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5-(5-bromothiophen-2-ylcarbonyloxymethyl)-6-[4-(furan-2-ylcarbonyloxy)-2-methoxy-phenyl]-2,2,4-trimethyl-1,2-dihydroquinoline | 1026992-19-7

分子结构分类

中文名称
——
中文别名
——
英文名称
5-(5-bromothiophen-2-ylcarbonyloxymethyl)-6-[4-(furan-2-ylcarbonyloxy)-2-methoxy-phenyl]-2,2,4-trimethyl-1,2-dihydroquinoline
英文别名
[4-[5-[(5-bromothiophene-2-carbonyl)oxymethyl]-2,2,4-trimethyl-1H-quinolin-6-yl]-3-methoxyphenyl] furan-2-carboxylate
5-(5-bromothiophen-2-ylcarbonyloxymethyl)-6-[4-(furan-2-ylcarbonyloxy)-2-methoxy-phenyl]-2,2,4-trimethyl-1,2-dihydroquinoline化学式
CAS
1026992-19-7
化学式
C30H26BrNO6S
mdl
——
分子量
608.51
InChiKey
OPYMCPHOVNKJJK-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):
    7.6
  • 重原子数:
    39
  • 可旋转键数:
    9
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    115
  • 氢给体数:
    1
  • 氢受体数:
    8

文献信息

  • NOVEL 1,2-DIHYDROQUINOLINE DERIVATIVE HAVING (SUBSTITUTED PHENYL OR SUBSTITUTED HETEROCYCLIC) CARBONYLOXY LOWER ALKYL GROUP AND ESTER-INTRODUCED PHENYL GROUP AS SUBSTITUENTS
    申请人:Matsuda Mamoru
    公开号:US20090298826A1
    公开(公告)日:2009-12-03
    The compounds represented in general formula (1) and a salt thereof are useful for glucocorticoid receptor modulator. The R 1 represents a hydrogen atom or a lower alkyl group; R 2 represents a hydrogen atom or a lower alkyl group; R 3 and R 4 may be the same or different and represent a hydrogen atom or a lower alkyl group; R 5 represents a hydrogen atom or a lower alkyl group; R 6 represents a halogen atom, a lower alkyl group, a hydroxy group, a lower alkoxy group, a nitro group or a cyano group; X represents —C(O)—, —C(O)NR 8 —, —S(O) 2 — and the like; R 7 and/or R 8 may be the same or different and represent a hydrogen atom, a lower alkyl group which may have a substituent, an aryl group which may have a substituent, a heterocyclic group which may have a substituent, a lower alkoxy group which may have a substituent and the like; Y represents a lower alkylene group; Z represents a benzene ring or a heterocyclic ring; and P represents 0, 1, 2 or 3.
    通用公式(1)中代表的化合物及其盐对糖皮质激素受体调节剂非常有用。其中,R1代表氢原子或较低的烷基基团;R2代表氢原子或较低的烷基基团;R3和R4可以相同也可以不同,代表氢原子或较低的烷基基团;R5代表氢原子或较低的烷基基团;R6代表卤素原子、较低的烷基基团、羟基、较低的烷氧基、硝基或基;X代表—C(O)—、—C(O)NR8—、—S(O)2—等;R7和/或R8可以相同也可以不同,代表氢原子、可能具有取代基团的较低烷基基团、可能具有取代基团的芳基、可能具有取代基团的杂环基团、可能具有取代基团的较低烷氧基团等;Y代表较低的烷基烯基团;Z代表苯环或杂环环;P代表0、1、2或3。
  • GLUCOCORTICOID RECEPTOR AGONIST COMPRISING 2,2,4-TRIMETHYL-6-PHENYL-1,2-DIHYDROQUINOLINE DERIVATIVES HAVING SUBSTITUTED OXY GROUP
    申请人:Kato Masatomo
    公开号:US20110118260A1
    公开(公告)日:2011-05-19
    The present invention is related to glucocorticoid receptor agonists comprised of a compound represented by formula (1) which is 2,2,4-trimethyl-6-phenyl-1,2-dihydroquinoline derivative or a salt thereof and novel pharmacological effects of the glucocorticoid receptor agonists. In the formula (1), R 1 represents formula (2a), (3a), (4a) or (5a); R 2 represents —(CO)—R8, —(CO)O—R9, or the like; R 2 —O— is substituted at the 4- or -5-position of benzene ring A; R 3 represents a lower alkyl group; R 4 , R 5 , R 6 or R 7 represents a halogen atom, a lower alkyl group which may have a substituent, or the like; m, n, p or q represents 0, 1 or the like; R 8 , R 9 or the like represents a lower alkyl group which may have a substituent, a lower alkenyl group, or the like.
    本发明涉及由式(1)表示的化合物组成的糖皮质激素受体激动剂或其盐,并且涉及糖皮质激素受体激动剂的新的药理作用。在式(1)中,R1表示式(2a)、(3a)、(4a)或(5a);R2表示—(CO)—R8、—(CO)O—R9或类似物;R2—O—在苯环A的4-或5-位上被取代;R3表示较低的烷基;R4、R5、R6或R7表示卤原子、可能具有取代基的较低的烷基或类似物;m、n、p或q表示0、1或类似物;R8、R9或类似物表示可能具有取代基的较低的烷基、较低的烯基或类似物。
  • Method for preventing or treating a disease related to the glucocorticoid receptor
    申请人:Matsuda Mamoru
    公开号:US20110263600A1
    公开(公告)日:2011-10-27
    A method for preventing or treating a disease related to the glucocorticoid receptor involving administering a pharmacologically effective amount of a 1,2-dihydroquinoline compound or a pharmaceutically acceptable salt thereof.
    一种预防或治疗与糖皮质激素受体有关的疾病的方法,包括给予一种药理学有效量的1,2-二氢喹啉化合物或其药学上可接受的盐。
  • GLUCOCORTICOID RECEPTOR AGONIST COMPOSED OF 2,2,4-TRIMETHYL-6-PHENYL-1,2-DIHYDROQUINOLINE DERIVATIVE HAVING SUBSTITUTED OXY GROUP
    申请人:AYUMI Pharmaceutical Corporation
    公开号:EP2319835B1
    公开(公告)日:2016-04-13
  • 1,2-DIHYDROQUINOLINE DERIVATIVE HAVING (SUBSTITUTED PHENYL OR SUBSTITUTED HETEROCYCLIC) CARBONYLOXY LOWER ALKYL GROUP AND ESTER-INTRODUCED PHENYL GROUP AS SUBSTITUENTS
    申请人:Santen Pharmaceutical Co., Ltd
    公开号:EP2085389B1
    公开(公告)日:2012-09-26
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同类化合物

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