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4-Nitro-2-toluolsulfonat | 121550-56-9

中文名称
——
中文别名
——
英文名称
4-Nitro-2-toluolsulfonat
英文别名
2-Methyl-4-nitrobenzenesulfonate
4-Nitro-2-toluolsulfonat化学式
CAS
121550-56-9
化学式
C7H6NO5S
mdl
——
分子量
216.194
InChiKey
XCSZUHHAYFILGO-UHFFFAOYSA-M
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):
    0.8
  • 重原子数:
    14
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    111
  • 氢给体数:
    0
  • 氢受体数:
    5

文献信息

  • [EN] PEPTIDE MACROCYCLES AGAINST ACINETOBACTER BAUMANNII<br/>[FR] MACROCYCLES PEPTIDIQUES CONTRE ACINETOBACTER BAUMANNII
    申请人:HOFFMANN LA ROCHE
    公开号:WO2017072062A1
    公开(公告)日:2017-05-04
    The present invention provides compounds of formula (I) wherein X1 to X8 and R1 to R8 are as described herein, as well as pharmaceutically acceptable salts thereof. Further the present invention is concerned with the manufacture of the compounds of formula (I), pharmaceutical compositions comprising them and their use as medicaments for the treatment of diseases and infections caused by Acinetobacter baumannii.
    本发明提供了式(I)的化合物,其中X1至X8和R1至R8如本文所述,以及其药学上可接受的盐。此外,本发明涉及制备式(I)的化合物,包括它们的药物组合物以及它们作为治疗由鲍曼不动杆菌引起的疾病和感染的药物的用途。
  • [EN] ANTI-BACTERIAL PEPTIDE MACROCYCLES AND USE THEREOF<br/>[FR] MACROCYCLES PEPTIDIQUES ANTIBACTÉRIENS ET LEUR UTILISATION
    申请人:HOFFMANN LA ROCHE
    公开号:WO2018189065A1
    公开(公告)日:2018-10-18
    The present invention relates to compounds of formula (I) wherein X1 to X8 and R1 to R8 are as described herein, as well as pharmaceutically acceptable salts thereof for the use in the treatment or prevention of infections and resulting diseases caused by Pseudomonas aeruginosa.
    本发明涉及式(I)的化合物,其中X1至X8和R1至R8如本文所述,以及其药学上可接受的盐,用于治疗或预防由绿假单胞菌引起的感染及其导致的疾病。
  • METHOD FOR PRODUCING PEPTIDE
    申请人:Kajihara Yasuhiro
    公开号:US20110172392A1
    公开(公告)日:2011-07-14
    The present invention provides a method for producing a peptide, characterized in that it comprises converting an —SH group of a peptide comprising an amino acid residue having the —SH group to an —OH group, wherein said method comprises the following steps (a) to (c): (a) allowing an —SH group in a peptide to react with a methylating agent to convert the —SH group to an —SMe group; (b) allowing the —SMe group obtained in the step (a) to react with a cyanizing agent to produce a reaction intermediate; and (c) converting the reaction intermediate obtained in the step (b) to a peptide comprising an amino acid residue having an —OH group under more basic conditions than the conditions in the step (b).
    本发明提供了一种制备肽的方法,其特征在于包括将具有—SH基的氨基酸残基的肽的—SH基转换为—OH基,其中所述方法包括以下步骤(a)至(c):(a)使肽中的—SH基与甲基化剂反应,将—SH基转换为—SMe基;(b)使步骤(a)中获得的—SMe基与化剂反应,生成反应中间体;以及(c)在比步骤(b)中的条件更为碱性的条件下将步骤(b)中获得的反应中间体转化为具有—OH基的氨基酸残基的肽。
  • GLYCOSYLATED POLYPEPTIDE AND PHARMACEUTICAL COMPOSITION CONTAINING SAME
    申请人:GLYTECH, INC.
    公开号:US20140369964A1
    公开(公告)日:2014-12-18
    The object of the present invention is to provide a glycosylated polypeptide having uniform sugar chain structure which has interferon β activity. It was found that a glycosylated polypeptide having uniform sugar chain structure as well as having interferon β activity can be prepared by a method comprising a step of synthesizing a glycosylated peptide fragment and at least two peptide fragments and a step of linking the glycosylated peptide fragment and the at least two peptide fragments.
    本发明的目的是提供一种具有干扰素β活性的糖基化多肽,其具有均匀的糖链结构。发现通过合成糖基化肽段和至少两个肽段的方法以及连接糖基化肽段和至少两个肽段的步骤,可以制备具有均匀糖链结构和干扰素β活性的糖基化多肽
  • SORBIC ACID AND DERIVATIVES THEREOF TO ENHANCE THE ACTIVITY OF A NEUROPHARMACEUTICAL
    申请人:Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center
    公开号:EP3006023A1
    公开(公告)日:2016-04-13
    Methods and compositions are provided for treating neuropsychiatric disorders such as schizophrenia, depression, attention deficit disorder, mild cognitive impairment, dementia, and bipolar disorder. The methods entail administering to a patient diagnosed as having a neuropsychiatric disorder (e.g., schizophrenia, depression, attention deficit disorder, mild cognitive impairment, dementia bipolar disorder, etc.) or as at risk for a neuropsychiatric disorder a benzoic acid, benzoic acid salt, and/or benzoic acid derivative, and/or a sorbic acid, sorbic acid salt, and/or sorbic acid derivative, in combination with a neuropharmacological agent (e.g., an antipsychotic, an antidepressant, medications for attention deficit and hyperactivity disorder, cognitive impairment, or dementia, etc.) where the benzoic acid, benzoic acid salt, or benzoic acid derivative, and/or a sorbic acid, sorbic acid salt, and/or sorbic acid derivative, is in an amount sufficient to increase the efficacy of the neuropharmacological agent.
    本文提供了治疗神经精神疾病(如精神分裂症、抑郁症、注意力缺陷障碍、轻度认知障碍、痴呆症和双相情感障碍)的方法和组合物。这些方法需要给被诊断为患有神经精神障碍(如精神分裂症、抑郁症、注意力缺陷障碍、轻度认知障碍、痴呆症、双相情感障碍等)或有神经精神障碍风险的患者施用苯甲酸苯甲酸盐和/或苯甲酸生物和/或山梨酸山梨酸盐和/或山梨酸生物,并与神经药剂(如抗精神病药抗精神病药抗精神病药抗精神病药)结合使用、苯甲酸苯甲酸盐或苯甲酸生物和/或山梨酸山梨酸盐和/或山梨酸生物的用量足以提高神经药剂的药效。
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同类化合物

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