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2-methyl-6,7-dihydro-4H-pyrano[3,4-d][1,3]thiazole

中文名称
——
中文别名
——
英文名称
2-methyl-6,7-dihydro-4H-pyrano[3,4-d][1,3]thiazole
英文别名
——
2-methyl-6,7-dihydro-4H-pyrano[3,4-d][1,3]thiazole化学式
CAS
——
化学式
C7H9NOS
mdl
——
分子量
155.22
InChiKey
VNDZFRHLQNLWMM-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):
    1.1
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    50.4
  • 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。
  • [EN] BIARYL COMPOUNDS USEFUL FOR THE TREATMENT OF HUMAN DISEASES IN ONCOLOGY, NEUROLOGY AND IMMUNOLOGY<br/>[FR] COMPOSÉS BIARYLIQUES UTILES POUR LE TRAITEMENT DE MALADIES HUMAINES EN ONCOLOGIE, NEUROLOGIE ET IMMUNOLOGIE
    申请人:BIOGEN IDEC INC
    公开号:WO2015089337A1
    公开(公告)日:2015-06-18
    The present invention provides compounds and compositions thereof which are useful as inhibitors of Bruton's tyrosine kinase and which exhibit desirable characteristics for the same.
    本发明提供了作为布鲁顿酪氨酸激酶抑制剂并具有相同理想特性的化合物及其组合物。
  • VIRAL REPLICATION INHIBITORS
    申请人:KATHOLIEKE UNIVERSITEIT LEUVEN, K.U. LEUVEN R&D
    公开号:US20140213586A1
    公开(公告)日:2014-07-31
    The present invention relates to a series of novel compounds, methods to prevent or treat viral infections in animals by using the novel compounds and to said novel compounds for use as a medicine, more preferably for use as a medicine to treat or prevent viral infections, particularly infections with RNA viruses, more particularly infections with viruses belonging to the family of the Flaviviridae, and yet more particularly infections with the Dengue virus. The present invention furthermore relates to pharmaceutical compositions or combination preparations of the novel compounds, to the compositions or preparations for use as a medicine, more preferably for the prevention or treatment of viral infections. The invention also relates to processes for preparation of the compounds.
    本发明涉及一系列新化合物,使用这些新化合物预防或治疗动物的病毒感染的方法,以及这些新化合物的药物用途,更好地用于治疗或预防病毒感染,特别是RNA病毒感染,更特别是属于黄病毒科的病毒感染,更进一步地是登革热病毒感染。本发明还涉及新化合物的药物组成物或复合制剂,以及用于预防或治疗病毒感染的药物组成物或制剂。本发明还涉及化合物的制备方法。
  • NOVEL VIRAL REPLICATION INHIBITORS
    申请人:Katholieke Universiteit Leuven
    公开号:EP2978753B1
    公开(公告)日:2020-08-12
  • BIARYL COMPOUNDS USEFUL FOR THE TREATMENT OF HUMAN DISEASES IN ONCOLOGY, NEUROLOGY AND IMMUNOLOGY
    申请人:Biogen MA Inc.
    公开号:EP3080103B1
    公开(公告)日:2018-04-18
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