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(3E)-6-methyl-3-nitrohepta-1,3,5-triene

中文名称
——
中文别名
——
英文名称
(3E)-6-methyl-3-nitrohepta-1,3,5-triene
英文别名
——
(3E)-6-methyl-3-nitrohepta-1,3,5-triene化学式
CAS
——
化学式
C8H11NO2
mdl
——
分子量
153.18
InChiKey
PFHNFWKBZMTROB-SOFGYWHQSA-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):
    3
  • 重原子数:
    11
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    45.8
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • [EN] ARYL SULFAMIDE AND SULFAMATE DERIVATIVES AS RORc MODULATORS<br/>[FR] DÉRIVÉS D'ARYL SULFAMIDE ET DE SULFAMATE COMME MODULATEURS DE RORC
    申请人:HOFFMANN LA ROCHE
    公开号:WO2014140059A1
    公开(公告)日:2014-09-18
    Compounds of the formula I: or pharmaceutically acceptable salts thereof, wherein m, n, p, q, r, A, X1, X2, X3, X4, X5, X6, Y, Z, G, R1a, R2a, R1b, R2b, R3, R4, R5 and R6 are as defined herein. Also disclosed are methods of making the compounds and using the compounds for treatment of inflammatory diseases such as arthritis.
  • [EN] INHIBITORS OF CYCLIN-DEPENDENT KINASE 7 (CDK7)<br/>[FR] INHIBITEURS DE LA KINASE CYCLINE-DÉPENDANTE 7 (CDK7)
    申请人:SYROS PHARMACEUTICALS INC
    公开号:WO2015154039A2
    公开(公告)日:2015-10-08
    The present invention provides novel compounds of Formula (I) and Formula (II) and pharmaceutically acceptable salts, solvates, hydrates, tautomers, stereoisomers, isotopically labeled derivatives, and compositions thereof. Also provided are methods and kits involving the compounds or compositions for treating or preventing proliferative diseases (e.g., cancers (e.g., leukemia, melanoma, multiple myeloma), benign neoplasms, angiogenesis, inflammatory diseases, autoinflammatory diseases, and autoimmune diseases) in a subject. Treatment of a subject with a proliferative disease using a compound or composition of the invention may inhibit the aberrant activity of cyclin-dependent kinase 7 (CDK7), and therefore, induce cellular apoptosis and/or inhibit transcription in the subject.
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