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1-Amino-6-hydroxy-16--7.10-dioxo-6,11-diaza-hexadecan | 252325-60-3

中文名称
——
中文别名
——
英文名称
1-Amino-6-hydroxy-16--7.10-dioxo-6,11-diaza-hexadecan
英文别名
Deferoxamine mesilate impurity B [EP impurity];N-[5-[acetyl(hydroxy)amino]pentyl]-N'-(5-aminopentyl)-N'-hydroxybutanediamide
1-Amino-6-hydroxy-16-<N-acetyl-hydroxylamino>-7.10-dioxo-6,11-diaza-hexadecan化学式
CAS
252325-60-3
化学式
C16H32N4O5
mdl
——
分子量
360.454
InChiKey
RSSRKKMWVNCQBZ-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):
    -1.4
  • 重原子数:
    25
  • 可旋转键数:
    14
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.81
  • 拓扑面积:
    136
  • 氢给体数:
    4
  • 氢受体数:
    6

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Reverse Biosynthesis: Generating Combinatorial Pools of Drug Leads from Enzyme-Mediated Fragmentation of Natural Products
    作者:Tomas Richardson-Sanchez、William Tieu、Rachel Codd
    DOI:10.1002/cbic.201600636
    日期:2017.2.16
    desferrioxamine B (1) gave a pool of catabolites; subsequent derivatisation yielded a 5‐lipoxygenase inhibitor. This top‐down approach to generate new drug leads from a natural product, “reverse biosynthesis”, provides a new perspective on natural products as a resource for drug discovery.
    建设性破坏:天然产物去铁草胺B(1)的酶介导裂解产生大量的分解代谢产物。随后的衍生化产生了5-脂氧合酶抑制剂。这种从天然产物“逆向生物合成”产生新药线索的自上而下的方法为将天然产物作为发现药物的资源提供了新的视角。
  • ZIRCONIUM-RADIOLABELED, CYSTEINE ENGINEERED ANTIBODY CONJUGATES
    申请人:Gill Herman
    公开号:US20100111856A1
    公开(公告)日:2010-05-06
    Antibodies are engineered by replacing one or more amino acids of a parent antibody with non cross-linked, highly reactive cysteine amino acids. Antibody fragments may also be engineered with one or more cysteine amino acids to form cysteine engineered antibody fragments (ThioFab). Methods of design, preparation, screening, and selection of the cysteine engineered antibodies are provided. Cysteine engineered antibodies (Ab) are conjugated with one or more zirconium complex (Z) labels through a linker (L) to form cysteine engineered zirconium-labeled antibody conjugates having Formula I: Ab-(L-Z) p I where p is 1 to 4. Imaging methods and diagnostic uses for zirconium-radiolabeled, cysteine engineered antibody conjugate compositions are disclosed.
    抗体是通过将一个或多个亲缘抗体的氨基酸替换为非交联、高反应性的半胱氨酸氨基酸来设计的。抗体片段也可以通过引入一个或多个半胱氨酸氨基酸来设计半胱氨酸工程抗体片段(ThioFab)。提供了设计、制备、筛选和选择半胱氨酸工程抗体的方法。半胱氨酸工程抗体(Ab)通过连接剂(L)与一个或多个锆配合物(Z)标记结合,形成具有公式I的半胱氨酸工程锆标记抗体结合物:Ab-(L-Z)pI,其中p为1至4。揭示了锆放射标记、半胱氨酸工程抗体结合物组合物的成像方法和诊断用途。
  • Stoffwechselprodukte von Mikroorganismen 49. Mitteilung. Die Ferrioxamine A1, A2 und D2
    作者:W. Keller-Schierlein、P. Mertens、V. Prelog、A. Walser
    DOI:10.1002/hlca.19650480407
    日期:——
    AbstractThe structures of the ferrioxamines A1, A2, and D2, minor components of the sideramine mixtures from cultures of Streptomyces, have been determined by degradation and, in part, by synthesis. Whereas the previously investigated ferrioxamines B, D1, E, and G contain but a single basic component, 1‐amino‐5‐hydroxylaminopentane, the ferrioxamines A1, A2, and D2 contain in addition to this base its lower homologue, 1‐amino‐4‐hydroxylamino‐butane.
  • USE OF MITOCHONDRIA-TARGETED ELECTRON SCAVENGERS AS ANTI-INFLAMMATORY AGENTS
    申请人:Fink Mitchell P.
    公开号:US20090042808A1
    公开(公告)日:2009-02-12
    Provided herein are methods for using mitochondria-targeted electron scavengers as anti-inflammatory agents. The mitochondria-targeted electron scavenger comprises a free radical-scavenging group covalently linked to a mitochondria-targeting group derived from a hemigramicidin moiety. The mitochondria-targeted electron scavenger can be used to treat medical conditions associated with acute or chronic inflammation.
  • BICYCLIC PEPTIDE LIGANDS WITH DETECTABLE MOIETIES AND USES THEREOF
    申请人:BicycleRD Limited
    公开号:US20210079045A1
    公开(公告)日:2021-03-18
    The present invention provides compounds, compositions thereof, and methods of using the same.
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