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3-(Cyclohexylthio)-1-propanamine | 56216-09-2

中文名称
——
中文别名
——
英文名称
3-(Cyclohexylthio)-1-propanamine
英文别名
3-cyclohexylsulfanylpropan-1-amine
3-(Cyclohexylthio)-1-propanamine化学式
CAS
56216-09-2
化学式
C9H19NS
mdl
MFCD00093014
分子量
173.323
InChiKey
IYRIBRIAXGCUFF-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):
    2.1
  • 重原子数:
    11
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    51.3
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2930909090

SDS

SDS:30821b764819ce46da0b4bae5e8af097
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反应信息

  • 作为产物:
    参考文献:
    名称:
    β-肾上腺素能阻断剂。18.1-(芳氧基)-3-(芳硫基烷基氨基)丙-2-醇和1-取代的烷基硫氨基-3-(芳氧基)丙-2-醇。
    摘要:
    描述了1-(芳氧基)-3-(芳硫基烷基氨基)丙烷-2-醇和1-(烷基硫氨基)-和1-(芳烷基氨基)-3-(芳氧基)丙烷-2-醇的衍生物系列的合成。研究了这些化合物的β-肾上腺素受体阻滞特性以及对心脏β1受体的选择性作用。特别参考硫,亚砜和砜基团对β-肾上腺素受体阻断效能和选择性的影响,讨论了结构活性关系。
    DOI:
    10.1021/jm00206a010
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文献信息

  • Inhibitors of MshC and Homologs Thereof, and Methods of Identifying Same
    申请人:Fahey Robert C.
    公开号:US20100022509A1
    公开(公告)日:2010-01-28
    The present invention utilizes three families of bacterial enzymes, which play a key role in mycothiol biosynthesis. The three families are bacterial cysteine:glucosaminyl inositol ligases (MshC) with catalytic ligase activity for ligation of glucosaminyl inositol and cysteine, bacterial acetyl-CoA:Cys-GlcN-Ins acetyltransferases (MshD) with catalytic activity for addition of an acetyl group to Cys-GlcN-Ins and bacterial MshA glycosyltransferase with catalytic activity for production of GlcNAc-Ins. The invention provides methods for using the mycothiol biosynthesis ligases, acetyltransferases or glycosyltransferases in drug screening assays to determine compounds that inhibit activity. The invention also provides inhibitors of the production or activity of the enzymes of mycothiol biosynthesis, and use of the inhibitors for treating microbial infection.
    本发明利用三种细菌酶家族,它们在肌硫醇生物合成中起着关键作用。这三个家族是:具有催化配体活性的细菌半胱氨酸:葡萄糖胺酰肌醇连接酶(MshC),用于连接葡萄糖胺酰肌醇和半胱氨酸;具有催化活性的细菌乙酰辅酶A:半胱氨酸-GlcN-Ins乙酰转移酶(MshD),用于向Cys-GlcN-Ins添加乙酰基;以及具有催化活性的细菌MshA糖基转移酶,用于生产GlcNAc-Ins。本发明提供了使用肌硫醇生物合成连接酶、乙酰转移酶或糖基转移酶进行药物筛选测定的方法,以确定抑制活性的化合物。本发明还提供了肌硫醇生物合成酶的产生或活性的抑制剂,并将其用于治疗微生物感染。
  • COMPOSITION FOR OPTICAL MATERIAL
    申请人:MITSUBISHI GAS CHEMICAL COMPANY, INC.
    公开号:EP1426392A1
    公开(公告)日:2004-06-09
    The composition for optical materials of the present invention comprises a compound having in one molecule at least one structure represented by the following formula (1): wherein R1, R2, R3, R4, X, Y and n are as defined in the disclosure, an amine compound and an isocyanate compound. Resins obtained by curing the composition by polymerization are useful as well-balanced optical materials having a high impact resistance, a high refractive index and a sufficiently high Abbe's number.
    本发明的光学材料组合物包括在一个分子中至少具有下式(1)所代表的一种结构的化合物: 其中 R1、R2、R3、R4、X、Y 和 n 如公开资料中所定义;胺化合物和异氰酸酯化合物。通过聚合固化组合物得到的树脂可用作具有高抗冲击性、高折射率和足够高的阿贝数的均衡光学材料。
  • Use of small molecules for the treatment of clostridium difficile toxicity
    申请人:The Board of Trustees of the Leland Stanford Junior University
    公开号:US10172829B2
    公开(公告)日:2019-01-08
    Disclosed are methods and compositions for reducing toxicity associated with infection by Clostridium difficile by inhibiting Clostridium difficile toxin B (TcdB) and/or toxin A (TcdA). Such compounds include ebselen compounds, namely ebselen and its salts, ebselen functional analogues and ebselen structural analogues, as well as certain amide derivatives. This includes Formula I, e.g. 1-methyl-3-phenylpropylamine, Formula II, e.g., 2,2′-diselane-1,2-diylbis[N-(2,4-difluorophenyl)benzamide]; and Formula III, e.g. 2-(2-methoxy-5-methylphenyl)-1, 2-benzoselenazol-3-one. The present compositions may be comprised in a colon-retentive formulation that increases residence of and/or release of the compound in the area where the infection is active.
    所公开的是通过抑制艰难梭菌毒素B(TcdB)和/或毒素A(TcdA)来降低与艰难梭菌感染相关的毒性的方法和组合物。此类化合物包括依布硒化合物,即依布硒及其盐类、依布硒功能类似物和依布硒结构类似物,以及某些酰胺衍生物。这包括式 I,如 1-甲基-3-苯基丙胺;式 II,如 2,2′-二硒-1,2-二基双[N-(2,4-二氟苯基)苯甲酰胺];以及式 III,如 2-(2-甲氧基-5-甲基苯基)-1,2-苯并硒唑-3-酮。本组合物可包含在一种结肠保留制剂中,以增加化合物在感染活跃区域的停留和/或释放。
  • Composition for optical material
    申请人:——
    公开号:US20040147708A1
    公开(公告)日:2004-07-29
    The composition for optical materials of the present invention comprises a compound having in one molecule at least one structure represented by the following formula (1): 1 wherein R 1 , R 2 , R 3 , R 4 , X, Y and n are as defined in the disclosure, an amine compound and an isocyanate compound. Resins obtained by curing the composition by polymerization are useful as well-balanced optical materials having a high impact resistance, a high refractive index and a sufficiently high Abbe's number.
    本发明的光学材料组合物包括一种化合物,其一个分子中至少有一个结构由下式(1)表示: 1 其中 R 1 , R 2 , R 3 , R 4 X、Y 和 n 的定义、胺化合物和异氰酸酯化合物。通过聚合固化组合物得到的树脂可用作具有高抗冲击性、高折射率和足够高阿贝数的均衡光学材料。
  • USE OF SMALL MOLECULES FOR THE TREATMENT OF CLOSTRIDIUM DIFFICILE TOXICITY
    申请人:The Board of Trustees of the Leland Stanford Junior University
    公开号:EP3160465A1
    公开(公告)日:2017-05-03
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