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(S)-t-butyl 3-(4-(4-(t-butoxycarbonyl(4-methylpyridin-2-yl)amino)butoxy)-3-nitrophenyl)-2-(3-(trifluoromethyl)phenylsulfonamido)propanoate | 1197191-44-8

中文名称
——
中文别名
——
英文名称
(S)-t-butyl 3-(4-(4-(t-butoxycarbonyl(4-methylpyridin-2-yl)amino)butoxy)-3-nitrophenyl)-2-(3-(trifluoromethyl)phenylsulfonamido)propanoate
英文别名
tert-butyl (2S)-3-(3-nitro-4-[(4-oxopentyl)oxy]phenyl)-2-([3-(trifluoromethyl)benzene]sulfonamido)propanoate;tert-butyl (2S)-3-[3-nitro-4-(4-oxopentoxy)phenyl]-2-[[3-(trifluoromethyl)phenyl]sulfonylamino]propanoate
(S)-t-butyl 3-(4-(4-(t-butoxycarbonyl(4-methylpyridin-2-yl)amino)butoxy)-3-nitrophenyl)-2-(3-(trifluoromethyl)phenylsulfonamido)propanoate化学式
CAS
1197191-44-8
化学式
C25H29F3N2O8S
mdl
——
分子量
574.575
InChiKey
RMPBZLCPKWCVHB-FQEVSTJZSA-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):
    4.5
  • 重原子数:
    39
  • 可旋转键数:
    13
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    153
  • 氢给体数:
    1
  • 氢受体数:
    12

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2-氨基-3-吡啶甲醛(S)-t-butyl 3-(4-(4-(t-butoxycarbonyl(4-methylpyridin-2-yl)amino)butoxy)-3-nitrophenyl)-2-(3-(trifluoromethyl)phenylsulfonamido)propanoateL-脯氨酸 作用下, 以 乙醇 为溶剂, 反应 48.0h, 以55%的产率得到(S)-t-butyl 3-(4-(3-[1,8]naphthyridin-2-ylpropoxy)-3-nitrophenyl)-2-(3-(trifluoromethyl)phenylsulfonamido)propanoate
    参考文献:
    名称:
    Ultrasmall particle of iron oxide—RGD peptidomimetic conjugate: synthesis and characterisation
    摘要:
    Ultrasmall particles of iron oxide (USPIOs) coated with 3,3'-bis(phosphonate) propionic acid were covalently coupled to a home-made Arg-Gly-Asp (RGD) peptidomimetic molecule via a short oligoethyleneglycol (OEG) spacer. The conjugation rate was measured by X-ray photoelectron spectroscopy (XPS). The particle size and magnetic characteristics were kept. Our novel conjugate targeted efficiently Jurkat cells (increase of 229% vs the control). (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.01.150
  • 作为产物:
    描述:
    5-羟基-2-戊酮 、 t-butyl meta-nitro-N-[3-(trifluoromethyl)phenylsulfonyl]-L-tyrosinate 在 三苯基膦偶氮二甲酸二乙酯 作用下, 以 四氢呋喃 为溶剂, 反应 17.0h, 以51%的产率得到(S)-t-butyl 3-(4-(4-(t-butoxycarbonyl(4-methylpyridin-2-yl)amino)butoxy)-3-nitrophenyl)-2-(3-(trifluoromethyl)phenylsulfonamido)propanoate
    参考文献:
    名称:
    Ultrasmall particle of iron oxide—RGD peptidomimetic conjugate: synthesis and characterisation
    摘要:
    Ultrasmall particles of iron oxide (USPIOs) coated with 3,3'-bis(phosphonate) propionic acid were covalently coupled to a home-made Arg-Gly-Asp (RGD) peptidomimetic molecule via a short oligoethyleneglycol (OEG) spacer. The conjugation rate was measured by X-ray photoelectron spectroscopy (XPS). The particle size and magnetic characteristics were kept. Our novel conjugate targeted efficiently Jurkat cells (increase of 229% vs the control). (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.01.150
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文献信息

  • α<sub>v</sub>β<sub>3</sub> Integrin-Targeting Arg-Gly-Asp (RGD) Peptidomimetics Containing Oligoethylene Glycol (OEG) Spacers
    作者:Vincent Rerat、Georges Dive、Alex A. Cordi、Gordon C. Tucker、Reine Bareille、Joëlle Amédée、Laurence Bordenave、Jacqueline Marchand-Brynaert
    DOI:10.1021/jm901133z
    日期:2009.11.26
    RGD peptides are used in biomaterials science for surface modifications with a view to elicit selective cellular responses. Our objective is to replace peptides by small peptidomimetics acting similarly. We designed novel molecules targeting alpha(v)beta(3) integrin and featuring spacer-arms (for surface grafting), which do not disturb the biological activity, from (L) N-(3-(trifluoromethyl)benzenesulfonyl) tyrosine used as scaffold. Various Arg-mimics were fixed on the phenol function, and the ortho position was used for the Coupling of OEG spacers. All peptidomimetics were active in the nM range in a binding test toward human alpha(v)beta(3) integrin (IC50 = 0.1 to 1.7 nM) and selective versus platelet integrin alpha(IIb)beta(3) Selected compounds revealed excellent ability to inhibit bone cells adhesion on vitronectin. Modeling and docking studies were performed for comparing the most active RGD peptidomimetic to cilengitide, i.e., cyclo-[RGDfN(Me)V]-. Lastly, the adhesion of endothelial cells on a cultivation support grafted with RGD peptidomimetics was significantly improved.
  • Ultrasmall particle of iron oxide—RGD peptidomimetic conjugate: synthesis and characterisation
    作者:Vincent Rerat、Sophie Laurent、Carmen Burtéa、Benoît Driesschaert、Vincent Pourcelle、Luce Vander Elst、Robert N. Muller、Jacqueline Marchand-Brynaert
    DOI:10.1016/j.bmcl.2010.01.150
    日期:2010.3
    Ultrasmall particles of iron oxide (USPIOs) coated with 3,3'-bis(phosphonate) propionic acid were covalently coupled to a home-made Arg-Gly-Asp (RGD) peptidomimetic molecule via a short oligoethyleneglycol (OEG) spacer. The conjugation rate was measured by X-ray photoelectron spectroscopy (XPS). The particle size and magnetic characteristics were kept. Our novel conjugate targeted efficiently Jurkat cells (increase of 229% vs the control). (C) 2010 Elsevier Ltd. All rights reserved.
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