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3-amino-2-benzoyl-6-methyl-4-(3,4,5-trimethoxyphenyl)thieno[2,3-b]pyridine-5-carboxylic acid 2-methoxyethyl ester

中文名称
——
中文别名
——
英文名称
3-amino-2-benzoyl-6-methyl-4-(3,4,5-trimethoxyphenyl)thieno[2,3-b]pyridine-5-carboxylic acid 2-methoxyethyl ester
英文别名
OSI-10267;2-Methoxyethyl 3-amino-2-benzoyl-6-methyl-4-(3,4,5-trimethoxyphenyl)thieno[2,3-b]pyridine-5-carboxylate;2-methoxyethyl 3-amino-2-benzoyl-6-methyl-4-(3,4,5-trimethoxyphenyl)thieno[2,3-b]pyridine-5-carboxylate
3-amino-2-benzoyl-6-methyl-4-(3,4,5-trimethoxyphenyl)thieno[2,3-b]pyridine-5-carboxylic acid 2-methoxyethyl ester化学式
CAS
——
化学式
C28H28N2O7S
mdl
——
分子量
536.606
InChiKey
WATFYAPVVCBCPT-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):
    5.4
  • 重原子数:
    38
  • 可旋转键数:
    11
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    147
  • 氢给体数:
    1
  • 氢受体数:
    10

反应信息

  • 作为产物:
    描述:
    E,Z-3-oxo-2-[1-(3,4,5-trimethoxyphenyl)methylidene]butyric acid 2-methoxyethyl ester 在 三乙胺 、 sodium hydroxide 作用下, 以 乙醇 为溶剂, 反应 0.58h, 生成 3-amino-2-benzoyl-6-methyl-4-(3,4,5-trimethoxyphenyl)thieno[2,3-b]pyridine-5-carboxylic acid 2-methoxyethyl ester
    参考文献:
    名称:
    Thieno[2,3-b]pyridines—A new class of multidrug resistance (MDR) modulators
    摘要:
    To identify new potent multidrug resistance modulators, we have synthesized a series of novel thieno[ 2,3-b]pyridines and furo[2,3-b] pyridines, and examined their stucture-activity relationships. All synthesized compounds were tested to determine BCRP1, P-gp, and MRP1 inhibitor activity, and most potent MDR modulators were also screened for their toxicity, cytotoxicity and Ca2+ channel antagonist activity. Among these compounds, thieno[2,3-b] pyridine (6r) was found to exhibit a potent P-gp inhibitory action with EC50 = 0.3 +/- 0.2 mu M, MRP1 inhibitory action with EC50 = 1.1 +/- 0.1 mu M and BCRP1 inhibitory action with EC50 = 0.2 +/- 0.05 mu M and may represent suitable candidate for further pharmacological studies. (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2014.09.023
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文献信息

  • THIENO [2,3-b] PYRIDINES AS MULTIDRUG RESISTANCE MODULATORS
    申请人:LATVIAN INSTITUTE OF ORGANIC SYNTHESIS
    公开号:US20160137664A1
    公开(公告)日:2016-05-19
    The thieno[2,3-b]pyridines of general formula (I), wherein R 1 is Me, C 6 H 5 , 3,4,5-(OMe) 3 C 6 H 2 , NH 2 ; R 2 is H, CN, COMe, COOC 1-4 alkyl, COOC 2 H 4 OMe, COOC 2 H 4 OPr(n); R 3 is C 6 H 4 R 6 , 3,4-OCH 2 O—C 6 H 3 ; 2-furanyl; R 6 is 4-Cl, 4-NO 2 , 4-N(C 1-4 alkyl) 2 , 3-(C 1-4 alkyloxy), 4-(C 1-4 alkyloxy), 3,4-(C 1-4 alkyloxy) 2 , 3,4,5-(C 1-4 alkyloxy) 3 ; R 4 is NH 2 , NHCOMe; R 5 is CN, COMe, COC 6 H 4 R 7 ; CO-(2-naphthyl); R 7 is H, 4-F, 4-Cl, 3-OMe, 4-OMe, 2,4-(OMe) 2 , 3,4,5-(OMe) 3 as multidrug resistance modulators to increase the effectiveness of chemotherapy in cancer treatment.
    通式为(I)的噻吩[2,3-b]吡啶,其中R1为Me,C6H5,3,4,5-(OMe)3C6H2,NH2; R2为H,CN,COMe,COOC1-4烷基,COOC2H4OMe,COOC2H4OPr(n); R3为C6H4R6,3,4-OCH2O—C6H3; 2-呋喃基; R6为4-Cl,4-NO2,4-N(C1-4烷基)2,3-(C1-4烷氧基),4-(C1-4烷氧基),3,4-(C1-4烷氧基)2,3,4,5-(C1-4烷氧基)3; R4为NH2,NHCOMe; R5为CN,COMe,COC6H4R7; CO-(2-萘基); R7为H,4-F,4-Cl,3-OMe,4-OMe,2,4-(OMe)2,3,4,5-(OMe)3,作为多药耐药调节剂,以增加癌症治疗中化疗的有效性。
  • Thieno[2,3-b]pyridines—A new class of multidrug resistance (MDR) modulators
    作者:Aivars Krauze、Signe Grinberga、Laura Krasnova、Ilze Adlere、Elina Sokolova、Ilona Domracheva、Irina Shestakova、Zigmars Andzans、Gunars Duburs
    DOI:10.1016/j.bmc.2014.09.023
    日期:2014.11
    To identify new potent multidrug resistance modulators, we have synthesized a series of novel thieno[ 2,3-b]pyridines and furo[2,3-b] pyridines, and examined their stucture-activity relationships. All synthesized compounds were tested to determine BCRP1, P-gp, and MRP1 inhibitor activity, and most potent MDR modulators were also screened for their toxicity, cytotoxicity and Ca2+ channel antagonist activity. Among these compounds, thieno[2,3-b] pyridine (6r) was found to exhibit a potent P-gp inhibitory action with EC50 = 0.3 +/- 0.2 mu M, MRP1 inhibitory action with EC50 = 1.1 +/- 0.1 mu M and BCRP1 inhibitory action with EC50 = 0.2 +/- 0.05 mu M and may represent suitable candidate for further pharmacological studies. (C) 2014 Elsevier Ltd. All rights reserved.
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