4-(2-((3-carboxypropanoyl)oxy)ethoxy)-3-(phenylsulfonyl)-1,2,5-oxadiazole-2-oxide | 1186196-63-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 4-(2-((3-carboxypropanoyl)oxy)ethoxy)-3-(phenylsulfonyl)-1,2,5-oxadiazole-2-oxide
• 英文别名: 4-[2-[[4-(Benzenesulfonyl)-5-oxido-1,2,5-oxadiazol-5-ium-3-yl]oxy]ethoxy]-4-oxobutanoic acid；4-[2-[[4-(benzenesulfonyl)-5-oxido-1,2,5-oxadiazol-5-ium-3-yl]oxy]ethoxy]-4-oxobutanoic acid
• CAS: 1186196-63-3
• 化学式: C₁₄H₁₄N₂O₉S
• 分子量: 386.339
• InChiKey: LWLUVLWZEXWQQX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.7
• 重原子数：
  26
• 可旋转键数：
  10
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  167
• 氢给体数：
  1
• 氢受体数：
  10

反应信息

• 作为反应物：
  描述：

  4-(2-((3-carboxypropanoyl)oxy)ethoxy)-3-(phenylsulfonyl)-1,2,5-oxadiazole-2-oxide 、 1,2,3,4-四氢罂粟碱 在 4-二甲氨基吡啶 、 N,N'-二环己基碳二亚胺 作用下， 以 二氯甲烷 为溶剂， 反应 4.0h， 以47%的产率得到2-[[4-(benzenesulfonyl)-5-oxido-1,2,5-oxadiazol-5-ium-3-yl]oxy]ethyl 4-[1-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl]-4-oxobutanoate
  参考文献：
  名称：

  Synthesis and evaluation of furoxan-based nitric oxide-releasing derivatives of tetrahydroisoquinoline as anticancer and multidrug resistance reversal agents

  摘要：

  Multidrug resistance in tumor cells poses a major obstacle to efficient chemotherapy. Several types of agents have been recognized as multidrug resistance inhibitors, among which the tetrahydroisoquinolines is the most studied. In current study 16 furoxan-based nitric oxide-releasing derivatives of tetrahydroisoquinoline were synthesized. Their cytotoxic activities and effects in reversing multidrug resistance have been evaluated. The results revealed that these compounds had moderate cytotoxic effects. Compounds 7a-f, 7h, and 7l showed higher cytotoxicities than the rest, but lower than adriamycin on K562 cell line. Compounds 7d, 7f, and 7l exhibited potent MDR reversal activities on K562/A02 cell line. The accumulation assay indicated that compounds 7d, 7f, and 7l significantly increased the intracellular accumulation of rhodamine123 in K562/A02 cells. Furthermore, these three compounds produced high concentrations of NO in K562/A02 cells. Potentially, the high concentrations of NO produced by NO donor moieties will lead to an increased cytotoxicity to K562/A02 cells. Our results suggested that compounds 7d, 7f, and 7l had anticancer effects, as well as multidrug resistance reversal effects. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2011.07.077
• 作为产物：
  描述：

  苯硫基乙酸 在 4-二甲氨基吡啶 、 双氧水 、 溶剂黄146 、 三乙胺 、 sodium hydroxide 作用下， 以 四氢呋喃 、 二氯甲烷 、 水 为溶剂， 反应 7.0h， 生成 4-(2-((3-carboxypropanoyl)oxy)ethoxy)-3-(phenylsulfonyl)-1,2,5-oxadiazole-2-oxide
  参考文献：
  名称：

  布雷菲德菌素A的4,7-位双呋咱NO供体取代 衍生物及其制备方法和用途

  摘要：

  本发明涉及药物化学领域，涉及布雷菲德菌素A的4,7‑位同时进行修饰的衍生物。具体涉及4,7‑位呋咱类NO供体取代的布雷菲德菌素A衍生物及其制备方法和在制备抗肿瘤药物中的用途。所述的布雷菲德菌素A衍生物如通式I或II所示，其中，m、n分别为1‑8的整数。

  公开号：

  CN106928213B

文献信息

• Synthesis and Biological Evaluation of Novel Furozan-Based Nitric Oxide-Releasing Derivatives of Oridonin as Potential Anti-Tumor Agents
  作者：Dahong Li、Lei Wang、Hao Cai、Yihua Zhang、Jinyi Xu

  DOI：10.3390/molecules17067556

  日期：——

  To search for novel nitric oxide (NO) releasing anti-tumor agents, a series of novel furoxan/oridonin hybrids were designed and synthesized. Firstly, the nitrate/nitrite levels in the cell lysates were tested by a Griess assay and the results showed that these furoxan-based NO-releasing derivatives could produce high levels of NO in vitro. Then the anti-proliferative activity of these hybrids against four human cancer cell lines was also determined, among which, 9h exhibited the most potential anti-tumor activity with IC50 values of 1.82 µM against K562, 1.81 µM against MGC-803 and 0.86 µM against Bel-7402, respectively. Preliminary structure-activity relationship was concluded based on the experimental data obtained. These results suggested that NO-donor/natural product hybrids may provide a promising approach for the discovery of novel anti-tumor agents.

  为寻找新型一氧化氮（NO）释放抗肿瘤剂，设计并合成了一系列新型呋咱/冬凌草甲素杂化物。首先，通过Griess试剂盒检测细胞裂解液中的硝酸盐/亚硝酸盐水平，结果显示这些基于呋咱的NO释放衍生物在体外能产生高水平的NO。随后测定了这些杂化物对四种人类癌细胞系的抗增殖活性，其中9h表现出了最大的抗癌潜力，对K562、MGC-803和Bel-7402的IC50值分别为1.82 µM、1.81 µM和0.86 µM。根据所得实验数据，得出了初步的构效关系结论。这些结果表明，NO供体/天然产物杂化物可能是发现新型抗肿瘤药物的有前景途径。
• 一类具有抗肿瘤活性的呋咱类NO供体型吴茱 萸碱衍生物
  申请人：沈阳药科大学

  公开号：CN105622607B

  公开（公告）日：2017-04-26

  本发明涉及天然药物及药物化学领域，具体涉及吴茱萸碱13‑N位进行修饰的衍生物。本发明公开了这些13‑N位呋咱类NO供体取代的吴茱萸碱衍生物的制备方法及抗肿瘤活性评价。所述的化合物结构如下：其中，R1、R2为(CH2)n 或 (CH2) n1O(CH2) n2,n、n1、n2为1‑8的整数。。
• Discovery of novel antitumor nitric oxide-donating β -elemene hybrids through inhibiting the PI3K/Akt pathway
  作者：Jichao Chen、Tianyu Wang、Shengtao Xu、Pengfei Zhang、Aijun Lin、Liang Wu、Hequan Yao、Weijia Xie、Zheying Zhu、Jinyi Xu

  DOI：10.1016/j.ejmech.2017.04.045

  日期：2017.7

  sensitivity to U87 cells with IC50 values ranging from 173 to 2 nM. Moreover, most compounds produced high levels of NO in vitro, and the antitumor activity of 11a in U87 cells was markedly attenuated by an NO scavenger (hemoglobin or carboxy-PTIO). Further mechanism studies revealed that 11a caused the G2 phase arrest of the cell cycle and induced apoptosis of U87 cells by preventing the activation of the

  设计并合成了一系列新颖的基于呋喃烷的NO供体β-榄香烯杂种，以提高天然β-榄香烯的抗癌功效。生物测定结果表明，与母体化合物β-榄香烯相比，所有目标化合物对三种癌细胞系（SGC-7901，HeLa和U87）均表现出显着改善的抗增殖活性。有趣的是，这些化合物对U87细胞显示出极好的敏感性，IC50值为173至2 nM。而且，大多数化合物在体外产生高水平的NO，并且NO清除剂（血红蛋白或羧基-PTIO）显着减弱U87细胞中11a的抗肿瘤活性。进一步的机理研究表明，11a通过阻止PI3K / Akt通路的激活，导致细胞周期的G2期停滞并诱导U87细胞凋亡。而且，11a显着抑制了H22肝癌异种移植小鼠模型中的肿瘤生长，其肿瘤抑制率（TIR）为64.8％，优于相同剂量60 mg / kg的β-榄香烯（TIR，49.6％）。在一起，这些新颖的NO供体β-榄香烯衍生物的显着生物学特征可能使它们成为有希望的人癌症干预候选者。
• 吩噻嗪类化合物及其应用
  申请人：天津国际生物医药联合研究院

  公开号：CN109761932A

  公开（公告）日：2019-05-17

  本发明提供了吩噻嗪类化合物及其在制备乳腺癌和黑色素瘤的药物中的应用。吩噻嗪类化合物对乳腺癌细胞MDA‑MB‑231、SUM159、MCF‑7、SKBR‑3和黑色素瘤细胞A375、B16BL6的抑制活性高于三氟拉嗪和硫利达嗪，可以应用于治疗乳腺癌和黑色素瘤。其中，吩噻嗪类化合物的通式为：其中，R1为R2为其中，n＝1、2、3或4；X为O或N。
• Synthesis and Bioactivity of Furoxan-Based Nitric Oxide-Releasing Colchicine Derivatives as Anticancer Agents
  作者：Li Hong Shen、Sheng Li Wang、Hong Yu Li、Yi Sheng Lai、Li Jie Liu

  DOI：10.14233/ajchem.2013.13635

  日期：——

  A series of novel nitric oxide-donating colchicine derivatives (9a-j) were synthesized by coupling furoxan with N-methyl colchiceinamide through an appropriate spacer arm and their cytotoxicity against four human cancer cell lines in vitro were evaluated by MTT method. It was found that many of the derivatives displayed significant activity, particularly, compound 9f showed more potent cytotoxic activities than colchicine.

  通过将呋喃并[1,2-a]唑酮与N-甲基秋水仙酰胺通过适当的间隔臂偶联，合成了一系列新的NO供体型秋水仙碱衍生物（9a-j），并采用MTT法评估了它们对四种人癌细胞系的体外细胞毒性。结果发现，许多衍生物表现出显著的活性，特别是化合物9f的细胞毒性活性显著强于秋水仙碱。