Gas chromatography–mass spectrometry of some homolycorine‐type Amaryllidaceae alkaloids

化学 石蒜科 质谱法 色谱法 石蒜科生物碱 气相色谱法 气相色谱-质谱法 串联质谱法 电喷雾电离 倍半萜 生物碱 双键 化学电离 设计药物 立体化学 有机化学 电离 离子 植物 心理学 药品 精神科 生物
作者
Strahil Berkov,Rumen Denev,Boriana Sidjimova,Yancho Zarev,Aleksandar Shkondrov,Laura Torras‐Claveria,Françesc Viladomat,Jaume Bastida
出处
期刊:Rapid Communications in Mass Spectrometry [Wiley]
卷期号:37 (12) 被引量:6
标识
DOI:10.1002/rcm.9506
摘要

Gas chromatography-mass spectrometry (GC-MS) is the most frequently applied technique for analyzing Amaryllidaceae alkaloids in plant extracts. Having these compounds, known for their potent bioactivities, is a distinctive chemotaxonomic feature of the Amaryllidoideae subfamily (Amaryllidaceae). The Amaryllidaceae alkaloids of homolycorine type with a C3-C4 double bond generally show molecular and diagnostic ions at the high-mass region with low intensity in the EIMS mode, leading to problematic identification in complex plant extracts.Eleven standard homolycorine-type alkaloids (isolated and identified by 1D and 2D nuclear magnetic resonance) were subjected to separation with GC and studied with electron impact mass spectrometry (EIMS) including single quadrupole (GC-EIMS), tandem (GC-EIMS/MS), and high-resolution (GC-HR-EIMS) detectors, as well as with chemical ionization mass spectrometry (GC-CIMS). Alkaloid fractions from two Hippeastrum species and Clivia miniata were subjected to GC-EIMS and GC-CIMS for alkaloid identification.GC-EIMS in combination with GC-CIMS provided significant structural information of homolycorine-type alkaloids with C3-C4 double bond, facilitating their unambiguous identification. Based on the obtained typical fragmentation, other 11 homolycorine-type compounds were identified in extracts from two Hippeastrum species by parallel GC-EIMS, GC-CIMS, and liquid chromatography-electrospray ionization time-of-flight mass spectrometry and in extracts from C. miniata by GC-EIMS.GC-MS can be successfully applied for the identification of new and known homolycorine-type alkaloids, among others within the Amaryllidoideae subfamily, as well as for chemotaxonomical and chemoecological studies.
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