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1-<β-(2,6-Dichlorbenzyloxy)-p-chlorphenethyl>-imidazol | 22833-02-9

中文名称
——
中文别名
——
英文名称
1-<β-(2,6-Dichlorbenzyloxy)-p-chlorphenethyl>-imidazol
英文别名
1-[2-(4-chloro-phenyl)-2-(2,6-dichloro-benzyloxy)-ethyl]-1H-imidazole;orconazole;1-[2-(4-chlorophenyl)-2-[(2,6-dichlorophenyl)methoxy]ethyl]imidazole
1-<β-(2,6-Dichlorbenzyloxy)-p-chlorphenethyl>-imidazol化学式
CAS
22833-02-9
化学式
C18H15Cl3N2O
mdl
——
分子量
381.689
InChiKey
PBNSEYNKZBMLLY-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):
    4.7
  • 重原子数:
    24
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    27
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • Enhanced propertied pharmaceuticals
    申请人:——
    公开号:US20040254182A1
    公开(公告)日:2004-12-16
    This invention relates to compounds which are useful as enhanced propertied pharmaceutical compounds for both human and veterinary application. The pharmaceutical compounds which are suitable for use in this invention are those compounds which can be substituted with a moiety, said moiety comprising a substituent which enhances or changes the properties of the pharmaceutical compound. The chemical modification of drugs into labile derivatives with enhanced physicochemical properties that enable better transport through biological barriers is a useful approach for improving-drug delivery.
    这项发明涉及一种化合物,该化合物可用作增强性质的药用化合物,适用于人类和兽医应用。适用于本发明的药用化合物是那些可以被取代为一种基团的化合物,该基团包括一种增强或改变药用化合物性质的取代基。将药物化学修饰为具有增强的物理化学性质的不稳定衍生物,从而能够更好地穿过生物屏障,这是改善药物输送的一种有用方法。
  • Diagnostic/therapeutic agents
    申请人:Klaveness Jo
    公开号:US20050002865A1
    公开(公告)日:2005-01-06
    Targetable diagnostic and/or therapeutically active agents, e.g. ultrasound contrast agents, comprising a suspension in an aqueous carrier liquid of a reporter comprising gas-containing or gas-generating material, said agent being capable of forming at least two types of binding pairs with a target.
    可定位的诊断和/或治疗活性剂,例如超声对比剂,包括悬浮在水载体液中的报告物,该报告物包含含气体或生成气体的材料,该剂能够与目标形成至少两种结合对。
  • Novel pharmaceutical agents containing carbohydrate moieties and methods of their preparation and use
    申请人:Christian T. Samuel
    公开号:US20060189547A1
    公开(公告)日:2006-08-24
    Hydrophilic N-linked pharmaceutical compositions, methods of their preparation and use in neuraxial drug delivery comprising a glycosyl CNS acting prodrug compound covalently N-linked with a saccharide through an amide or an amine bond and a formulary consisting of an additive, a stabilizer, a carrier, a binder, a buffer, an excipient, an emollient, a disintegrant, a lubricating agent, an antimicrobial agent or a preservative, with the proviso that the saccharide moiety is not a cyclodextrin or a glucuronide.
    亲水性N-连接药物组合物,其制备方法和在神经轴向药物输送中的使用,包括一种糖基中枢神经系统作用前药化合物,通过酰胺或胺键与糖苷共价连接,并且配方包括添加剂、稳定剂、载体、粘合剂、缓冲剂、赋形剂、润肤剂、破碎剂、润滑剂、抗微生物剂或防腐剂,但前提是糖苷基团不是环糊精或葡萄糖醛酸盐。
  • Novel Pharmaceutical Agents Containing Carbohydrate Moieties And Methods Of Their Preparation And Use
    申请人:Christian Samuel T.
    公开号:US20110237544A1
    公开(公告)日:2011-09-29
    Hydrophilic N-linked pharmaceutical compositions, methods of their preparation and use in neuraxial drug delivery comprising a glycosyl CNS acting prodrug compound covalently N-linked with a saccharide through an amide or an amine bond and a formulary consisting of an additive, a stabilizer, a carrier, a binder, a buffer, an excipient, an emollient, a disintegrant, a lubricating agent, an antimicrobial agent or a preservative, with the proviso that the saccharide moiety is not a cyclodextrin or a glucuronide.
    亲水性N-连接的药物组成物、其制备方法和在神经轴药物输送中的使用,包括一种糖基CNS作用的前药化合物,通过酰胺或胺键与糖分子共价连接,并由添加剂、稳定剂、载体、粘合剂、缓冲剂、赋形剂、润肤剂、崩解剂、润滑剂、抗微生物剂或防腐剂组成的制剂,前提是糖分子部分不是环糊精或葡糖醛酸盐。
  • Antifungal dermatological solution
    申请人:ORTHO PHARMACEUTICAL CORPORATION
    公开号:EP0156507A1
    公开(公告)日:1985-10-02
    Alcohol aqueous solutions of certain relatively insoluble imidazole derivatives. particularly miconazole and miconazole nitrate, are prepared to concentrations of at least 1.0 percent by weight active agent. The solutions are pharmacologically acceptable for topical application as the treatment of fungal skin infections and are readily applied by means of a pump sprayer.
    某些相对不溶性咪唑衍生物(尤其是咪康唑和硝酸咪康唑)的酒精水溶液可配制成活性剂浓度至少为 1.0%(重量百分比)的溶液。这些溶液在药理上可用于治疗真菌性皮肤感染的局部用药,并可通过泵式喷雾器方便地使用。
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