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2,5,7-Tri-t-butyl-tryptophan | 70561-70-5

中文名称
——
中文别名
——
英文名称
2,5,7-Tri-t-butyl-tryptophan
英文别名
L-Tryptophan, 2,5,7-tris(1,1-dimethylethyl)-;2-amino-3-(2,5,7-tritert-butyl-1H-indol-3-yl)propanoic acid
2,5,7-Tri-t-butyl-tryptophan化学式
CAS
70561-70-5
化学式
C23H36N2O2
mdl
——
分子量
372.551
InChiKey
IQMAPACPGQFJNG-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

物化性质

  • 沸点:
    500.1±50.0 °C(Predicted)
  • 密度:
    1.064±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.8
  • 重原子数:
    27
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.61
  • 拓扑面积:
    79.1
  • 氢给体数:
    3
  • 氢受体数:
    3

文献信息

  • OPIOID AGONIST PEPTIDES AND USES THEREOF
    申请人:Protagonist Therapeutics, Inc.
    公开号:US20190076400A1
    公开(公告)日:2019-03-14
    The invention is directed to opioid agonist peptides and their use.
    这项发明涉及阿片受体激动肽及其用途。
  • Bioactive peptides
    申请人:ALPHARMA AS
    公开号:US20030022821A1
    公开(公告)日:2003-01-30
    The present invention provides a modified lactoferrin peptide which is cytotoxic, 7 to 25 amino acids in length, with three or more cationic residues and which has one or more extra bulky and lipophilic amino acids as compared to the native lactoferrin sequence, as well as esters, amides, salts and cyclic derivatives thereof as well as methods of preparing such peptides, pharmaceutical compositions containing such peptides and use of the peptides as medicaments, particularly as antibacterials or anti-tumoural agents.
    本发明提供一种改性乳铁蛋白肽,其具有细胞毒性,长度为7至25个氨基酸,含有三个或更多阳离子残基,并且与天然乳铁蛋白序列相比,具有一个或多个额外的笨重和亲脂氨基酸,以及其酯、酰胺、盐和环状衍生物,以及制备这些肽的方法、含有这些肽的药物组合物和将这些肽用作药物的用途,特别是作为抗菌或抗肿瘤剂。
  • Inhibition of tumour growth
    申请人:Eliassen Tone Liv
    公开号:US20080019993A1
    公开(公告)日:2008-01-24
    The present invention provides a cytotoxic 7 to 25 mer peptide with three or more cationic residues which has one or more non-genetic bulky and lipophilic amino acids, as well as esters, amides, salts and cyclic derivatives thereof as well as methods of preparing the peptides, pharmaceutical compositions containing them and their use as medicaments, particularly as antibacterions or antitumoural agents. In a preferred aspect, the invention provides the use of said peptides in a method of inducing adaptive immunity against tumour growth or establishment in a subject, as well as the use of other lytic agents in a method of inducing adaptive immunity in a subject.
    本发明提供了一种细胞毒性的7至25个氨基酸残基的肽,其中含有三个或更多阳离子残基,其中含有一个或多个非遗传性的臃肿和亲脂性氨基酸,以及它们的酯类、酰胺、盐和环状衍生物,以及制备这些肽的方法、含有它们的药物组合物以及它们作为药物的用途,特别是作为抗菌或抗肿瘤剂。在一个优选方面,本发明提供了利用所述肽在主体中诱导适应性免疫反应以抑制肿瘤生长或建立的方法,以及利用其他溶解剂在主体中诱导适应性免疫反应的方法。
  • Antimicrobial Compounds and Formulations
    申请人:Svendsen John Sigurd
    公开号:US20120108520A1
    公开(公告)日:2012-05-03
    The invention relates to the use of a molecule comprising a backbone of 2 to 35 non-hydrogen atoms in length, having covalently attached thereto at least two bulky and lipophilic groups and having at least one more cationic than anionic moiety, in the manufacture of a medicament for destabilising microbial cell membranes and the use as a membrane acting antimicrobial agent of a molecule comprising a backbone of 2 to 35 non-hydrogen atoms in length, having covalently attached thereto a super bulky and lipophilic group comprising at least 9 non-hydrogen atoms and having at least two more cationic than anionic moieties and to methods of treatment involving such molecules, in particular peptides including peptide derivatives, and peptidomimetics.
    本发明涉及使用一种分子,其包含长度为2至35个非氢原子的骨架,并且至少连接有两个笨重和亲脂性基团,并且具有至少一个阳离子大于阴离子的基团,在制造破坏微生物细胞膜的药物方面使用该分子。另外,本发明还涉及使用一种分子作为膜作用抗微生物剂,该分子包括长度为2至35个非氢原子的骨架,并且共价连接有一个超大的、亲脂性的基团,包括至少9个非氢原子,并且具有至少两个阳离子大于阴离子的基团。本发明还涉及涉及这样的分子的治疗方法,特别是包括肽衍生物和肽类似物的肽。
  • INHIBITION OF TUMOR GROWTH
    申请人:Eliassen Liv Tone
    公开号:US20140037657A1
    公开(公告)日:2014-02-06
    The present invention provides a cytotoxic 7 to 25 mer peptide with three or more cationic residues which has one or more non-genetic bulky and lipophilic amino acids, as well as esters, amides, salts and cyclic derivatives thereof as well as methods of preparing the peptides, pharmaceutical compositions containing them and their use as medicaments, particularly as antibacterions or antitumoral agents. In a preferred aspect, the invention provides the use of said peptides in a method of inducing adaptive immunity against tumor growth or establishment in a subject, as well as the use of other lytic agents in a method of inducing adaptive immunity in a subject.
    本发明提供了一种具有三个或更多阳离子残基的细胞毒性7到25个氨基酸肽,其中具有一个或多个非遗传性臃肿和亲脂氨基酸,以及它们的酯,酰胺,盐和环状衍生物,以及制备肽的方法,含有它们的制药组合物以及它们作为药物的用途,特别是作为抗菌或抗肿瘤剂。在一个优选方面,本发明提供了在诱导受体中适应性免疫反应以抑制肿瘤生长或建立的方法中使用所述肽的用途,以及在诱导受体中适应性免疫反应的方法中使用其他溶解剂的用途。
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