Colchicinoids from Colchicum crocifolium Boiss.:: a case study in dereplication strategies for (-)-colchicine and related analogues using LC-MS and LC-PDA techniques

被引:20
作者
Alali, Feras Q. [1 ]
Gharaibeh, Ahmad [2 ]
Ghawanmeh, Abdullah [2 ]
Tawaha, Khaled [3 ]
Oberlies, Nicholas H. [4 ]
机构
[1] Jordan Univ Sci & Technol, Fac Pharm, Dept Med Chem & Pharmacognosy, Irbid 22110, Jordan
[2] Jordan Univ Sci & Technol, Fac Sci & Arts, Dept Appl Chem, Irbid 22110, Jordan
[3] Univ Jordan, Dept Pharmaceut Sci, Fac Pharm, Amman 11942, Jordan
[4] Res Triangle Inst, Nat Prod Lab, Res Triangle Pk, NC 27709 USA
关键词
bioactive natural products; hyphenated techniques; Jordanian medicinal plants; biodiversity; Colchicaceae;
D O I
10.1002/pca.1060
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
As a part of a project designed to investigate Colchicum species in Jordan, the chemical constituents of Colchicum crocifolium Boiss. (Colchicaceae) were investigated using LC-MS and LC-UV/Vis PDA. A decision tree for working with colchicinods has been developed by incorporating data from LC-UV/PDA and LC-MS. This dereplication strategy draws upon the UV/PDA spectra to classify compounds into one of four structural groups and combines this with retention time and mass spectra/molecular weight to identify the compounds. This strategy was applied on a small amount of extract (2 mg) of Colchicum crocifolium to dereplicate 10 known compounds from four different structural groups, namely (-)-demecolcine, 2-demethyl-(-)-colchicine or 3-demethyl-(-)-colchicine, N-deacetyl-(-)-colchicine, (-)-colchicine, (-)-colchicine, beta-lumidemecolcine, 2-demethyl-beta-lumicolchicine or 3-demethyl-beta-lumicolchicine, N,N-dimethyl-N-deacetyl-beta-lumicornigerine, (-)-isoandrocymbine and (-)-autumnaline. Furthermore, a new compound was identified as N,N-dimethyl-N-deacetyl-(-)-cornigerine. Three compounds, which had molecular ions at m/z 325, 340 and 374, could not be dereplicated into any obvious structural classes that have been isolated in our laboratories previously or reported in the literature. Copyright (c) 2008 John Wiley & Sons, Ltd.
引用
收藏
页码:385 / 394
页数:10
相关论文
共 34 条
[1]  
Al-Eisawi DM, 1998, FIELD GUIDE WILD FLO
[2]   Phytochemical study and cytotoxicity evaluation of Colchicum stevenii Kunth (Colchicaceae):: A Jordanian meadow saffron [J].
Al-Mahmoud, MS ;
Alali, FQ ;
Tawaha, K ;
Qasaymeh, RM .
NATURAL PRODUCT RESEARCH, 2006, 20 (02) :153-160
[3]  
ALALI F, 2005, ACTA PHARM TURC, V47, P143
[4]  
Alali FQ, 2006, NAT PROD COMMUN, V1, P95
[5]   Phytochemical studies and cytotoxicity evaluations of Colchicum tunicatum Feinbr and Colchicum hierosolymitanum Feinbr (Colchicaceae):: two native Jordanian meadow saffrons [J].
Alali, Feras Q. ;
Tawaha, Khaled ;
El-Elimat, Tamam ;
Qasaymeh, Rana ;
Li, Chen ;
Burgess, Jason ;
Nakanishi, Yuka ;
Kroll, David J. ;
Wani, Mansukh C. ;
Oberlies, Nicholas H. .
NATURAL PRODUCT RESEARCH, 2006, 20 (06) :558-566
[6]   Seasonal variation of colchicine content in Colchicum hrachyphyllum and Colchicum tunicatum (Colchicaceae) [J].
Alali, Feras Q. ;
El-Alali, Abdullah ;
Tawaha, Khaled ;
El-Elimat, Tamam .
NATURAL PRODUCT RESEARCH, 2006, 20 (12) :1121-1128
[7]   New colchicinoids from a native Jordanian meadow saffron, Colchicum brachyphyllum:: Isolation of the first naturally occurring dextrorotatory colchicinoid [J].
Alali, FQ ;
El-Elimat, T ;
Li, C ;
Qandil, A ;
Alkofahi, A ;
Tawaha, K ;
Burgess, JP ;
Nakanishi, Y ;
Kroll, DJ ;
Navarro, HA ;
Falkinham, JO ;
Wani, MC ;
Oberlies, NH .
JOURNAL OF NATURAL PRODUCTS, 2005, 68 (02) :173-178
[8]  
[Anonymous], 1972, ISOQUINOLINE ALKALOI
[9]  
[Anonymous], 1955, COLCHICINE AGR MED B
[10]   Novel B-ring modified allocolchicinoids of the NCME series:: Design, synthesis, antimicrotubule activity and cytotoxicity [J].
Bergemann, S ;
Brecht, R ;
Büttner, F ;
Guénard, D ;
Gust, R ;
Seitz, G ;
Stubbs, MT ;
Thoret, S .
BIOORGANIC & MEDICINAL CHEMISTRY, 2003, 11 (07) :1269-1281