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机构地区:[1]中山大学测试中心,广州510275 [2]南京林业大学化学工程学院,南京210037
出 处:《高等学校化学学报》2011年第4期863-867,共5页Chemical Journal of Chinese Universities
基 金:国家自然科学基金(批准号:30771688;30871989)资助
摘 要:采用电喷雾质谱法研究了4种新合成的N-苯甲酰基-脱氢枞胺衍生物(NBDD)———N-苯甲酰基-脱氢枞胺(NBD)、N-邻氯苯甲酰基-脱氢枞胺(NClBD)、N-苯甲酰基-脱氢枞胺-7-酮(NBDO)和N-邻氯苯甲酰基-脱氢枞胺-7-酮(NClBDO)与血管紧张肽Ⅲ(AngⅢ)的相互作用.结果表明,这4种化合物分别与AngⅢ以摩尔比1∶1,3∶1和5∶1混合时,均可形成化学结合计量比为1∶1和2∶1的非共价复合物,这些复合物主要电离为+2价离子[NBDD-AngⅢ+2H]2+和[(NBDD)2-AngⅢ+2H]2+.化学结合计量比为1∶1的NBDD-AngⅢ复合物+2价离子的稳定性顺序为:NBDO-AngⅢ>NClBDO-AngⅢ>NClBD-AngⅢ>NBD-AngⅢ;在化学结合计量比为2∶1的(NBDD)2-AngⅢ复合物中,2个NBDD分子与AngⅢ的结合形式为NBDD-AngⅢ-NBDD.The interactions between the novel N-benzoyl-dehydroabietylamine derivatives(NBDD)including N-benzoyl-dehydroabietylamine(NBD),N-o-chlorobenzoyl-dehydroabietylamine(NClBD),N-benzoyl-dehydroabietylamine-7-one(NBDO) and N-o-chlorobenzoyl-dehydroabietylamine-7-one(NClBDO) with angiotensin Ⅲ(AngⅢ) were investigated by electrospray ionization mass spectrometry(ESI-MS).The results show that when the four derivatives respectively mixed with Ang Ⅲ in molar ratios of NBDD∶AngⅢ 1∶1,3∶1 and 5∶1,the non-covalent complexes with binding stoichiometries of 1∶1 NBDD-AngⅢ and 2∶1(NBDD)2-AngⅢ formed and the complexes mainly formed+2 charged ions [NBDD-AngⅢ+2H]2+ and [(NBDD)2-AngⅢ+2H]2+.The stability order of the four kinds of complex ions of binding stoichiometries of 1∶1 [NBDD-AngⅢ+2H]2+ was NBDO-AngⅢNClBDO-AngⅢNClBD-AngⅢNBD-AngⅢ.And for the complexes of binding stoichiometries of 2∶1(NBDD)2-AngⅢ,the combination mode of two NBDD molecules with AngⅢ was NBDD-AngⅢ-NBDD.
关 键 词:电喷雾质谱 N-苯甲酰基-脱氢枞胺衍生物 血管紧张肽Ⅲ 相互作用
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