| 摘要: | 中 文 摘 要 抗不整脈藥物氧基小蘗鹼類似物之合成研究 8-氧基小蘗
鹼(JKL 1073A)(2)是一個小蘗鹼(1)的衍生物，初步藥理實驗中發現其具
有加強心臟收縮力及減緩心跳具有抗不整脈的作用，並對於缺氧及
ouabain所引起的心律不整有改善的作用；為了進一步了解其化學結構與
抗心律不整作用之間的相關性，我們使用化學合成方法製備了數種氧基小
蘗鹼衍生物，以供藥理實驗測定之用。化學合成方法是以四級化原小蘗鹼
型衍生物之鹽類作為關鍵性中間化合物，加入30% NaOH水溶液進行類似
Cannizzaro機轉的反應，得到七種8-氧基原小蘗鹼衍生物分別為化合物2,
14, 17, 58, 59, 60, 61, 63及64。取化合物2及58，於鹽酸水溶液中加
熱進行O-demethylation反應，得到化合物63及64。第十三位氧化的原小
蘗鹼衍生物也同時被製備，主要是利用小蘗鹼氯鹽(1)作為起始原料，先
經NaBH4還原作用形成dihydroberberine(15)，再以m-chloroperbenzoic
acid氧化，即可得到第十三位氧化的berberinephenolbetaine(26)，以此
作為一重要的中間產物，當使用1-propanol為溶媒並以NaBH4還原時，可
以得到ophiocarpine(20)及epiophiocarpine(21)兩種產物；若
berberinephenolbetaine(26)分別與鹽酸甲醇溶液或甲基碘試劑反應，則
得到13-hydroxyberberinium Chloride(65)或13-methoxyberberinium
iodide(66)二種產物。以化學合成的十三種化合物均經紅外光譜、氫光譜
、碳光譜及質譜等光譜分析鑑定結構。部份包含中間產物的二十個化合物
是以大白鼠之離體心臟作有關心收縮力與心跳速率之藥理活性測試。結果
顯示化合物15及66可增加心收縮力和減緩自發性的右心房心跳速率，作用
較JKL 1073A(2)為佳；而化合物54則是在加強右心室心收縮力方面比JKL
1073A(2)更強。後續部份化合物有關其抗心律不整的藥理活性，目前正在
評估測試中。
AbstractSynthesis of 8-Oxoberberine Analogues as Potential
Antiarrhythmic Agents 8-Oxoberberine (JKL 1073A) (2) is a analog
of berberine(1), exhibited a positive inotropic effect and
negative chronotropic effect. Besides the positive inotropic
effect, it also possessed antiarrhythmic activity against
cardiac arrhythmia induced by ouabain and hypoxia. Therefore,
several analogues modeled after 8-oxoberberine (2) were prepared
by chemical synthesis in order to evaluate the relationship
between their structures and antiarrhythmic activity.
Protoberberinium salts were used as key intermediates. Treatment
of protoberberinium salts with 30% NaOH in aqueous solution, by
the Cannizzaro mechanism, to yield seven 8-oxoprotoberberine
derivatives 2, 14, 17, 58, 59, 60 and 61. O-Demethylation of
compounds 2 and 58 with hydrochloric acid afforded the phenolic
compounds 63 and 64.13-Oxygenated protoberberines were also
perpared berberine chloride were reduced by NaBH4 to give
dihydroberberine (15). Oxidation of dihydroberberine (15) by m-
chloroperbenzoic acid gave berberine phenolbetaine (26) and
following by NaBH4 reduction in 1-propanol to yield
ophiocarpine(20) and epiophiocarpine(21). Reaction of
berberinephenolbetaine(26) with hydrochloride or methyl iodide,
gave the 13-hydroxyberberinium chloride(65) or
13-methoxyberberinium iodide(66). The structures of these
synthetic analogues are consistent with the spectral data of IR,
PMR, CMR and Mass spectra.Twenty compounds including
intermediates were evaluated with the isolated heart preparation
from rats to determine the chronotropic and inotropic effects.
The result indicated that compounds 15 and 66 have stronger
effects in postive inotropic and negative chronotropic
activities than that of JKL 1073A 2. Compound 54 showed more
potent in positive inotropic effect than that of JKL 1073A 2 in
right ventricle preparation.The evaluation of some other
synthetic analogues on the isolated heart preparation is under
investigated. |
