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2-(吡咯烷-1-基)乙烷硫醇 | 42302-16-9

中文名称
2-(吡咯烷-1-基)乙烷硫醇
中文别名
——
英文名称
2-(pyrrolidin-1-yl)ethane-1-thiol
英文别名
2-(pyrrolidin-1-yl)ethanethiol;2-pyrrolidin-1-ylethanethiol
2-(吡咯烷-1-基)乙烷硫醇化学式
CAS
42302-16-9
化学式
C6H13NS
mdl
MFCD11190758
分子量
131.242
InChiKey
FJOXVWJOCNVDDI-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):
    1.3
  • 重原子数:
    8
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    4.2
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2933990090

SDS

SDS:63d041c5a1564feb4d644b6fc756f393
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反应信息

  • 作为反应物:
    描述:
    2-(吡咯烷-1-基)乙烷硫醇4-fluorophenyl 2-[4-[2-(1-pyrrolidinyl)ethoxy]phenyl]benzo[b]thiophen-3-yl ketone 在 sodium hydride 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 5.25h, 以73%的产率得到(2-[4-[2-(1-pyrrolidinyl)ethoxy]phenyl]benzo[b]thiophen-3-yl)-(4-[[2-(1-pyrrolidinyl)ethyl]thio]phenyl)ketone
    参考文献:
    名称:
    Diamino Benzo[b]thiophene Derivatives as a Novel Class of Active Site Directed Thrombin Inhibitors. 5. Potency, Efficacy, and Pharmacokinetic Properties of Modified C-3 Side Chain Derivatives
    摘要:
    A systematic investigation of the structure-activity relationships of the C-3 side chain of the screening hit la led to the identification of the potent thrombin inhibitors 23c, 28c, and 31c. Their activities (1240, 903, and 1271 x 10(6) L/mol, respectively) represent 2200- and 2900-fold increases in potency over the starting lead la. This activity enhancement was accomplished with an increase of thrombin selectivity. The in vitro anticoagulant profiles of derivatives 28c and 31c were determined, and they compare favorably with the clinical agent H-R-1-[4aS,-8aS]perhydroisoquinolyl-prolyl-arginyl aldehyde (D-Piq-Pro-Arg-H; 32). The more potent members of this series have been studied in an arterial/venous shunt (AV shunt) model of thrombosis and were found to be efficacious in reducing clot formation. However, their efficacy is currently limited by their rapid and extensive distribution following administration.
    DOI:
    10.1021/jm9903388
  • 作为产物:
    描述:
    、 sodium hydroxide 作用下, 以 乙醇 为溶剂, 反应 3.0h, 生成 2-(吡咯烷-1-基)乙烷硫醇
    参考文献:
    名称:
    [EN] NOVEL CYCLOSPORIN DERIVATIVES AND USES THEREOF
    [FR] NOUVEAUX DÉRIVÉS DE CYCLOSPORINE ET LEURS UTILISATIONS
    摘要:
    公开号:
    WO2014145686A3
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文献信息

  • Aryl compounds with aminoalkyl substituents and their use
    申请人:Härter Michael
    公开号:US20110312930A1
    公开(公告)日:2011-12-22
    The present application relates to novel aryl compounds with aminoalkyl substituents, to processes for their preparation, to their use for treatment and/or prevention of diseases and to their use for the preparation of medicaments for treatment and/or prevention of diseases, in particular for treatment and/or prevention of hyperproliferative and angiogenic diseases and those diseases which arise from metabolic adaptation to hypoxic states. Such treatments can be carried out as monotherapy or also in combination with other medicaments or further therapeutic measures.
    本申请涉及具有氨基烷基取代基的新型芳基化合物,涉及其制备方法,涉及它们用于治疗和/或预防疾病以及用于制备治疗和/或预防疾病的药物的用途,特别是用于治疗和/或预防过度增殖和血管生成性疾病以及那些由于代谢适应低氧状态而引起的疾病。这种治疗可以作为单独治疗进行,也可以与其他药物或进一步的治疗措施结合使用。
  • [EN] SUBSTITUTED PYRAZOLO[1,5-A]PYRIDINE COMPOUNDS AS RET KINASE INHIBITORS<br/>[FR] COMPOSÉS DE PYRAZOLO[1,5-A]PYRIDINE SUBSTITUÉS EN TANT QU'INHIBITEURS DE LA KINASE RET
    申请人:ANDREWS STEVEN W
    公开号:WO2018071454A1
    公开(公告)日:2018-04-19
    Provided herein are compounds of the Formula I: (I) or pharmaceutically acceptable salt or solvate thereof, wherein A, B, X1, X2, X3, X4, Ring D, E, Ra, Rb, n and m have the meanings given in the specification, which are inhibitors of RET kinase and are useful in the treatment and prevention of diseases which can be treated with a RET kinase inhibitor, including RET-associated diseases and disorders.
    本文提供了Formula I的化合物:(I)或其药用可接受的盐或溶剂,其中A、B、X1、X2、X3、X4、环D、E、Ra、Rb、n和m的含义如规范中所述,它们是RET激酶的抑制剂,并且在治疗和预防可以用RET激酶抑制剂治疗的疾病中非常有用,包括与RET相关的疾病和紊乱。
  • HETEROCYCLIC COMPOUNDS AND USES THEREOF
    申请人:Ren Pingda
    公开号:US20120122838A1
    公开(公告)日:2012-05-17
    Compounds and pharmaceutical compositions that modulate kinase activity, including PI3 kinase activity, and compounds, pharmaceutical compositions, and methods of treatment of diseases and conditions associated with kinase activity, including PI3 kinase activity, are described herein.
    调节激酶活性的化合物和药物组合物,包括PI3激酶活性,以及与激酶活性相关的疾病和病况的化合物、药物组合物和治疗方法在此进行描述。
  • [EN] LIPOCATIONIC POLYMERS AND USES THEREOF<br/>[FR] POLYMÈRES LIPOCATIONIQUES ET LEURS UTILISATIONS
    申请人:UNIV TEXAS
    公开号:WO2016094342A1
    公开(公告)日:2016-06-16
    Polymers produced by ring opening polymerization which comprises an amino group that can be used in compositions to deliver a nucleic acid such as a miRNA or a siRNA. In some embodiments, compositions which comprise the polymers described herein and a nucleic acid are also provided herein. In some embodiments, these compositions are used to silence one or more genes in vivo or treat a disease or disorder.
    通过环氧聚合产生的聚合物,其中包含可以用于将核酸如miRNA或siRNA传递到组合物中的氨基团。在某些实施例中,还提供了包括所述聚合物和核酸的组合物。在某些实施例中,这些组合物被用于在体内沉默一个或多个基因或治疗疾病或紊乱。
  • CYCLOPROPYL COMPOUNDS
    申请人:Bueno Melendo Ana Belen
    公开号:US20100160395A1
    公开(公告)日:2010-06-24
    A compound of the formula: and pharmaceutical compositions for the treatment of diabetes.
    一个化学式为:的化合物和用于治疗糖尿病的药物组合物。
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