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8-phenyl-2,6-dicarboxyethyl-4,4-difluoro-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene | 864969-59-5

中文名称
——
中文别名
——
英文名称
8-phenyl-2,6-dicarboxyethyl-4,4-difluoro-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene
英文别名
1,3,5,7-tetramethyl-2,6-bis(2-carboxyethyl)-8-phenyl-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene;bis-carboxylic acid (1,3,5,7-tetramethyl-2,6-bis(2-carboxyethyl)-8-phenyl-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene);PHBDP-COOH;3-[11-(2-Carboxyethyl)-2,2-difluoro-4,6,10,12-tetramethyl-8-phenyl-1-aza-3-azonia-2-boranuidatricyclo[7.3.0.03,7]dodeca-3,5,7,9,11-pentaen-5-yl]propanoic acid;3-[11-(2-carboxyethyl)-2,2-difluoro-4,6,10,12-tetramethyl-8-phenyl-1-aza-3-azonia-2-boranuidatricyclo[7.3.0.03,7]dodeca-3,5,7,9,11-pentaen-5-yl]propanoic acid
8-phenyl-2,6-dicarboxyethyl-4,4-difluoro-1,3,5,7-tetramethyl-4-bora-3a,4a-diaza-s-indacene化学式
CAS
864969-59-5
化学式
C25H27BF2N2O4
mdl
——
分子量
468.308
InChiKey
GKTCYUHNLQALFY-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):
    4.79
  • 重原子数:
    34
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.32
  • 拓扑面积:
    82.5
  • 氢给体数:
    2
  • 氢受体数:
    7

反应信息

点击查看最新优质反应信息

文献信息

  • In Vivo Fluorescence Imaging of Bone-Resorbing Osteoclasts
    作者:Toshiyuki Kowada、Junichi Kikuta、Atsuko Kubo、Masaru Ishii、Hiroki Maeda、Shin Mizukami、Kazuya Kikuchi
    DOI:10.1021/ja2064582
    日期:2011.11.9
    Osteoclasts are giant polykaryons responsible for bone resorption. Because an enhancement or loss of osteoclast function leads to bone diseases such as osteoporosis and osteopetrosis, real-time imaging of osteoclast activity in vivo can be of great help for the evaluation of drugs. Herein, pH-activatable chemical probes BAp-M and BAp-E have been developed for the detection of bone-resorbing osteoclasts in vivo. Their acid dissociation constants (pK(a)) were determined as 4.5 and 6.2 by fluorometry in various pH solutions. These plc values should be appropriate to perform selective imaging of bone-resorbing osteoclasts, because synthesized probes Cannot fluoresce intrinsically at physiological pH and the pH in the resorption pit is lowered to about 4.5. Furthermore, BAp-M and BAp-E have a bisphosphonate Moiety that enabled the probes to localize. on bone tissues. The hydroxyapatite (HA) binding assay in vitro was, therefore, performed to confirm the tight binding of the probes to the bone tissues. Our probes showed :intense fluorescence at pH values but no fluorescence signal under physiological pH conditions on HA. Finally, we applied the probes to in vivo imaging of osteoclasts by using intravital two-photon microscopy. As expected, the fluorescence signals of the probes were locally observed between; the osteoclasts and bone tissues, that is in resorption pits. These results indicate that our pH-activatable probe g will prove to be a powerful tool for the selective detection of bone-resorbing osteoclasts in vivo, because this is the first instance Where in vivo imaging has been conducted in a low-pH region created by bone-resorbing osteoclasts.
  • PH-SENSITIVE FLUORESCENT PROBE
    申请人:The University of Tokyo
    公开号:EP2098529B1
    公开(公告)日:2014-06-18
  • Targeted pH-dependent fluorescent activity-based cathepsin probes
    作者:Sascha Hoogendoorn、Kim L. Habets、Solène Passemard、Johan Kuiper、Gijsbert A. van der Marel、Bogdan I. Florea、Herman S. Overkleeft
    DOI:10.1039/c1cc12947c
    日期:——
    Bifunctional, pH-activatable BODIPY dyes were developed and incorporated in mannose cluster-containing activity-based probes for cysteine proteases. Mannose receptor-dependent uptake of the probes in dendritic cells, followed by trafficking to acidic cellular compartments resulted in fluorescence as seen by live-cell imaging, and subsequent cathepsin inhibition.
    研究人员开发了双功能、可激活 pH 值的 BODIPY 染料,并将其纳入含甘露糖簇的半胱氨酸蛋白酶活性探针中。树突状细胞依赖甘露糖受体摄取探针,然后将探针转运到酸性细胞区,通过活细胞成像看到荧光,随后抑制酪蛋白酶。
  • Kowada, Toshiyuki; Kikuta, Junichi; Kubo, Atsuko, Journal of the American Chemical Society
    作者:Kowada, Toshiyuki、Kikuta, Junichi、Kubo, Atsuko、Ishii, Masaru、Maeda, Hiroki、et al.
    DOI:——
    日期:——
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