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Bms-347070 | 197438-73-6

中文名称
——
中文别名
——
英文名称
Bms-347070
英文别名
(3Z)-3-[(4-bromophenyl)-(4-methylsulfonylphenyl)methylidene]oxolan-2-one
Bms-347070化学式
CAS
197438-73-6
化学式
C18H15BrO4S
mdl
——
分子量
407.3
InChiKey
KOWIZHDULJSRPT-WUKNDPDISA-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):
    4.1
  • 重原子数:
    24
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    68.8
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    生成 Bms-347070
    参考文献:
    名称:
    US6180651B1
    摘要:
    公开号:
点击查看最新优质反应信息

文献信息

  • NOUVEAUX DERIVES DIARYLMETHYLIDENE FURANIQUES, LEURS PROCEDES DE PREPARATION ET LEURS UTILISATIONS EN THERAPEUTIQUE
    申请人:LABORATOIRES UPSA
    公开号:EP0891345B1
    公开(公告)日:2001-08-16
  • COFORMULATION METHODS AND THEIR PRODUCTS
    申请人:Bradford Particle Design Limited
    公开号:EP1207856A2
    公开(公告)日:2002-05-29
  • Formulations of low solubility bioactive agents and processes for making the same
    申请人:——
    公开号:US20040185110A1
    公开(公告)日:2004-09-23
    A method of coprocessing a limited solubility bioactive agent with a compatible aid comprising: (a) identifying a compatible aid for the bioactive agent; (b) either (i) forming a co-dissolved solution of the compatible aid and bioactive agent in a common solvent or (ii) forming a solution of the compatible aid in an anti-solvent and forming solution of the bioactive agent in a solvent; and (c) forming a film or primary particles from the co-dissolved solution or solutions of step (b), which film or primary particles comprise bioactive agent in crystalline form, with the crystals having average diameter of 1 micron or less.
  • [EN] COFORMULATION METHODS AND THEIR PRODUCTS<br/>[FR] PROCEDES DE COFORMULATION ET LEURS PRODUITS
    申请人:BRADFORD PARTICLE DESIGN PLC
    公开号:WO2001015664A2
    公开(公告)日:2001-03-08
    A coformulation of an active (preferably pharmaceutically active, for instance a COX-2 enzyme inhibitor) substance and an oligomeric or polymeric excipient, containing at least 10 % of the active, between 80 and 100 % of which is amorphous. The amorphous phase is stable, with respect to the crystalline phase(s), for at least theree months after its preparation when stored at between O and 10 °C. The invention also provides processes, preferably involving SEDSTM particle formation, for preparing such a coformulation.
  • [EN] FORMULATIONS OF LOW SOLUBILITY BIOACTIVE AGENTS AND PROCESSES FOR MAKING THE SAME<br/>[FR] PREPARATIONS D'AGENTS BIOACTIFS PEU SOLUBLES ET PROCEDES POUR LES PRODUIRE
    申请人:BRISTOL MYERS SQUIBB CO
    公开号:WO2004043358A2
    公开(公告)日:2004-05-27
    A method of coprocessing a limited solubility bioactive agent with a compatible aid comprising: (a) identifying a compatible aid for the bioactive agent; (b) either (i) forming a co-dissolved solution of the compatible aid and bioactive agent in a common solvent or (ii) forming a solution of the compatible aid in an anti-solvent and forming solution of the bioactive agent in a solvent; and (c) forming a film or primary particles from the co-dissolved solution or solutions of step (b), which film or primary particles comprise bioactive agent in crystalline form, with the crystals having average diameter of 1 micron or less.
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