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8-chloromethyl-3-diphenylmethoxycarbonylflavone | 579525-43-2

中文名称
——
中文别名
——
英文名称
8-chloromethyl-3-diphenylmethoxycarbonylflavone
英文别名
Benzhydryl 8-(chloromethyl)-4-oxo-2-phenylchromene-3-carboxylate
8-chloromethyl-3-diphenylmethoxycarbonylflavone化学式
CAS
579525-43-2
化学式
C30H21ClO4
mdl
——
分子量
480.947
InChiKey
MIFHLBMRVFZVKS-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):
    6.8
  • 重原子数:
    35
  • 可旋转键数:
    7
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    52.6
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

点击查看最新优质反应信息

文献信息

  • Aromatic amino acid derivates and medicinal compositions
    申请人:Endo Hitoshi
    公开号:US20050119256A1
    公开(公告)日:2005-06-02
    1. An aromatic amino acid derivative represented by the formula (I) or its pharmacologically acceptable salt: wherein, R 1 is a hydrogen atom or an amino-protecting group, R 2 is a halogen atom or an alkyl, aralkyl or aryl group, R 3 is circle over (1)} a hydrogen atom, circle over (2)} an aroylamino group, circle over (3)} a phenyl group substituted with lower alkyl, phenyl, phenoxy, etc. circle over (4)} a naphthyl or tetrahydronaphthyl group optionally substituted with hydroxy, lower alkoxy or di(lower)alkylamino, circle over (5)} an unsaturated mono-cyclic heterocyclic group containing N, O and/or S substituted with lower alkyl, phenyl, naphthyl or tetrahydroquinolyl, circle over (6)} an unsaturated or partially saturated condensed heterocyclic group containing N, O and/or S, optionally substituted with oxo, carboxy, amino, lower alkyl, etc.; X is a halogen atom, an alkyl group or an alkoxy group; Y is oxygen atom or nitrogen atom; I is 0 or 1; m is 0, 1 or 2; n is an integer of 0-5. This compound can inhibit a transporter (LAT1) of essential amino acid which is one of main nutrition for cancer cells and accordingly cause drain of the essential amino acid on the cancer cells and finally can prohibit the multiplication of cancer cells.
    一种芳香族氨基酸生物,其化学式为(I)或其药理学上可接受的盐:其中,R1为氢原子或基保护基;R2为卤素原子或烷基、芳基烷基或芳基基团;R3为circle over (1)}氢原子,circle over (2)}芳基基基团,circle over (3)}苯基,其取代基为较低的烷基、苯基、苯氧基等,circle over (4)}基或四氢基,可选地取代羟基、较低的烷氧基或二(较低)烷基基,circle over (5)}含N、O和/或S的不饱和单环杂环基团,取代基为较低的烷基、苯基、基或四氢喹啉基团,circle over (6)}含N、O和/或S的不饱和或部分饱和的紧缩杂环基团,可选地取代为氧代、羧基、基、较低的烷基等;X为卤素原子、烷基或烷氧基;Y为氧原子或氮原子;I为0或1;m为0、1或2;n为0-5的整数。该化合物可以抑制癌细胞的主要营养物质之一的必需氨基酸转运体(LAT1),从而导致癌细胞必需氨基酸的流失,最终可以抑制癌细胞的增殖。
  • Anticancer agent composition
    申请人:J-Pharma Co., Ltd.
    公开号:US10172835B2
    公开(公告)日:2019-01-08
    A method for treating cancer includes administering to a subject in need of the treatment an anticancer agent composition that includes the following agents as active ingredients; a LAT1 inhibitor, and one or more agents selected from the group consisting of an alkylating agent, a platinum-based antineoplastic agent, an anti-metabolite, a topoisomerase inhibitor, an anti-microtubule polymerizing agent, a hormonal agent, an anti-microtubule depolymerizing agent, an anticancer antibiotic, and a molecular targeted agent.
    一种治疗癌症的方法包括向需要治疗的受试者施用抗癌剂组合物,该组合物包括作为活性成分的下列制剂;LAT1抑制剂,以及选自以下组别的一种或多种制剂:烷化剂、类抗肿瘤剂、抗代谢剂、拓扑异构酶抑制剂、抗微管聚合剂、激素制剂、抗微管解聚剂、抗癌抗生素和分子靶向制剂。
  • AROMATIC AMINO ACID DERIVATIVES AND MEDICINAL COMPOSITIONS
    申请人:Endo, Hitoshi
    公开号:EP1481965B1
    公开(公告)日:2015-07-29
  • AN ANTICANCER AGENT COMPOSITION
    申请人:J-PHARMA CO., LTD.
    公开号:US20160279103A1
    公开(公告)日:2016-09-29
    A method for treating cancer includes administering to a subject in need of the treatment an anticancer agent composition that includes the following agents as active ingredients; a LAT1 inhibitor, and one or more agents selected from the group consisting of an alkylating agent, a platinum-based antineoplastic agent, an anti-metabolite, a topoisomerase inhibitor, an anti-microtubule polymerizing agent, a hormonal agent, an anti-microtubule depolymerizing agent, an anticancer antibiotic, and a molecular targeted agent.
  • US7345068B2
    申请人:——
    公开号:US7345068B2
    公开(公告)日:2008-03-18
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