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5-(氨基甲基)荧光素盐酸盐 | 141749-41-9

中文名称
5-(氨基甲基)荧光素盐酸盐
中文别名
——
英文名称
5-(Aminomethyl)-3',6'-dihydroxy-3H-spiro[isobenzofuran-1,9'-xanthen]-3-one hydrochloride
英文别名
6-(aminomethyl)-3',6'-dihydroxyspiro[2-benzofuran-3,9'-xanthene]-1-one;hydrochloride
5-(氨基甲基)荧光素盐酸盐化学式
CAS
141749-41-9
化学式
C21H16ClNO5
mdl
——
分子量
397.8
InChiKey
DRSLEJZHHOQFSF-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):
    3.55
  • 重原子数:
    28
  • 可旋转键数:
    1
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    102
  • 氢给体数:
    4
  • 氢受体数:
    6

文献信息

  • DERIVATIVE OF HYALURONIC ACID MODIFIED WITH AMINO-CARBOXYLIC ACID
    申请人:Yasugi Tomoko
    公开号:US20130338352A1
    公开(公告)日:2013-12-19
    The present invention provides a hyaluronic acid derivative comprising disaccharide units of Formula (I), and a hyaluronic acid derivative/drug conjugate wherein one or more drugs are conjugated to the hyaluronic acid derivative.
    本发明提供了一种透明质酸衍生物,其中包括式(I)的二糖单元,以及一种透明质酸衍生物/药物结合物,其中一个或多个药物与透明质酸衍生物结合。
  • Immunoassay reagents and method for determining cyclosporine
    申请人:ABBOTT LABORATORIES
    公开号:EP0473961A2
    公开(公告)日:1992-03-11
    Cyclosporine derivatives useful as detectable tracer compounds for the immunoassay determination of cyclosporine are disclosed. The cyclosporine derivatives comprise a detectable moiety coupled to the amino acid at the first position (MeBmt) in cyclosporine, the second position (Abu) in cyclosporine, the third position (Sar) in cyclosporine, the eighth position (D-Ala) in cyclosporine, or the tenth position (MeLeu) in cyclosporine. A preferred cyclosporine derivative comprises a fluorescent moiety coupled to the hydroxyl group of the amino acid at the first position in cyclosporine, and is especially useful for the fluorescent polarization immunoassay deterimination of cyclosporine. A fluorescent polarization immunoassay method and test kit are also disclosed.
    本发明公开了可用作免疫测定环孢素的可检测示踪化合物的环孢素生物。这些环孢素生物包括与环孢素第一位(MeBmt)、环孢素第二位(Abu)、环孢素第三位(Sar)、环孢素第八位(D-Ala)或环孢素第十位(MeLeu)氨基酸偶联的可检测分子。一种优选的环孢素生物包含一个与环孢素中第一位氨基酸的羟基偶联的荧光分子,特别适用于荧光偏振免疫测定环孢素。还公开了一种荧光偏振免疫测定方法和检测试剂盒。
  • Quinidine immunoassay and reagents
    申请人:F. HOFFMANN-LA ROCHE AG
    公开号:EP0745602A1
    公开(公告)日:1996-12-04
    The invention provides: novel quinidine derivatives of formula wherein L is a a C1-C10 hydrocarbon linking group which may be straight or branched chain, saturated or unsaturated, and may include from 0 to 3 heteroatoms; and F is a functional group selected from the group consisting of amino, carboxyl, sulfhydryl, imino, and maleimide, haptens, immunogens, antibodies and tracers produced from those novel derivatives, and an improved quinidine fluorescence polarization immunoassay utilizing those antibodies and tracers.
    本发明提供了 式中 L 为 C1-C10 烃连接基团,可以是直链或支链、饱和或不饱和,并可包括 0 至 3 个杂原子;F 为官能团,选自由基、羧基、巯基、亚基和马来酰亚胺组成的组;由这些新型衍生物制备的触媒、免疫原、抗体和示踪剂;以及利用这些抗体和示踪剂的改进型奎尼丁荧光偏振免疫分析法。
  • 8-ARM POLYETHYLENE GLYCOL DERIVATIVE, MANUFACTURING METHOD AND MODIFIED BIO-RELATED SUBSTANCE THEREBY
    申请人:Xiamen Sinopeg Biotech Co., Ltd.
    公开号:EP3315531A1
    公开(公告)日:2018-05-02
    Disclosed are an 8-arm polyethylene glycol (PEG) derivative (formula 1), manufacturing method and modified bio-related substance thereby, wherein a tetravalent group U and four trivalent groups Ec form a highly symmetric octavalent central structure CORE0 together, Lc connects the octavalent center to eight PEG arms having polydiversity or monodiversity and having n1-n8 as the degrees of polymerization thereof. The terminal of one PEG chain is connected to at least one functional group F (k ≥ 1), and said PEG chain and F can be directly connected (g = 0) or connected with a divalent linking group L0 connected with a terminal branched group G (g = 1) therebetween. The latter provides more reacting sites to combine more pharmaceutical molecules, thereby increasing the drug loading capacity. The near-center symmetric structure of the derivative allows more precise control over the molecular weight during large-scale production, thereby facilitating acquisition of a product having a narrower molecular weight distribution. A bio-related substance modified thereby has a more uniform and controllable performance.
    本发明公开了一种 8 臂聚乙二醇(PEG)衍生物(式 1)、其制造方法和改性生物相关物质,其中一个四价基团 U 和四个三价基团 Ec 共同形成一个高度对称的八价中心结构 CORE0,Lc 将八价中心连接到八个 PEG 臂上,这些 PEG 臂具有多元性或单元性,其聚合度为 n1-n8。一条 PEG 链的末端与至少一个官能团 F(k ≥ 1)相连,所述 PEG 链和 F 可以直接相连(g = 0),也可以通过二价连接基 L0 与中间的末端支化基 G(g = 1)相连。后者提供了更多的反应位点,可以结合更多的药物分子,从而提高药物负载能力。衍生物的近中心对称结构可以在大规模生产过程中更精确地控制分子量,从而有利于获得分子量分布更窄的产品。由此改性的生物相关物质具有更均匀、更可控的性能。
  • Eight-arm polyethylene glycol derivative, production method therefor, and modified bio-related substance thereof
    申请人:XIAMEN SINOPEG BIOTECH CO., LTD.
    公开号:US10434182B2
    公开(公告)日:2019-10-08
    Disclosed are an eight-arm polyethylene glycol (PEG) derivative (formula I), production method therefor and modified bio-related substance thereby. Wherein, one tetravalent group U together with four trivalent groups Ec form a highly symmetrical octavalent group CORE0; Lc connects the octavalent group to eight PEG chains having polydispersity or monodispersity and having n1 to n8 as the degree of polymerization thereof; the terminal of one PEG chain is connected to at least one functional group F (k≥1); said PEG chain and F therebetween can be directly connected (g=0) or be indirectly connected via a linking group L0 to a terminal end-branching group G (g=1); the latter provides more reactive sites for binding more drug molecules and increases the drug loading. The eight-arm polyethylene glycol derivative has a centrosymmetric or approximately centrosymmetric structure, and leads to more precise control of the molecular weight in large-scale production and much narrower distribution of molecular weight for products. The modified bio-related substance thereby has a more uniform and controllable performance.
    本发明公开了一种八臂聚乙二醇(PEG)衍生物(式 I)、其生产方法及其改性生物相关物质。其中,一个四价基团 U 与四个三价基团 Ec 形成一个高度对称的八价基团 CORE0;Lc 将八价基团连接到八条具有多分散性或单分散性且聚合度为 n1 至 n8 的 PEG 链上;一条 PEG 链的末端与至少一个官能团 F 连接(k≥1);所述 PEG 链和 F 之间可以直接连接(g=0),也可以通过连接基团 L0 与末端支化基团 G 间接连接(g=1);后者提供了更多的反应位点,可以结合更多的药物分子,增加药物负载量。八臂聚乙二醇衍生物具有中心对称或近似中心对称结构,因此在大规模生产中可以更精确地控制分子量,产品的分子量分布也更窄。因此,改性生物相关物质的性能更均匀、更可控。
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