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(R)-N-Cyanomethyl-3-[2-(1,1-difluoro-methoxy)-phenylmethanesulfonyl]-2-(naphthalene-2-sulfonylamino)-propionamide | 330475-37-1

中文名称
——
中文别名
——
英文名称
(R)-N-Cyanomethyl-3-[2-(1,1-difluoro-methoxy)-phenylmethanesulfonyl]-2-(naphthalene-2-sulfonylamino)-propionamide
英文别名
(2R)-N-(cyanomethyl)-3-[[2-(difluoromethoxy)phenyl]methylsulfonyl]-2-(naphthalen-2-ylsulfonylamino)propanamide
(R)-N-Cyanomethyl-3-[2-(1,1-difluoro-methoxy)-phenylmethanesulfonyl]-2-(naphthalene-2-sulfonylamino)-propionamide化学式
CAS
330475-37-1
化学式
C23H21F2N3O6S2
mdl
——
分子量
537.565
InChiKey
FLLRDSGLTTVRHJ-FQEVSTJZSA-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):
    3.1
  • 重原子数:
    36
  • 可旋转键数:
    11
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    159
  • 氢给体数:
    2
  • 氢受体数:
    10

文献信息

  • Novel compounds and compositions as cathepsin S inhititors
    申请人:AXYS PHARMACEUTICALS, INC.
    公开号:US20040014796A1
    公开(公告)日:2004-01-22
    The present invention relates to novel selective cathepsin S inhibitors, the pharmaceutically acceptable salts and N-oxides thereof, their uses as therapeutic agents and the methods of their making.
    本发明涉及新型选择性卡痕蛋白S抑制剂,其药学上可接受的盐和N-氧化物,它们作为治疗剂的用途以及它们的制备方法。
  • COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS AS CATHEPSIN S INHIBITORS
    申请人:AXYS PHARMACEUTICALS, INC.
    公开号:EP1212302A1
    公开(公告)日:2002-06-12
  • USE OF CATHEPSIN S INHIBITORS FOR TREATING AN IMMUNE RESPONSE CAUSED BY ADMINISTRATION OF A SMALL MOLECULE THERAPEUTIC OR BIOLOGIC
    申请人:AXYS PHARMACEUTICALS, INC.
    公开号:EP1694357A1
    公开(公告)日:2006-08-30
  • US6492362B1
    申请人:——
    公开号:US6492362B1
    公开(公告)日:2002-12-10
  • [EN] COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS AS CATHEPSIN S INHIBITORS<br/>[FR] COMPOSES ET COMPOSITIONS PHARMACEUTIQUES UTILISES COMME INHIBITEURS DE LA CATHEPSINE S
    申请人:AXYS PHARM INC
    公开号:WO2001019796A1
    公开(公告)日:2001-03-22
    The present invention relates to novel selective cathepsin S inhibitors, the pharmaceutically acceptable salts and N-oxides thereof, their uses as therapeutic agents and the methods of their making.
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