2017
DOI: 10.1039/c7ra03152a
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Recent progress in ergot alkaloid research

Abstract: Ergot alkaloids are a class of indole derivatives produced by the genera of Ascomycota includingClaviceps,Aspergillus,Penicillium, andEpichloë.

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Cited by 52 publications
(59 citation statements)
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“…An important risk factor associated with this disease is the high IOP, which is why therapy is based on IOP reduction. All ergot alkaloids have in common an indole-derived tetracyclic ring structure (ergoline) and, according to their structural features, the naturally occurring ergots are categorized into three main classes: amide- and peptide-like amide derivatives of d -lysergic acid, and the clavine alkaloids [ 27 ] ( Figure 1 ). The pharmacological profile of ergot alkaloids is linked to the structural similarity between d -lysergic acid-derived compounds and neurotransmitters like noradrenaline, dopamine, and serotonin [ 28 ].…”
Section: Role Of Ergot Alkaloids In Reducing Intraocular Pressurementioning
confidence: 99%
“…An important risk factor associated with this disease is the high IOP, which is why therapy is based on IOP reduction. All ergot alkaloids have in common an indole-derived tetracyclic ring structure (ergoline) and, according to their structural features, the naturally occurring ergots are categorized into three main classes: amide- and peptide-like amide derivatives of d -lysergic acid, and the clavine alkaloids [ 27 ] ( Figure 1 ). The pharmacological profile of ergot alkaloids is linked to the structural similarity between d -lysergic acid-derived compounds and neurotransmitters like noradrenaline, dopamine, and serotonin [ 28 ].…”
Section: Role Of Ergot Alkaloids In Reducing Intraocular Pressurementioning
confidence: 99%
“…Ergot Alkaloids: 2016 detection of 25 ergot alkaloids in cereal samples by LC-MS/MS [ 985 ]; comparison of ESI and APPI coupled with LC-MS for the analysis of ergot alkaloids [ 986 ]; HPLC-FLD method for detection of five ergot alkaloids (ergometrine, ergotamine, ergocornine, ergocrypine and ergocristine) in animal feed [ 987 ]; UHPLC-HRMS for screening of ergot alkaloids in animal feed [ 988 ]; determination of the bioactive alkaloids tabersonine, serpentine, vindoline, catharanthine, tryptamine, and vincamine in Apocynaceae plants (C. roseus and V. minor) by LC-MS/MS [ 989 ]; 2017 review [ 990 ]; MALDI-MSI for imaging distribution of alkaloids [ 991 ]; review [ 992 ]; determination of three new ergot alkaloids by HRMS [ 993 ]; determination of the total ergot alkaloids in rye using HPTLC-FLD [ 994 ]; response surface methodology for the identification, screening and optimization of fermentation factors to produce ergot alkaloids [ 995 ]; identification of a new species by molecular and ergot alkaloid profile analysis [ 996 ]; identification of alpha-CPA by UHPLC Triple-TOF HRMS [ 997 ]; NIR hyperspectral imaging for the detection of ergot bodies in cereal flour [ 998 ]; 2018 LAESI-MS for detection of ergot alkaloids [ 999 ]; testing of 122 samples of rye grains harvested in three different regions of Poland in 2016 and 2017 for ergot and its alkaloids [ 1000 ]; a total ergot alkaloid EIA compared with HPLC-FLD for the determination of total ergot alkaloids [ 1001 ]; multi-laboratory study to determine applicability of HPLC-FLD and HPLC-MS/MS for the determination of ergot alkaloids in rye-containing breads [ 1002 ]; review [ 1003 ]; UHPLC-FLD method for the quantification of the six major ergot alkaloids and their corresponding epimers [ 1004 ]; ergot alkaloids determination using spectrophotometry and TLC [ 1005 ]; review of IR spectroscopy for the detection of ergot alkaloids [ 1006 ]; 2019 protocol introducing lysergic acid diethylamide (LSD) for internal standardization of the analysis of ergot alkaloids by LC-FLD [ 1007 ]; 2D LC-MS/MS method for the simultaneous determination of 350 pesticides, 16 mycotoxins, 6 ergot alkaloids as well as the growth regulators Chlormequat and Mepiqua [ 1008 ]; NIR and ATR-FT/MIR spectroscopy for the determination of major ergot alkaloids [ 1009 ].…”
Section: Routine and Improved Analyses Of Abused Substancesmentioning
confidence: 99%
“…To further improve expression, one can consider cofactor regeneration, the use of chaperones to prevent protein mis-folding, to improve protein export, and to overcome feedback inhibition from product formation. 71 The biosynthetic pathways of clavine-type alkaloids or Dlysergic acid from the branch point chanoclavine-I aldehyde in different species have been described in detail elsewhere 72 . E. coli HE system has been used for characterizing genes from the ergot alkaloid biosynthetic gene cluster of Penicillium roqueforti FM164.…”
Section: Host Organism: Escherichia Colimentioning
confidence: 99%