摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

6-azaniumyl-2-[(2-azaniumyl-3-carboxylatopropanoyl)amino]hexanoate

中文名称
——
中文别名
——
英文名称
6-azaniumyl-2-[(2-azaniumyl-3-carboxylatopropanoyl)amino]hexanoate
英文别名
——
6-azaniumyl-2-[(2-azaniumyl-3-carboxylatopropanoyl)amino]hexanoate化学式
CAS
——
化学式
C10H19N3O5
mdl
——
分子量
261.28
InChiKey
OAMLVOVXNKILLQ-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):
    -5.3
  • 重原子数:
    18
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.7
  • 拓扑面积:
    165
  • 氢给体数:
    3
  • 氢受体数:
    5

文献信息

  • MICROFLUIDIC PROTEIN CRYSTALLOGRAPHY
    申请人:Hansen Carl L.
    公开号:US20110306522A1
    公开(公告)日:2011-12-15
    The use of microfluidic structures enables high throughput screening of protein crystallization. In one embodiment, an integrated combinatoric mixing chip allows for precise metering of reagents to rapidly create a large number of potential crystallization conditions, with possible crystal formations observed on chip. In an alternative embodiment, the microfluidic structures may be utilized to explore phase space conditions of a particular protein crystallizing agent combination, thereby identifying promising conditions and allowing for subsequent focused attempts to obtain crystal growth.
    微流控结构的使用使得蛋白质结晶的高通量筛选成为可能。在一种实施方式中,集成的组合混合芯片允许精确计量试剂,以快速创建大量可能的结晶条件,并在芯片上观察到可能的晶体形成。在另一种实施方式中,微流控结构可以用于探索特定蛋白质结晶剂组合的相空间条件,从而确定有前途的条件,并允许随后集中尝试获得晶体生长。
  • HIGH THROUGHPUT SCREENING OF CRYSTALLIZATION OF MATERIALS
    申请人:California Institute of Technology
    公开号:US20140041727A1
    公开(公告)日:2014-02-13
    High throughput screening of crystallization of a target material is accomplished by simultaneously introducing a solution of the target material into a plurality of chambers of a microfabricated fluidic device. The microfabricated fluidic device is then manipulated to vary the solution condition in the chambers, thereby simultaneously providing a large number of crystallization environments. Control over changed solution conditions may result from a variety of techniques, including but not limited to metering volumes of crystallizing agent into the chamber by volume exclusion, by entrapment of volumes of crystallizing agent determined by the dimensions of the microfabricated structure, or by cross-channel injection of sample and crystallizing agent into an array of junctions defined by intersecting orthogonal flow channels.
    通过将目标材料的溶液同时引入微型流体装置的多个腔室中,实现对目标材料结晶的高通量筛选。然后,操纵微型流体装置来改变腔室中的溶液条件,从而同时提供大量的结晶环境。改变溶液条件的控制可以采用各种技术,包括但不限于通过体积排斥将结晶剂体积计量到腔室中,通过微型加工结构的尺寸确定结晶剂体积的困扰,或通过交叉正交流道定义的连接点阵列中的样品和结晶剂的交叉通道注入。
  • AMINO ACID-, PEPTIDE- AN POLYPEPTIDE-LIPIDS, ISOMERS, COMPOSITIONS, AN USES THEREOF
    申请人:Massachusetts Institute Of Technology
    公开号:EP4074694A1
    公开(公告)日:2022-10-19
    Described herein are compounds and compositions characterized, in certain embodiments, by conjugation of various groups, such as lipophilic groups, to an amino or amide group of an amino acid, a linear or cyclic peptide, a linear or cyclic polypeptide, or structural isomer thereof, to provide compounds of the present invention, collectively referred to herein as "APPLs". Such APPLs are deemed useful for a variety of applications, such as, for example, improved nucleotide delivery. Exemplary APPLs include, but are not limited to, compounds of Formula (I), (II), (III), (IV), (V), and (VI), and salts thereof, as described herein: wherein m, n, p, R', R1, R2, R3, R4, R5, R8, Z, W, Y, and Z are as defined herein.
    本文描述的化合物和组合物,在某些实施方案中,通过将各种基团(如亲油基团)与氨基酸的氨基或酰胺基团、线性或环状肽、线性或环状多肽或其结构异构体共轭,以提供本发明的化合物,本文统称为 "APPLs"。此类 APPL 被认为可用于多种应用,例如,改善核苷酸递送。示例性 APPL 包括但不限于本文所述的式 (I)、(II)、(III)、(IV)、(V) 和 (VI) 及其盐类化合物: 其中 m、n、p、R'、R1、R2、R3、R4、R5、R8、Z、W、Y 和 Z 如本文所定义。
  • Amino acid-, peptide- and polypeptide-lipids, isomers, compositions, and uses thereof
    申请人:Massachusetts Institute of Technology
    公开号:US10682374B2
    公开(公告)日:2020-06-16
    Described herein are compounds and compositions characterized, in certain embodiments, by conjugation of various groups, such as lipophilic groups, to an amino or amide group of an amino acid, a linear or cyclic peptide, a linear or cyclic polypeptide, or structural isomer thereof, to provide compounds of the present invention, collectively referred to herein as “APPLs”. Such APPLs are deemed useful for a variety of applications, such as, for example, improved nucleotide delivery. Exemplary APPLs include, but are not limited to, compounds of Formula (I), (II), (III), (IV), (V), and (VI), and salts thereof, as described herein: wherein m, n, p, R′, R1, R2, R3, R4, R5, R8, Z, W, Y, and Z are as defined herein.
    本文描述的化合物和组合物,在某些实施方案中,通过将各种基团(如亲油基团)与氨基酸的氨基或酰胺基团、线性或环状肽、线性或环状多肽或其结构异构体共轭,以提供本发明的化合物,本文统称为 "APPLs"。此类 APPL 被认为可用于多种应用,例如,改善核苷酸递送。示例性 APPL 包括但不限于本文所述的式 (I)、(II)、(III)、(IV)、(V) 和 (VI) 及其盐类化合物: 其中 m、n、p、R′、R1、R2、R3、R4、R5、R8、Z、W、Y 和 Z 如本文所定义。
  • High throughput screening of crystallization materials
    申请人:California Institute of Technology, A California Corporation
    公开号:US20030061687A1
    公开(公告)日:2003-04-03
    High throughput screening of crystallization of a target material is accomplished by simultaneously introducing a solution of the target material into a plurality of chambers of a microfabricated fluidic device. The microfabricated fluidic device is then manipulated to vary the solution condition in the chambers, thereby simultaneously providing a large number of crystallization environments. Control over changed solution conditions may result from a variety of techniques, including but not limited to metering volumes of crystallizing agent into the chamber by volume exclusion, by entrapment of volumes of crystallizing agent determined by the dimensions of the microfabricated structure, or by cross-channel injection of sample and crystallizing agent into an array of junctions defined by intersecting orthogonal flow channels.
    目标材料结晶的高通量筛选是通过将目标材料溶液同时引入微型流体设备的多个腔室来实现的。然后操纵微型流体设备来改变腔室中的溶液条件,从而同时提供大量的结晶环境。对变化的溶液条件的控制可采用多种技术,包括但不限于通过体积排阻将结晶剂计量到腔室中,根据微制造结构的尺寸决定结晶剂的体积,或将样品和结晶剂跨通道注入由相交的正交流道定义的结点阵列中。
查看更多

同类化合物

(甲基3-(二甲基氨基)-2-苯基-2H-azirene-2-羧酸乙酯) (±)-盐酸氯吡格雷 (±)-丙酰肉碱氯化物 (d(CH2)51,Tyr(Me)2,Arg8)-血管加压素 (S)-(+)-α-氨基-4-羧基-2-甲基苯乙酸 (S)-阿拉考特盐酸盐 (S)-赖诺普利-d5钠 (S)-2-氨基-5-氧代己酸,氢溴酸盐 (S)-2-[3-[(1R,2R)-2-(二丙基氨基)环己基]硫脲基]-N-异丙基-3,3-二甲基丁酰胺 (S)-1-(4-氨基氧基乙酰胺基苄基)乙二胺四乙酸 (S)-1-[N-[3-苯基-1-[(苯基甲氧基)羰基]丙基]-L-丙氨酰基]-L-脯氨酸 (R)-乙基N-甲酰基-N-(1-苯乙基)甘氨酸 (R)-丙酰肉碱-d3氯化物 (R)-4-N-Cbz-哌嗪-2-甲酸甲酯 (R)-3-氨基-2-苄基丙酸盐酸盐 (R)-1-(3-溴-2-甲基-1-氧丙基)-L-脯氨酸 (N-[(苄氧基)羰基]丙氨酰-N〜5〜-(diaminomethylidene)鸟氨酸) (6-氯-2-吲哚基甲基)乙酰氨基丙二酸二乙酯 (4R)-N-亚硝基噻唑烷-4-羧酸 (3R)-1-噻-4-氮杂螺[4.4]壬烷-3-羧酸 (3-硝基-1H-1,2,4-三唑-1-基)乙酸乙酯 (2S,3S,5S)-2-氨基-3-羟基-1,6-二苯己烷-5-N-氨基甲酰基-L-缬氨酸 (2S,3S)-3-((S)-1-((1-(4-氟苯基)-1H-1,2,3-三唑-4-基)-甲基氨基)-1-氧-3-(噻唑-4-基)丙-2-基氨基甲酰基)-环氧乙烷-2-羧酸 (2S)-2,6-二氨基-N-[4-(5-氟-1,3-苯并噻唑-2-基)-2-甲基苯基]己酰胺二盐酸盐 (2S)-2-氨基-3-甲基-N-2-吡啶基丁酰胺 (2S)-2-氨基-3,3-二甲基-N-(苯基甲基)丁酰胺, (2S,4R)-1-((S)-2-氨基-3,3-二甲基丁酰基)-4-羟基-N-(4-(4-甲基噻唑-5-基)苄基)吡咯烷-2-甲酰胺盐酸盐 (2R,3'S)苯那普利叔丁基酯d5 (2R)-2-氨基-3,3-二甲基-N-(苯甲基)丁酰胺 (2-氯丙烯基)草酰氯 (1S,3S,5S)-2-Boc-2-氮杂双环[3.1.0]己烷-3-羧酸 (1R,4R,5S,6R)-4-氨基-2-氧杂双环[3.1.0]己烷-4,6-二羧酸 齐特巴坦 齐德巴坦钠盐 齐墩果-12-烯-28-酸,2,3-二羟基-,苯基甲基酯,(2a,3a)- 齐墩果-12-烯-28-酸,2,3-二羟基-,羧基甲基酯,(2a,3b)-(9CI) 黄酮-8-乙酸二甲氨基乙基酯 黄荧菌素 黄体生成激素释放激素 (1-5) 酰肼 黄体瑞林 麦醇溶蛋白 麦角硫因 麦芽聚糖六乙酸酯 麦根酸 麦撒奎 鹅膏氨酸 鹅膏氨酸 鸦胆子酸A甲酯 鸦胆子酸A 鸟氨酸缩合物