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5-Oxo-6-isopropyl-5,6-dihydropyrido<2,3-d>pyridazin | 66135-74-8

中文名称
——
中文别名
——
英文名称
5-Oxo-6-isopropyl-5,6-dihydropyrido<2,3-d>pyridazin
英文别名
6-isopropyl-6H-pyrido[2,3-d]pyridazin-5-one;6-Propan-2-ylpyrido[2,3-d]pyridazin-5-one
5-Oxo-6-isopropyl-5,6-dihydropyrido<2,3-d>pyridazin化学式
CAS
66135-74-8
化学式
C10H11N3O
mdl
——
分子量
189.217
InChiKey
JDXLCEUBZAGBLP-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):
    1
  • 重原子数:
    14
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    45.6
  • 氢给体数:
    0
  • 氢受体数:
    3

文献信息

  • SILICON BASED DRUG CONJUGATES AND METHODS OF USING SAME
    申请人:BlinkBio, Inc.
    公开号:US20170202970A1
    公开(公告)日:2017-07-20
    Described herein are silicon based conjugates capable of delivering one or more payload moieties to a target cell or tissue. Contemplated conjugates may include a silicon-heteroatom core, one or more optional catalytic moieties, a targeting moiety that permits accumulation of the conjugate within a target cell or tissue, one or more payload moieties (e.g., a therapeutic agent or imaging agent), and two or more non-interfering moieties covalently bound to the silicon-heteroatom core.
    本文描述了基于的共轭物,能够将一个或多个有效载荷基团传递到靶细胞或组织。考虑到的共轭物可能包括一个-杂原子核心,一个或多个可选的催化基团,一个定位基团,允许共轭物在靶细胞或组织内积累,一个或多个有效载荷基团(例如,治疗剂或成像剂),以及与-杂原子核心共价结合的两个或更多个不干扰基团。
  • Oxadiazole transient receptor potential channel inhibitors
    申请人:Genentech, Inc.
    公开号:US10710994B2
    公开(公告)日:2020-07-14
    The invention relates to compounds of formula I: and pharmaceutically acceptable salts thereof wherein A, X, R1, R4 and n are as defined herein. In addition, the present invention relates to methods of manufacturing and methods of using the compounds of formula I as well as pharmaceutical compositions containing such compounds. The compounds may be useful in treating diseases and conditions mediated by TRPA1, such as pain.
    本发明涉及式 I 的化合物: 及其药学上可接受的盐,其中 A、X、R1、R4 和 n 如本文所定义。此外,本发明还涉及式 I 化合物的制造方法和使用方法,以及含有此类化合物的药物组合物。这些化合物可用于治疗由 TRPA1 介导的疾病和病症,如疼痛。
  • OXADIAZOLE TRANSIENT RECEPTOR POTENTIAL CHANNEL INHIBITORS
    申请人:Genentech, Inc.
    公开号:US20200308161A1
    公开(公告)日:2020-10-01
    The invention relates to methods of using compounds formula I: and pharmaceutically acceptable salts thereof wherein A, X, R 1 , R 4 and n are as defined herein. In addition, the present invention relates to methods of manufacturing and methods of using the compounds of formula I as well as pharmaceutical compositions containing such compounds. The compounds may be useful in treating diseases and conditions mediated by TRPA1, such as pain.
  • US9931407B2
    申请人:——
    公开号:US9931407B2
    公开(公告)日:2018-04-03
  • [EN] SILICON BASED DRUG CONJUGATES AND METHODS OF USING SAME<br/>[FR] CONJUGUÉS DE MÉDICAMENT À BASE DE SILICIUM ET LEURS PROCÉDÉS D'UTILISATION
    申请人:BLINKBIO INC
    公开号:WO2016183359A1
    公开(公告)日:2016-11-17
    Described herein are silicon based conjugates capable of delivering one or more pay load moieties to a target cell or tissue. Contemplated conjugates may include a silicon-heteroatom core, one or more optional catalytic moieties, a targeting moiety that permits accumulation of the conjugate within a target cell or tissue, one or more pay load moieties (e.g., a therapeutic agent or imaging agent), and two or more non-interfering moieties covalently bound to the silicon-heteroatom core.
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