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3-(3,5-dibromo-4-(4-hydroxy-3-iso-propylphenylsulfonyl)phenyl)propionic acid

中文名称
——
中文别名
——
英文名称
3-(3,5-dibromo-4-(4-hydroxy-3-iso-propylphenylsulfonyl)phenyl)propionic acid
英文别名
3-[3,5-Dibromo-4-(4-hydroxy-3-propan-2-ylphenyl)sulfonylphenyl]propanoic acid
3-(3,5-dibromo-4-(4-hydroxy-3-iso-propylphenylsulfonyl)phenyl)propionic acid化学式
CAS
——
化学式
C18H18Br2O5S
mdl
——
分子量
506.212
InChiKey
GYMREZBGMZNQRW-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):
    4.6
  • 重原子数:
    26
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    100
  • 氢给体数:
    2
  • 氢受体数:
    5

文献信息

  • METHOD OF TREATING HAIR LOSS USING SULFONYL THYROMIMETIC COMPOUNDS
    申请人:UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER
    公开号:EP1185232A1
    公开(公告)日:2002-03-13
  • US5284971A
    申请人:——
    公开号:US5284971A
    公开(公告)日:1994-02-08
  • US6646005B1
    申请人:——
    公开号:US6646005B1
    公开(公告)日:2003-11-11
  • [EN] METHOD OF TREATING HAIR LOSS USING SULFONYL THYROMIMETIC COMPOUNDS<br/>[FR] METHODE DE TRAITEMENT DE LA PERTE DES CHEVEUX A L'AIDE DE COMPOSES DE SULFONYLE THYROMIMETIQUES
    申请人:UNIV TEXAS SOUTHWESTERN MED CT
    公开号:WO2000072810A1
    公开(公告)日:2000-12-07
    A method of treating hair loss comprising administering a composition comprising a cardiac-sparing compound characterized by structure (I) and pharmaceutically acceptable salts, hydrates, and biohydrolyzable amides, esters, and imides thereof, wherein: R1 is -(CH2)n(CHNR7R8)mC(O)R9; n is an integer from 1 to 3; m is an integer from 0 to 1; R3 and R5 are each, independently, selected from the group consisting of chlorine, bromine, iodine, and -CH3, R7 and R8 are each, independently, selected from the group consisting of hydrogen and C1-C4 alkyl; R9 is selected from the group consisting of hydroxy, C1-C4 alkoxy, and -NR7R8; R31 is selected from the group consisting of hydrogen, chlorine, bromine, iodine, C1-C4 alkyl, C4-C6 cycloalkyl, C1-C4 haloalkyl, C4-C6 halocycloalkyl, and -CH(R10)Ar; Ar is selected from the group consisting of 5-hydroxypyrid-2-yl, 6-hydroxypyrid-3-yl, 6-hydroxypyridazin-3-yl, 6-methoxypyridazin-3-yl N-oxide, and 6-hydroxypyridazin-3-yl N-oxide; R10 is selected from the group consisting of hydrogen and C1-C4 alkyl; and R41 is selected from the group consisting of hydroxy and C1-C4 alkoxy.
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