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N-Methyl-3-methoxypiperidin | 54288-76-5

中文名称
——
中文别名
——
英文名称
N-Methyl-3-methoxypiperidin
英文别名
3-Methoxy-1-methylpiperidine
N-Methyl-3-methoxypiperidin化学式
CAS
54288-76-5
化学式
C7H15NO
mdl
——
分子量
129.202
InChiKey
NYOZCDTULQDYDI-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):
    0.7
  • 重原子数:
    9
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    12.5
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • Photochromic Indeno-Fused Ring Pyran Compounds
    申请人:Transitions Optical, Inc.
    公开号:US20150141661A1
    公开(公告)日:2015-05-21
    The present invention relates to photochromic indeno-fused ring pyran compounds represented by the following Formula (I-A): The present invention also relates to photochromic dichroic compounds, such as represented by Formula (I-A), in which (i) Z 2 is a group N—R 13 in which R 13 is a group L, and (ii) optionally at least one R 1 independently for each n is selected from a group L, in which the group L independently in each case is a lengthening group that provides the photochromic compound with dichroic properties, in accordance with some embodiments. The present invention also relates to photochromic articles, such as photochromic ophthalmic articles, that include one or more photochromic compounds according to the present invention, such as represented by Formula (I-A).
    本发明涉及由以下式(I-A)表示的光致变色吲哚融合环吡喃化合物。本发明还涉及光致二向色化合物,例如由式(I-A)表示,其中(i)Z2是一个N—R13基团,其中R13是一个L基团,以及(ii)对于每个n,可选地至少选择一个R1,每种情况下独立选择自L基团,其中每种情况下L基团是一个提供光致化合物二向色性能的延伸基团,符合某些实施例。本发明还涉及光致物品,例如光致眼科物品,包括根据本发明的一个或多个光致化合物,例如由式(I-A)表示。
  • [EN] COMPOUNDS AND USES THEREOF<br/>[FR] COMPOSÉS ET LEURS UTILISATIONS
    申请人:FOGHORN THERAPEUTICS INC
    公开号:WO2019152437A1
    公开(公告)日:2019-08-08
    The present disclosure features compounds useful for the treatment of BAF complex-related disorders.
    本公开涉及用于治疗BAF复合物相关疾病的化合物。
  • [EN] PIKFYVE KINASE INHIBITORS<br/>[FR] INHIBITEURS DE KINASE PIKFYVE
    申请人:ACURASTEM INCORPORATED
    公开号:WO2021163727A1
    公开(公告)日:2021-08-19
    The present invention relates to compounds useful as inhibitors of phosphatidylinositol-3-phosphate 5-kinase (PIKfyve) as well as their use for treating diseases and disorders associated with PIKfyve.
    本发明涉及作为磷脂酰肌醇-3-磷酸5-激酶(PIKfyve)抑制剂的化合物,以及它们用于治疗与PIKfyve相关的疾病和紊乱的用途。
  • [EN] METHODS AND COMPOUNDS FOR RESTORING MUTANT p53 FUNCTION<br/>[FR] MÉTHODES ET COMPOSÉS POUR LA RESTAURATION DE LA FONCTION DU P53 MUTANT
    申请人:PMV PHARMACEUTICALS INC
    公开号:WO2021061643A1
    公开(公告)日:2021-04-01
    Mutations in oncogenes and tumor suppressors contribute to the development and progression of cancer. The present disclosure describes compounds and methods to recover wild-type function to p53 mutants. The compounds of the present invention can bind to mutant p53 and restore the ability of the p53 mutant to bind DNA and activate downstream effectors involved in tumor suppression. The disclosed compounds can be used to reduce the progression of cancers that contain a p53 mutation.
    癌基因和肿瘤抑制基因的突变促成了癌症的发展和进展。本公开披露描述了一种恢复p53突变体野生型功能的化合物和方法。本发明的化合物可以结合突变型p53,并恢复p53突变体结合DNA并激活参与肿瘤抑制的下游效应子的能力。所披露的化合物可用于减少含有p53突变的癌症的进展。
  • [EN] SMALL MOLECULE AGONISTS OF MUCOLIPIN 1 AND USES THEREOF<br/>[FR] PETITES MOLÉCULES AGONISTES DE LA MUCOLIPINE 1 ET LEURS UTILISATIONS
    申请人:UNIV MICHIGAN REGENTS
    公开号:WO2021041866A1
    公开(公告)日:2021-03-04
    This invention is in the field of medicinal chemistry. In particular, the invention relates to a new class of small-molecules having a phenyl-sulfonic amide (or similar) structure which function as agonists of mucolipin 1 (ML1), and their use as therapeutics for the treatment of Duchenne muscular dystrophy (DMD) and related disorders.
    这项发明属于药物化学领域。特别是,该发明涉及一类新的小分子,具有苯磺酰胺(或类似)结构,作为肌球脂蛋白1(ML1)的激动剂,以及它们作为治疗杜氏肌肉萎缩症(DMD)和相关疾病的疗法的用途。
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