pharmaceutically acceptable salts thereof, wherein R 1 , R 2 , R 3 , R 4 , R 5 , and R 6 are defined in the specification. This disclosure also relates to materials and methods for preparing compounds of Formula 1, to pharmaceutical compositions which contain them, and to their use for treating obesity and related diseases, disorders, and conditions associated with MetAP2.
    本发明涉及公式1的化合物及其药学上可接受的盐,其中R1、R2、R3、R4、R5和R6在规范中有定义。本发明还涉及制备公式1化合物的材料和方法,以及包含它们的制药组合物,并用于治疗肥胖症以及与MetAP2相关的疾病、失调和病症的用途。
  • Indazole derivatives
    申请人:TAKEDA PHARMACEUTICAL COMPANY LIMITED
    公开号:US09434743B2
    公开(公告)日:2016-09-06
    Disclosed are compounds of Formula 1, and pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4, R5, and R6 are defined in the specification. This disclosure also relates to materials and methods for preparing compounds of Formula 1, to pharmaceutical compositions which contain them, and to their use for treating obesity and related diseases, disorders, and conditions associated with MetAP2.
    本发明涉及1号式化合物及其药学上可接受的盐,其中R1、R2、R3、R4、R5和R6在规范中定义。本公开还涉及制备1号式化合物的材料和方法,包括含有它们的制药组合物,并且涉及使用它们治疗肥胖和与MetAP2相关的疾病、障碍和状况。
  • Discovery of potent, reversible MetAP2 inhibitors via fragment based drug discovery and structure based drug design—Part 1
    作者:Zacharia Cheruvallath、Mingnam Tang、Christopher McBride、Mallareddy Komandla、Joanne Miura、Thu Ton-Nu、Phil Erikson、Jun Feng、Pamela Farrell、J. David Lawson、Darin Vanderpool、Yiqin Wu、Douglas R. Dougan、Artur Plonowski、Corine Holub、Chris Larson
    DOI:10.1016/j.bmcl.2016.04.073
    日期:2016.6
    Methionine aminopeptidase 2 (MetAP2) is an enzyme that cleaves an N-terminal methionine residue from a number of newly synthesized proteins. Pre-clinical and clinical studies suggest that MetAP2 inhibitors could be used as a novel treatment for obesity. Herein we describe our use of fragment screening methods and structural biology to quickly identify and elaborate an indazole fragment into a series of reversible MetAP2 inhibitors with < 10 nM potency, excellent selectivity, and favorable in vitro safety profiles. (C) 2016 Elsevier Ltd. All rights reserved.
  • [EN] INDAZOLE DERIVATIVES<br/>[FR] DÉRIVÉS D'INDAZOLE
    申请人:TAKEDA PHARMACEUTICAL
    公开号:WO2013130855A1
    公开(公告)日:2013-09-06
    Disclosed are compounds of Formula 1, and pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4, R5, and R6 are defined in the specification. This disclosure also relates to materials and methods for preparing compounds of Formula 1, to pharmaceutical compositions which contain them, and to their use for treating obesity and related diseases, disorders, and conditions associated with MetAP2.
    公开了Formula 1的化合物及其药用盐,其中R1、R2、R3、R4、R5和R6在规范中有定义。本公开还涉及制备Formula 1化合物的材料和方法,含有这些化合物的药物组合物,以及它们用于治疗肥胖和与MetAP2相关的疾病、紊乱和症状的用途。
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