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suloctidil | 54767-75-8

中文名称
——
中文别名
——
英文名称
suloctidil
英文别名
(1S,2R)-2-(octylamino)-1-[4-(propan-2-ylthio)phenyl]-1-propanol;(1S,2R)-2-(octylamino)-1-(4-propan-2-ylsulfanylphenyl)propan-1-ol
suloctidil化学式
CAS
54767-75-8
化学式
C20H35NOS
mdl
——
分子量
337.57
InChiKey
BFCDFTHTSVTWOG-YLJYHZDGSA-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

物化性质

  • 熔点:
    62.5°C
  • 沸点:
    467.3±35.0 °C(Predicted)
  • 密度:
    0.9880 (rough estimate)
  • 溶解度:
    可溶于DMSO(少许)、甲醇(少许)

计算性质

  • 辛醇/水分配系数(LogP):
    5.8
  • 重原子数:
    23
  • 可旋转键数:
    12
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.7
  • 拓扑面积:
    57.6
  • 氢给体数:
    2
  • 氢受体数:
    3

安全信息

  • 危险品标志:
    Xn
  • 安全说明:
    S36
  • 危险类别码:
    R22
  • WGK Germany:
    3
  • RTECS号:
    DO8910000

SDS

SDS:d6044b5da11a460b32cdc6192fb91641
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制备方法与用途

概述

舒洛地尔是一种钙通道阻滞剂,具有抗血管痉挛和抗血栓形成的作用。研究发现,它在体外能够抑制白假丝酵母菌的生长;另有研究表明,舒洛地尔联合氟康唑使用时,对新型隐球菌有抑制作用。

用途

舒洛地尔的中文别名是索罗克替。作为一种强效的抗血小板药物,临床上主要用于治疗血栓。

文献信息

  • Methods for Screening Interleukin-6 (IL-6) Signal Transduction Inhibitors
    申请人:Kitamura Toshio
    公开号:US20090280483A1
    公开(公告)日:2009-11-12
    The present invention provides methods for screening compounds which inhibit activation of a member of the IL-6 signaling pathways, comprising: (a) a positive screening step using a cell capable of being killed by IL-6 stimulation to select compounds which inhibit death of the cell when it is stimulated by IL-6; and then (b) a biochemical screening step to further select compounds which inhibit activation of a member of the IL-6 signaling pathways by a biochemical means from the compounds selected in step (a). The present invention also provides compounds which inhibit activation of a member of the IL-6 signaling pathways identified using said methods.
  • SSAT mRNA TRANSLATION REPRESSION AND ACTIVATION
    申请人:Merali Salim
    公开号:US20140234827A1
    公开(公告)日:2014-08-21
    The invention provides an isolated nucleic acid having a sequence encoding a spermidine/spermine acetyltransferase (“SSAT”), wherein translation of an mRNA comprising the encoded SSAT has increased basal translation and increased stimulated translation, compared to a wild-type mRNA encoding SSAT. Methods of use for the nucleic acid are also provided. Methods and compositions are also provided for reducing ischemia-reperfusion injury in organs or tissue for transplantation.
  • COMPOSITIONS AND METHODS OF USE THEREOF FOR TREATMENT OF PROTEINOPATHIES
    申请人:Washington University
    公开号:US20210228591A1
    公开(公告)日:2021-07-29
    The present disclosure relates generally compositions and methods of using the same for the treatment of proteinopathies (e.g. Alpha-1-antitrypsin deficiency, Non-alcoholic fatty liver disease, Alzheimer's disease, Parkinson's disease, Amyotrophic Lateral Sclerosis, and Huntington's disease) with one or more proteotoxicity reducing agents.
  • US9585380B2
    申请人:——
    公开号:US9585380B2
    公开(公告)日:2017-03-07
  • [EN] COMPOSITIONS AND METHODS OF USE THEREOF FOR TREATMENT OF PROTEINOPATHIES<br/>[FR] COMPOSITIONS ET PROCÉDÉS D'UTILISATION DE CELLES-CI POUR LE TRAITEMENT DE PROTÉINOPATHIES
    申请人:UNIV WASHINGTON
    公开号:WO2019204764A1
    公开(公告)日:2019-10-24
    The present disclosure relates generally compositions and methods of using the same for the treatment of proteinopathies (e.g. Alpha-1-antitrypsin deficiency, Non-alcoholic fatty liver disease, Alzheimer's disease, Parkinson's disease, Amyotrophic Lateral Sclerosis, and Huntington's disease) with one or more proteotoxicity reducing agents.
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同类化合物

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