5-methylseselin | 104556-36-7

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 香豆素及其衍生物
• 英文名称: 5-methylseselin
• 英文别名: 5,8,8-Trimethylpyrano[2,3-f]chromen-2-one
• CAS: 104556-36-7
• 化学式: C₁₅H₁₄O₃
• 分子量: 242.274
• InChiKey: ABBLQUAEMDCGKZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  18
• 可旋转键数：
  0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  35.5
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  5-methylseselin 在 吡啶 、 potassium osmate(VI) 、 甲基磺酰胺 、 水 、 potassium carbonate 、 (DHQD)2吡啶 、 potassium hexacyanoferrate(III) 作用下， 以 二氯甲烷 、 叔丁醇 为溶剂， 反应 24.0h， 生成 3′S,4′S-di-O-(4-chlorobenzoyl)-5-methyl-(-)-cis-khellactone
  参考文献：
  名称：

  Synthesis and cytotoxic activities of novel 4-methoxy-substituted and 5-methyl-substituted (3&prime;<em>S</em>,4&prime;<em>S</em>)-(-)-<em>cis</em>-khellactone derivatives that induce apoptosis via the intrinsic pathway

  摘要：

  This study deals with the design and synthesis of a series of novel 4-methoxy-substituted and 5-methyl-substituted (3'S, 4'S)-(-)-cis-khellactones. The newly synthesized compounds were characterized by H-1 nuclear magnetic resonance (NMR), C-13-NMR, mass spectrometry, and elemental analysis. All the derivatives were subjected to in vitro cytotoxicity screening against HEPG-2 (human liver carcinoma), SGC-7901 (human gastric carcinoma), and LS174T (human colon carcinoma), by using the MTT assay. The results revealed that several of the 4-methoxy-substituted compounds exhibited potent cytotoxicity. Among these, compound 12e showed the highest activity against cancer cells which 50% inhibitory concentration (IC50) values were in the range of 6.1-9.2 mu M with low toxicity on normal human hepatocyte. Preliminary investigation of possible mechanisms of action of compound 12e against HEPG-2 cells indicated possible induction of apoptosis, as determined by morphological observations and Annexin V/propidium iodide (PI) double staining, in addition to apparent dissipation of mitochondrial membrane potential (MMP), as measured by 5,5', 6,6'-tetrachloro-1,1', 3,3'-tetraethyl-imidacarbocyanine iodide (JC-1) staining in combination with the activation of caspase-9 and caspase-3 by Western blot analysis. Overall, the data suggest that compound 12e may be a promising potential anticancer agent that could act primarily by inducing apoptosis through the mitochondria-mediated intrinsic pathway in human hepatoma cells.

  DOI：

  10.2147/dddt.s131753
• 作为产物：
  描述：

  6-formyl-5-hydroxy-2,2,7-trimethyl-3,4-dihydro-2H-1-benzopyran 在 sodium acetate 、 2,3-二氯-5,6-二氰基-1,4-苯醌 作用下， 以 苯 为溶剂， 反应 84.0h， 生成 5-methylseselin
  参考文献：
  名称：

  Ahluwalia, V. K.; Gupta, Ranjna, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1986, vol. 25, p. 51 - 55

  摘要：

  DOI：

文献信息

• Anti-AIDS Agents. 37. Synthesis and Structure−Activity Relationships of (3‘<i>R</i>,4‘<i>R</i>)-(+)-<i>cis</i>-Khellactone Derivatives as Novel Potent Anti-HIV Agents
  作者：Lan Xie、Yasuo Takeuchi、L. Mark Cosentino、Kuo-Hsiung Lee

  DOI：10.1021/jm9900624

  日期：1999.7.1

  (+)-cis-khellactone derivatives as novel anti-HIV agents, 24 monosubstituted 3', 4'-di-O-(S)-camphanoyl-(+)-cis-khellactone (DCK) derivatives were synthesized asymmetrically. These compounds included 4 isomeric monomethoxy analogues (3-6), 4 isomeric monomethyl analogues (7-10), 4 4-alkyl/aryl-substituted analogues (11-14), and 12 4-methyl-(+)-cis-khellactone derivatives (15-26) with varying 3', 4'-substituents

  为了探索作为新型抗HIV药物的（+）-顺式-khellactone衍生物的结构要求，使用24个单取代的3'，4'-di-O-（S）-樟脑酰基-（+）-顺式-khellactone（DCK）衍生物不对称合成。这些化合物包括4个异构的单甲氧基类似物（3-6），4个异构的单甲基类似物（7-10），4个4-烷基/芳基取代的类似物（11-14）和12个4-甲基-（+）-顺式具有3'，4'取代基的khellactone衍生物（15-26）。这些（+）-顺式-khellactone衍生物被筛选针对急性感染的H9淋巴细胞中的HIV-1复制。结果表明，（3'R，4'R）-（+）-顺式-khellactone骨架，3'-和4'-位置的两个（S）-（-）-樟脑酰基和甲基除6-位以外，香豆素环上的α是抗HIV活性的最佳结构部分。3-甲基-（7），4-甲基-（8）和5-甲基-（9）3'，4'-二-O-（S）-樟脑酰基-（3'R，4'R）-
• Anti-aids agents 33.1 Synthesis and anti-HIV activity of mono-methyl substituted 3′,4′-di-O-(−)-camphanoyl-(+)-cis-khellactone (DCK) analogues
  作者：Lan Xie、Yasuo Takeuchi、L. Mark Cosentino、Kuo-Hsiung Lee

  DOI：10.1016/s0960-894x(98)00367-9

  日期：1998.8

  substituted DCK analogues (2-5) were asymmetrically synthesized from different starting materials. 3-Methyl, 4-methyl, and 5-methyl-3',4'-di-O-(-)-camphanoyl-(+)-cis-khellactone (2-4) all were extremely potent against HIV-1 replication in H9 lymphocyte cells with EC50 and therapeutic index values of < 4.23 x 10(-7) microM and > 3.72 x 10(8), respectively, which are much better than those of DCK and AZT

  从不同的起始原料不对称合成了四个异构的甲基取代的DCK类似物（2-5）。3-甲基，4-甲基和5-甲基-3'，4'-二-O-（-）-樟脑酰基-（+）-顺式-甲壳酮（2-4）对HIV-1复制都非常有效H9淋巴细胞中的EC50值分别为<4.23 x 10（-7）microM和> 3.72 x 10（8），这比本实验中DCK和AZT的要好得多。
• Selenium-Based Solid-Phase Synthesis of Benzopyrans I: Applications to Combinatorial Synthesis of Natural Products
  作者：K. C. Nicolaou、Jeffrey A. Pfefferkorn、Guo-Qiang Cao

  DOI：10.1002/(sici)1521-3773(20000218)39:4<734::aid-anie734>3.0.co;2-i

  日期：2000.2.18
• AHLUWALIA V. K.; GUPTA RANJNA, INDIAN J. CHEM., 25,(1986) N 1, 51-55
  作者：AHLUWALIA V. K.、 GUPTA RANJNA

  DOI：——

  日期：——
• Ahluwalia, V. K.; Gupta, Ranjna, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1986, vol. 25, p. 51 - 55
  作者：Ahluwalia, V. K.、Gupta, Ranjna

  DOI：——

  日期：——