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(1',3',3'-Trimethylspiro[benzo[f][1,4]benzoxazine-3,2'-indole]-6'-yl)methanol | 849114-06-3

中文名称
——
中文别名
——
英文名称
(1',3',3'-Trimethylspiro[benzo[f][1,4]benzoxazine-3,2'-indole]-6'-yl)methanol
英文别名
——
(1',3',3'-Trimethylspiro[benzo[f][1,4]benzoxazine-3,2'-indole]-6'-yl)methanol化学式
CAS
849114-06-3
化学式
C23H22N2O2
mdl
——
分子量
358.44
InChiKey
QJEZIEZNTUZSSU-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):
    4.2
  • 重原子数:
    27
  • 可旋转键数:
    1
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    45.1
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    (1',3',3'-Trimethylspiro[benzo[f][1,4]benzoxazine-3,2'-indole]-6'-yl)methanol四溴化碳三苯基膦 作用下, 以 四氢呋喃 为溶剂, 以15%的产率得到6'-(Bromomethyl)-1',3',3'-trimethylspiro[benzo[f][1,4]benzoxazine-3,2'-indole]
    参考文献:
    名称:
    PHOTOCHROMIC PROBES
    摘要:
    本发明提供了如权利要求1所示的光致变色化合物及其衍生物,以及这些化合物和衍生物的使用方法。本发明还提供了能够在第一状态和第二状态之间进行光导向可逆转换的光致变色光学探针。该发明还教授了确定和控制可逆光学生物分子相互作用的方法,例如在受试者中钙结合的方法。
    公开号:
    US20070195309A1
  • 作为产物:
    参考文献:
    名称:
    Family of Site-Selective Molecular Optical Switches
    摘要:
    [GRAPHIVS]We describe the design, synthesis, and characterization of a family of thiol-reactive optical switches for labeling proteins and other biomolecules. Site-selective introduction of photochromic probes within biomolecules is being used as part of a new approach for optical control of biomolecular interactions and activities within cells. The thiol-reactive photochromic probes described in this report include a spironaplithoxazine and five spirobenzopyrans. The location of the thiol-reactive group on the spirobenzopyran is different for each probe; this feature can be used to control the geometry of the optical switch within a bioconjugate. The photochromes undergo rapid and reversible, optically driven transitions between a colorless spiro (SP) state and a brightly colored merocyanine (MC) state. The MC absorption of a spironaphthoxazine conjugate is red shifted by more than 100 nm compared to the equivalent spirobenzopyran, which may be exploited for the independent control of the MC to SP transition for up to two different spironaphthoxazine and spirobenzopyran conjugates within the same sample.
    DOI:
    10.1021/jo048207o
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文献信息

  • PHOTOCHROMIC PROBES
    申请人:MARRIOTT J. D. Gerard
    公开号:US20070195309A1
    公开(公告)日:2007-08-23
    The present invention provides photochromic compounds and derivatives thereof as shown in claim 1 and methods of use of these compounds and derivatives. The present invention also provides photochromic optical probes capable of undergoing light directed reversible transition between a first state and a second state. The invention also teaches methods of determining and controlling reversible optical biomolecular interactions, for example binding of calcium in a subject.
    本发明提供了如权利要求1所示的光致变色化合物及其衍生物,以及这些化合物和衍生物的使用方法。本发明还提供了能够在第一状态和第二状态之间进行光导向可逆转换的光致变色光学探针。该发明还教授了确定和控制可逆光学生物分子相互作用的方法,例如在受试者中钙结合的方法。
  • Family of Site-Selective Molecular Optical Switches
    作者:Tomoyo Sakata、Yuling Yan、Gerard Marriott
    DOI:10.1021/jo048207o
    日期:2005.3.1
    [GRAPHIVS]We describe the design, synthesis, and characterization of a family of thiol-reactive optical switches for labeling proteins and other biomolecules. Site-selective introduction of photochromic probes within biomolecules is being used as part of a new approach for optical control of biomolecular interactions and activities within cells. The thiol-reactive photochromic probes described in this report include a spironaplithoxazine and five spirobenzopyrans. The location of the thiol-reactive group on the spirobenzopyran is different for each probe; this feature can be used to control the geometry of the optical switch within a bioconjugate. The photochromes undergo rapid and reversible, optically driven transitions between a colorless spiro (SP) state and a brightly colored merocyanine (MC) state. The MC absorption of a spironaphthoxazine conjugate is red shifted by more than 100 nm compared to the equivalent spirobenzopyran, which may be exploited for the independent control of the MC to SP transition for up to two different spironaphthoxazine and spirobenzopyran conjugates within the same sample.
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