Synthesis and Cytotoxicity of Cantharidinimide Dimers and Imide Analogues
碩士 === 臺北醫學大學 === 藥學系 === 93 === Mylabris phalerata, Meloidae family of Coleoptera, has been known since antiquity to produce a potent toxic defensive agent, known as cantharidin (exo,exo-2,3-dimethyl-7-oxabicyclo [2.2.1] heptane-2,3- dicarboxylic anhydride), but well-known as Spanish Fly. In the pa...
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ndltd-TW-093TMC005510222015-12-25T04:10:27Z http://ndltd.ncl.edu.tw/handle/44565212090029989950 Synthesis and Cytotoxicity of Cantharidinimide Dimers and Imide Analogues 斑蝥胺素衍生物的合成與細胞毒性之探討 Yu-Huan Lee 李毓寰 碩士 臺北醫學大學 藥學系 93 Mylabris phalerata, Meloidae family of Coleoptera, has been known since antiquity to produce a potent toxic defensive agent, known as cantharidin (exo,exo-2,3-dimethyl-7-oxabicyclo [2.2.1] heptane-2,3- dicarboxylic anhydride), but well-known as Spanish Fly. In the past, Cantharidin has used as anticancer, herbicidal, pesticide and treatment of hepatic carcinoma and molluscum contagiosum activities.We used cantharidin and serious of diaminoalkane as starting materials, by heating 200℃ in sealed tube to form various cantharidinimide dimer. The other hand, we utilized various N-activated aziridine derivatives as starting materials, reacted with cantharidinimide and different imide analogous to obtain serial derivatives. All of the products were measured by 1H-NMR, IR, High-resolution mass spectrometry. In addition, we evaluated these compounds in cytotoxicity. Pen-Yuan Lin 林本元 2005 學位論文 ; thesis 94 zh-TW |
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碩士 === 臺北醫學大學 === 藥學系 === 93 === Mylabris phalerata, Meloidae family of Coleoptera, has been known since antiquity to produce a potent toxic defensive agent, known as cantharidin (exo,exo-2,3-dimethyl-7-oxabicyclo [2.2.1] heptane-2,3- dicarboxylic anhydride), but well-known as Spanish Fly. In the past, Cantharidin has used as anticancer, herbicidal, pesticide and treatment of hepatic carcinoma and molluscum contagiosum activities.We used cantharidin and serious of diaminoalkane as starting materials, by heating 200℃ in sealed tube to form various cantharidinimide dimer. The other hand, we utilized various N-activated aziridine derivatives as starting materials, reacted with cantharidinimide and different imide analogous to obtain serial derivatives. All of the products were measured by 1H-NMR, IR, High-resolution mass spectrometry. In addition, we evaluated these compounds in cytotoxicity.
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author2 |
Pen-Yuan Lin |
author_facet |
Pen-Yuan Lin Yu-Huan Lee 李毓寰 |
author |
Yu-Huan Lee 李毓寰 |
spellingShingle |
Yu-Huan Lee 李毓寰 Synthesis and Cytotoxicity of Cantharidinimide Dimers and Imide Analogues |
author_sort |
Yu-Huan Lee |
title |
Synthesis and Cytotoxicity of Cantharidinimide Dimers and Imide Analogues |
title_short |
Synthesis and Cytotoxicity of Cantharidinimide Dimers and Imide Analogues |
title_full |
Synthesis and Cytotoxicity of Cantharidinimide Dimers and Imide Analogues |
title_fullStr |
Synthesis and Cytotoxicity of Cantharidinimide Dimers and Imide Analogues |
title_full_unstemmed |
Synthesis and Cytotoxicity of Cantharidinimide Dimers and Imide Analogues |
title_sort |
synthesis and cytotoxicity of cantharidinimide dimers and imide analogues |
publishDate |
2005 |
url |
http://ndltd.ncl.edu.tw/handle/44565212090029989950 |
work_keys_str_mv |
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