Harald Greger

ORCID: 0000-0003-2614-7003
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Research Areas
  • Phytochemical compounds biological activities
  • Plant chemical constituents analysis
  • Chemical synthesis and alkaloids
  • Phytochemistry and Biological Activities
  • Sesquiterpenes and Asteraceae Studies
  • Essential Oils and Antimicrobial Activity
  • Advanced Synthetic Organic Chemistry
  • Traditional and Medicinal Uses of Annonaceae
  • Natural product bioactivities and synthesis
  • Alkaloids: synthesis and pharmacology
  • Plant Toxicity and Pharmacological Properties
  • Synthetic Organic Chemistry Methods
  • Plant Pathogens and Fungal Diseases
  • Herbal Medicine Research Studies
  • Insect Pest Control Strategies
  • Fungal Plant Pathogen Control
  • Synthesis of Organic Compounds
  • Biological Activity of Diterpenoids and Biflavonoids
  • Bioactive natural compounds
  • Plant biochemistry and biosynthesis
  • Fungal Biology and Applications
  • Synthesis and Biological Activity
  • Plant-derived Lignans Synthesis and Bioactivity
  • Analytical Chemistry and Chromatography
  • Quinazolinone synthesis and applications

University of Vienna
2010-2025

Chinese University of Hong Kong
2006-2010

Kasetsart University
2000-2009

Hong Kong Jockey Club
2006

Czech Academy of Sciences, Institute of Botany
1986-2004

University of Graz
1969-2004

FH Campus Wien
1988

Leiden University
1982

Technische Universität Berlin
1977

Antifungal testing of filamentous fungi generally suffers from incomparability results. In order to illustrate this problem, the polyacetylene falcarindiol and naphthoquinone juglone, two known antifungal natural products, were assayed in various dilution diffusion bioassays against three selected microfungi, Botrytis cinerea, Cladosporium herbarum Fusarium avenaceum. Broth microdilution, based on 96-well microtitre plate format, can be scored by direct biochemical methods. As examples,...

10.1002/(sici)1099-1565(200005/06)11:3<137::aid-pca514>3.0.co;2-i article EN Phytochemical Analysis 2000-05-01

Disablement of cell death programs in cancer cells contributes to drug resistance and some cases has been associated with altered translational control. As eukaryotic translation initiation factor 4E (eIF4E) cooperates c-Myc during lymphomagenesis, induces resistance, is a genetic modifier the rapamycin response, we have investigated effect dysregulation ribosome recruitment phase on tumor progression chemosensitivity. eIF4E subunit eIF4F, complex that stimulates by delivering DEAD-box RNA...

10.1172/jci34753 article EN Journal of Clinical Investigation 2008-06-01

Background Flavaglines are a family of natural products from the genus Aglaia that exhibit anti-cancer activity in vitro and vivo inhibit translation initiation. They have been shown to modulate eIF4A, DEAD-box RNA helicase subunit eukaryotic initiation factor (eIF) 4F complex, complex stimulates ribosome recruitment during One flavagline, silvestrol, is capable modulating chemosensitivity mechanism-based mouse model. Methodology/Principal Findings Among number flavagline members tested...

10.1371/journal.pone.0005223 article EN cc-by PLoS ONE 2009-04-28

Cyclotides are a unique class of ribosomally synthesized cysteine-rich miniproteins characterized by head-to-tail cyclized backbone and three conserved disulfide-bonds in knotted arrangement. Originally they were discovered the coffee-family plant Oldenlandia affinis (Rubiaceae) have since been identified several species violet, cucurbit, pea, potato, grass families. However, identification novel cyclotide-containing still is major challenge due to lack rapid accurate analytical workflow...

10.1002/bip.22328 article EN other-oa Biopolymers 2013-07-29

Fifteen new stilbenoids including 11 phenylbenzofurans, the stemofurans A-K (1-11), and four dihydrostilbenes, stilbostemins A (15), C (17), E (19), F (20), were isolated identified from a methanolic extract of Stemona collinsae roots together with five known derivatives, stilbenes pinosylvin (13) 4'-methylpinosylvin (14), B (16) D (18), dihydrophenanthrene racemosol (12) as well (+)-sesamin, coniferyl alcohol, stigmasterol. Bioautographic tests Cladosporium herbarum displayed antifungal...

10.1021/np0105073 article EN Journal of Natural Products 2002-05-11

Polyunsaturated alkamides isolated from Achillea species, Echinacea angustifolia DC., Anacyclus pyrethrum (L.) Link, and Aaronsohnia pubescens (Desf.) Bremer & Humphries, (Compositae) were shown to possess inhibitory activity in vitro cyclooxygenase (sheep seminal microsomes) 5-lipoxygenase (porcine leukocytes) assays. Activity appeared depend on the particular structure of alkamides.

10.1055/s-2006-959404 article EN Planta Medica 1994-02-01

On the basis of chronic feeding bioassays with neonate larvae Spodoptera littoralis reared on an artificial diet, methanolic leaf and root extracts from Stemona collinsae displayed very high insect toxicity compared to those two Aglaia species, a commercial Pyrethrum extract, azadirachtin, whereas S. tuberosa demonstrated low activity in roots no leaves. Beyond that, disk choice tests against fifth instar larvae, showed strong antifeedant activity, was characterized by remarkable repellency....

10.1021/jf0205615 article EN Journal of Agricultural and Food Chemistry 2002-09-24

Stemona alkaloids represent a unique class of natural products exclusively known from the three genera Stemona, Stichoneuron, and Croomia monocotyledonous family Stemonaceae. Structurally they are characterized by central pyrroloazepine core usually linked with two butyrolactone rings. The great diversity, comprising 215 derivatives, is created formation additional C–C linkages oxygen bridges together ring cleavages eliminations lactone Based on biosynthetic considerations can be grouped...

10.1007/s11101-019-09602-6 article EN cc-by Phytochemistry Reviews 2019-03-19

Seven new naturally occurring 3-butylisocoumarins were isolated and identified from lipophilic extracts of aerial as well underground organs: corfin (17) 3'-hydroxycorfin (18) the roots Chamaemelum mixtum (−)-(R)-2'-methoxydihydroartemidin (5), (+)-(S,R)-epoxyartemidin (6a), dracumerin (12), (+)-(R)-(E)-3'-hydroxyartemidin (13), capillarin isovalerate (20) various organs Artemisia dracunculus (tarragon). Furthermore, six known derivatives, artemidiol (7), (E/Z)-artemidin (11), (19),...

10.1021/np0301339 article EN Journal of Natural Products 2003-12-12

Twelve new derivatives of bisamides [piriferinol (5), edulimide (7)], lignans [lariciresinol acetat (10)], triterpenes [4-bis-norcycloartane-type (11a, 12a+b, 13a+b)], cyclopenta[b]benzofurans [pannellin (15), pannellin 1-O-acetate (16), 3'-methoxypannellin (17)], and an aromatic butyrolactone [aglalactone (18)] were isolated identified from lipophilic leaf, stem, root extracts Aglaia spp. elaeagnoidea, edulis, grandis, silvestris, tomentosa. Two (flavaglines), (15) displayed very strong...

10.1021/np9801965 article EN Journal of Natural Products 1998-10-20

Abstract: Sequences of the plastid DNA atp B/ rbc L intergenic spacer and rps16 intron from 23 genera 47 species Rutaceae were used to resolve phylogenetic relationships in subfamily Aurantioideae. According these, is monophyletic, but its classical subdivision into tribes Clauseneae Citreae only justified if genus Murraya s.s. (exclusive segregated as Bergera , e.g., koenigii M. siamensis ) Merrillia are transferred s.l. This conclusion also well supported by phytochemistry, demonstrating...

10.1055/s-2001-11747 article EN Plant Biology 2001-01-01

Eight flavaglines, six cyclopenta[b]benzofurans, a cyclopenta[bc]benzopyran, and benzo[b]oxepine, together with an aromatic butyrolactone were isolated from Aglaia odorata, A. elaeagnoidea, edulis (Meliaceae) tested against the three plant pathogens Pyricularia grisea, Fusarium avenaceum, Alternaria citri for antifungal properties. Using microdilution technique linked digital image analysis of germ tubes, benzofurans displayed strong activity, whereas benzopyran, benzoxepine, inactive at...

10.1021/jf990509h article EN Journal of Agricultural and Food Chemistry 2000-03-25
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