Coumarin Acetylenes & Propargyl Ethers, a New Class of Cytochrome P450 Inhibitors

香豆素乙炔

• 批准号: 6727029
• 负责人: MARYAM FOROOZESH
• 金额: $ 9.49万
• 依托单位: XAVIER UNIVERSITY OF LOUISIANA
• 依托单位国家: 美国
• 财政年份: 2004
• 资助国家: 美国
• 起止时间: 2004-04-01 至 2008-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6727029
• 关键词: active sites; alkynes; alpha benzopyrone; carcinogenesis; chemical structure function; chemical synthesis; cytochrome P450; enzyme inhibitors; enzyme substrate analog; ethers; isozymes; laboratory rat

Cytochrome P450 enzymes are a superfamily of hemoproteins involved in the metabolism of endogenous and xenobiotic compounds. The goal of this project is to synthesize and study a number of new potentially selective mechanism-based inactivators for certain P450 enzymes involved in carcinogenesis. In our previous studies, we have established that a number of aromatic acetylenes and certain propargyl ethers are selective suicide inhibitors of cytochrome P450-dependent monooxygenases. In this project, we propose to synthesize a new class of compounds containing a coumarin ring structure, with a propargyl ether or ethynyl moiety. We are planning to synthesize propargyl substituted coumarins, as well as ethynyl substituted coumarins, and assay them in-vitro on a number of P450 enzymes in order to study their relative potential inhibitory effects based on the type, placement, and number of the substituents on the ring system. Due to their structural similarities to coumarin, 7-ethoxycoumarin, and 7-ethoxy-4-trifluoromethylcoumarin (known coumarin P450 substrates), these compounds should interact with human P450 enzymes 2A6, 1A2, 2B1, and 2E1, as well as rat P450s 1A1, 1A2, and 2B1. However the presence or absence of an oxygen on the substituent containing the triple bond should change the polarity, and the shape of the branch, leading to some differences in the interaction with various P450 enzymes' active sites, and hopefully causing selective mechanism-based (suicide) inhibition. The above-mentioned P450 enzymes are extremely important in the metabolism of pharmaceuticals and environmental chemicals including procarcinogens. Due to the special properties of suicide inhibitors, these compounds are useful tools in the studies of cancer development and treatment. Additionally, The mechanism of action of these inhibitors makes it possible to use them as probes into the active sites of P450 enzymes, facilitating the identification of important amino acid residues, leading to better understanding of the structure-activity relationships involved in the P450-dependent reactions.

细胞色素P450酶是血色素蛋白的超家族，参与细胞色素P450的代谢。 内源化合物和异源化合物。这个项目的目标是合成和研究一些新的潜在的选择性机制为基础的某些P450酶与致癌相关的灭活剂。在我们以前的研究中，我们已经确定一些芳香烃和某些炔丙基醚是细胞色素P450依赖的单加氧酶的选择性自杀抑制物。在这个项目中，我们建议合成一类新的含有香豆素环结构的化合物，带有炔丙基醚或乙炔基。我们计划合成炔丙基取代香豆素和乙炔基取代香豆素，并在体外对一些P450酶进行检测，以研究它们在环上取代基的类型、位置和数量的相对潜在抑制作用。由于它们与香豆素、7-乙氧基香豆素和7-乙氧基-4-三氟甲基香豆素(已知的香豆素P450底物)的结构相似，这些化合物应该与人P450酶2A6、1A2、2B1和2E1以及大鼠相互作用 P450 1A1、1A2和2B1。然而，含有三键的取代基上氧的存在或不存在应该改变支链的极性和形状，导致与各种P450酶活性部位的相互作用的一些差异，并有望引起基于选择性机制的(自杀)抑制。上述P450酶在药物和包括致癌物原在内的环境化学品的新陈代谢中非常重要。由于自杀抑制剂的特殊性质，这些化合物是 癌症发展和治疗研究中的有用工具。此外，这些抑制剂的作用机制使其有可能被用作P450酶活性部位的探针，有助于识别重要的氨基酸残基，从而更好地理解P450依赖反应中涉及的结构-活性关系。