All Stories

  1. Natural Products That Changed Society
  2. Targeting Toxins toward Tumors
  3. From Plant to Patient: Thapsigargin, a Tool for Understanding Natural Product Chemistry, Total Syntheses, Biosynthesis, Taxonomy, ATPases, Cell Death, and Drug Development
  4. Large Scale Conversion of Trilobolide into the Payload of Mipsagargin: 8-O-(12-Aminododecanoyl)-8-O-Debutanoylthapsigargin
  5. Cell death induced by the ER stressor thapsigargin involves death receptor 5, a non-autophagic function of MAP1LC3B, and distinct contributions from unfolded protein response components
  6. Missing Selectivity of Targeted 4β-Phorbol Prodrugs Expected to be Potential Chemotherapeutics
  7. Biosynthesis of tovarol and other sesquiterpenoids in Thapsia laciniata Rouy
  8. Nonlinear relationship between ER Ca2+ depletion versus induction of the unfolded protein response, autophagy inhibition, and cell death
  9. Phorbol Rearrangements
  10. Preparation of Enzyme-Activated Thapsigargin Prodrugs by Solid-Phase Synthesis
  11. A new flavonol glycoside and other flavonoids from the aerial parts of Taverniera aegyptiaca
  12. Cover Feature: LEGO-Inspired Drug Design: Unveiling a Class of Benzo[d ]thiazoles Containing a 3,4-Dihydroxyphenyl Moiety as Plasma Membrane H+ -ATPase Inhibitors (ChemMedChem 1/2018)
  13. LEGO-Inspired Drug Design: Unveiling a Class of Benzo[d ]thiazoles Containing a 3,4-Dihydroxyphenyl Moiety as Plasma Membrane H+ -ATPase Inhibitors
  14. Cover Feature: Difluoroacetic Acid as a New Reagent for Direct C−H Difluoromethylation of Heteroaromatic Compounds (Chem. Eur. J. 72/2017)
  15. Difluoroacetic Acid as a New Reagent for Direct C−H Difluoromethylation of Heteroaromatic Compounds
  16. Inhibition of the sarco/endoplasmic reticulum (ER) Ca2+-ATPase by thapsigargin analogs induces cell death via ER Ca2+depletion and the unfolded protein response
  17. Metformin, an Anthropogenic Contaminant of Seidlitzia rosmarinus Collected in a Desert Region near the Gulf of Aqaba, Sinai Peninsula
  18. Accelerating the Domestication of New Crops: Feasibility and Approaches
  19. Cranberry Juice and Combinations of Its Organic Acids Are Effective against Experimental Urinary Tract Infection
  20. Localization and in-Vivo Characterization of Thapsia garganica CYP76AE2 Indicates a Role in Thapsigargin Biosynthesis
  21. Structure/activity relationship of thapsigargin inhibition on the purified Golgi/secretory pathway Ca 2+ /Mn 2+ -transport ATPase (SPCA1a)
  22. Fusaric acid and analogues as Gram-negative bacterial quorum sensing inhibitors
  23. Demethoxycurcumin Is A Potent Inhibitor of P-Type ATPases from Diverse Kingdoms of Life
  24. Iminolactones as tools for inversion of the absolute configuration of α-amino acids and as inhibitors of cancer cell proliferation
  25. Meet Our Editorial Board Member
  26. Thapsigargin, origin, chemistry, structure-activity relationships and prodrug development
  27. Concise synthesis of thapsigargin from nortrilobolide
  28. Chemo- and Regioselective Functionalization of Nortrilobolide: Application for Semisynthesis of the Natural Product 2-Acetoxytrilobolide
  29. Iminolactones from Schizophyllum commune
  30. Targeting thapsigargin towards tumors
  31. Are we ready for back-to-nature crop breeding?
  32. Drugs and Drug Leads Based on Natural Products for Treatment and Prophylaxis of Malaria
  33. Contributors
  34. Differential effects of thapsigargin analogues on apoptosis of prostate cancer cells
  35. Serotonin transporter protein (SERT) and P-glycoprotein (P-gp) binding activity of montanine and coccinine from three species of Haemanthus L. (Amaryllidaceae)
  36. Water-Mediated Interactions Influence the Binding of Thapsigargin to Sarco/Endoplasmic Reticulum Calcium Adenosinetriphosphatase
  37. Guaianolide Sesquiterpenoids: Pharmacology and Biosynthesis
  38. Alkaloid analysis by high-performance liquid chromatography-solid phase extraction-nuclear magnetic resonance: New strategies going beyond the standard
  39. A Correction to the Research Article Titled: "Engineering a Prostate-Specific Membrane Antigen-Activated Tumor Endothelial Cell Prodrug for Cancer Therapy" by S. R. Denmeade, A. M. Mhaka, D. Marc Rosen, W. N. Brennen, S. Dalrymple, I. Dach, C. Olesen, ...
  40. Chalcone inhibitors of the NorA efflux pump in Staphylococcus aureus whole cells and enriched everted membrane vesicles
  41. Engineering a Prostate-Specific Membrane Antigen-Activated Tumor Endothelial Cell Prodrug for Cancer Therapy
  42. Novel inhibitory activity of the Staphylococcus aureus NorA efflux pump by a kaempferol rhamnoside isolated from Persea lingue Nees
  43. 6-O-Methylkrigeine, a new Amaryllidaceae alkaloid fromNerine huttoniaeSchönland
  44. Can phylogeny predict chemical diversity and potential medicinal activity of plants? A case study of amaryllidaceae
  45. Obituary – Professor Dr. Jerzy Jaroszewski
  46. Oleic and linoleic acids are active principles in Nigella sativa and stabilize an E2P conformation of the Na,K-ATPase. Fatty acids differentially regulate cardiac glycoside interaction with the pump
  47. Amaryllidaceae alkaloids from Rauhia multiflora (Kunth) Ravenna
  48. Thapsigargin affinity purification of intracellular P2A-type Ca2+ ATPases
  49. Amaryllidaceae alkaloids from the Australasian tribe Calostemmateae with acetylcholinesterase inhibitory activity
  50. Isolation of immunomodulatory triterpene acids from a standardized rose hip powder (Rosa canina L.)
  51. Characterization of anti-inflammatory triterpene acids from rose hip powder (Rosa canina L.)
  52. The pharmacophore of thapsigargin
  53. Elucidation of the topography of the thapsigargin binding site in the sarco-endoplasmic calcium ATPase
  54. Critical Roles of Hydrophobicity and Orientation of Side Chains for Inactivation of Sarcoplasmic Reticulum Ca2+-ATPase with Thapsigargin and Thapsigargin Analogs
  55. Structure–activity relationships of a small-molecule inhibitor of the PDZ domain of PICK1
  56. A Phenylpropanoid, a Slovenolide, Two Sulphur-Containing Germacranes and Ca2+-ATPase Inhibitors fromThapsia villosa
  57. 19α-Hydroxy-3-oxo-ursa-1,12-dien-28-oic acid, an antiplasmodial triterpenoid isolated fromCanthium multiflorum
  58. Amino acid containing thapsigargin analogues deplete androgen receptor protein via synthesis inhibition and induce the death of prostate cancer cells
  59. A Trojan Horse in Drug Development: Targeting of Thapsigargins Towards Prostate Cancer Cells
  60. Systemic 7-methylxanthine in retarding axial eye growth and myopia progression: a 36-month pilot study
  61. S-petasin and butterbur lactones dilate vessels through blockage of voltage gated calcium channels and block DNA synthesis
  62. Isolation of the MAO-inhibitor naringenin from Mentha aquatica L.
  63. Isolation of linoleic andα-linolenic acids as COX-1 and -2 inhibitors in rose hip
  64. A New Oxygenated Ursane Derivative from Canthium multiflorum
  65. Mild psychoactive constituents of Mentha aquatica L.
  66. Carroll rearrangement to construct the norneolignan skeleton
  67. A configurational and conformational study of aframodial and its diasteriomers via experimental and theoretical VA and VCD spectroscopies
  68. Prenylated acetophenones from Melicope obscura and Melicope obtusifolia ssp. obtusifolia var. arborea and their distribution in Rutaceae
  69. Isolation and characterization of pristimerin as the antiplasmodial and antileishmanial agent of Maytenus senegalensis (Lam.) Exell.
  70. Identification of Natural Products Using HPLC-SPE Combined with CapNMR
  71. Cytotoxic kurubasch aldehyde fromTrichilia emetica
  72. Psychotropic constituents of Mentha aquatica L.
  73. Cytotoxic phenylpropanoids and an additional thapsigargin analogue isolated from Thapsia garganica
  74. Ancistrocladinium A and B, the First N,C-Coupled Naphthyldihydroisoquinoline Alkaloids, from a Congolese Ancistrocladus Species
  75. Sesquiterpenes from Thapsia nitida var. meridionalis and Thapsia nitida var. nitida
  76. Ethnopharmacological evaluation of radal (leaves of Lomatia hirsuta) and isolation of 2-methoxyjuglone
  77. Identification and evaluation of Peruvian plants used to treat malaria and leishmaniasis
  78. Natural products as starting materials for development of second-generation SERCA inhibitors targeted towards prostate cancer cells
  79. Pharmacokinetics, biodistribution, and antitumor efficacy of a human glandular kallikrein 2 (hK2)-activated thapsigargin prodrug
  80. Antimalarial and Antiplasmodial Activities of Norneolignans. Syntheses and SAR
  81. Total Synthesis of Two Novel Subpicomolar Sarco/Endoplasmatic Reticulum Ca 2+ -ATPase Inhibitors Designed by an Analysis of the Binding Site of Thapsigargin
  82. Structure and Absolute Configuration of Nyasol and Hinokiresinol via Synthesis and Vibrational Circular Dichroism Spectroscopy
  83. Applying Linear Interaction Energy Method for Rational Design of Noncompetitive Allosteric Inhibitors of the Sarco- and Endoplasmic Reticulum Calcium-ATPase
  84. The Antiparasitic Compound Licochalcone A Is a Potent Echinocytogenic Agent That Modifies the Erythrocyte Membrane in the Concentration Range Where Antiplasmodial Activity Is Observed
  85. Tethered Lipids fromThapsiagarganica
  86. Synthesis of the thapsigargins
  87. Ancistrotanzanine C and Related 5,1‘- and 7,3‘-Coupled Naphthylisoquinoline Alkaloids fromAncistrocladustanzaniensis1
  88. Antiplasmodial constituents ofCajanus cajan
  89. Ancistrotanzanine A, the First 5,3‘-Coupled Naphthylisoquinoline Alkaloid, and Two Further, 5,8‘-Linked Related Compounds from the Newly Described SpeciesAncistrocladus tanzaniensis#,1
  90. Prostate-Specific Antigen-Activated Thapsigargin Prodrug as Targeted Therapy for Prostate Cancer
  91. An Antiinflammatory Galactolipid from Rose Hip (Rosacanina) that Inhibits Chemotaxis of Human Peripheral Blood Neutrophils in Vitro
  92. An Antiplasmodial Lignan fromEuterpeprecatoria
  93. Hydrophilic Carboxylic Acids and Iridoid Glycosides in the Juice of American and European Cranberries (Vaccinium macrocarpon and V. oxycoccos), Lingonberries (V. vitis-idaea), and Blueberries (V. myrtillus)
  94. Antiplasmodial Compounds fromCochlospermumtinctorium
  95. Antiplasmodial Activity of Labdanes from Aframomum latifolium and Aframomum sceptrum
  96. Incorporation of the CrossFire Beilstein Database into the Organic Chemistry Curriculum at the Royal Danish School of Pharmacy
  97. In Vitro Antimycobacterial and Antilegionella Activity of Licochalcone A from Chinese Licorice Roots
  98. Design, Synthesis, and Pharmacological Evaluation of Thapsigargin Analogues for Targeting Apoptosis to Prostatic Cancer Cells
  99. Inhibition of Fumarate Reductase inLeishmania major and L. donovani by Chalcones
  100. Absolute Configuration and Antiprotozoal Activity of Minquartynoic Acid
  101. A Simple and Efficient Separation of the Curcumins, the Antiprotozoal Constituents of Curcuma longa
  102. Thapsigargin analogues for targeting programmed death of androgen-Independent prostate cancer cells
  103. The antileishmanial activity of novel oxygenated chalcones and their mechanism of action
  104. ACTA, a fluorescent analogue of thapsigargin, is a potent inhibitor and a conformational probe of skeletal muscle Ca2+ -ATPase
  105. Antileishmanial Chalcones:  Statistical Design, Synthesis, and Three-Dimensional Quantitative Structure−Activity Relationship Analysis
  106. limonoids from Khaya senegalensis
  107. Colouring agents in yellow and white flowered papaver radicatum in Northern Greenland
  108. Modifications of the α,β-Double bond in chalcones only Marginally affect the antiprotozoal activities
  109. A tool coming of age: thapsigargin as an inhibitor of sarco-endoplasmic reticulum Ca2+-ATPases
  110. The Novel Oxygenated Chalcone, 2,4‐Dimethoxy‐4'‐Butoxychalcone, Exhibits Potent Activity against Human Malaria ParasitePlasmodium falciparumIn Vitro and Rodent ParasitesPlasmodium bergheiandPlasmodium yoeliiIn Vivo
  111. Antiprotozoal Compounds fromAsparagus africanus
  112. New Anti-HIV-1, Antimalarial, and Antifungal Compounds fromTerminalia bellerica
  113. Two New Antiprotozoal 5-Methylcoumarins fromVernonia brachycalyx
  114. Lewis or brønsted acid provoked rearrangements in ortho-(1,1-dimethylpropenyl)phenols
  115. Discovery of oxygentade chalcones as novel antimalarial agents
  116. Synthesis, isolation and identification of glucuronides and mercapturic acids of a novel antiparasitic agent, licochalcone A
  117. Isolation of an angiotensin converting enzyme (ACE) inhibitor from Olea europaea and Olea lancea
  118. Syntheses of 11-Hydroxylated Guaianolides.
  119. The antileishmanial agent licochalcone A interferes with the function of parasite mitochondria
  120. Synthesis of antiparasitic licorice chalcones
  121. Structure-Activity Relationships of Analogs of Thapsigargin Modified at O-11 and O-12
  122. Thapsigargin, a novel molecular probe for studying intracellular calcium release and storage
  123. Licochalcone A, a new antimalarial agent, inhibits in vitro growth of the human malaria parasite Plasmodium falciparum and protects mice from P. yoelii infection.
  124. Antileishmanial activity of licochalcone A in mice infected with Leishmania major and in hamsters infected with Leishmania donovani.
  125. Molluscicidal saponins from a zimbabwean strain of Phytolacca dodecandra
  126. Ca2+-ATPase inhibitory activity of a locked analogue of thapsigargin
  127. Selective Transformations of the Ca2+ Pump Inhibitor Thapsigargin.
  128. Derivatives of thapsigargin as probes of its binding site on endoplasmic reticulum Ca2+ATPase
  129. Licochalcone A, a novel antiparasitic agent with potent activity against human pathogenic protozoan species of Leishmania.
  130. Localization of the Acyl Groups in Proazulene Guaianolides from Thapsia transtagana and Thapsia garganica
  131. Molluscicidal saponins from Phytolacca dodecandra
  132. Calcium entry in Xenopus oocytes: effects of inositol trisphosphate, thapsigargin and DMSO
  133. The Molluscicidal Activity of Coumarins from Ethulia conyzoides and of Dicumarol
  134. Toxicodynamics of tumour promoters of mouse skin III. Specific binding of the tumour promoter thapsigargin as measured by the cold-acetone filter assay
  135. Comparison of the Effects of Thapsigargin and BAY K 8644 on Spontaneous Mechanical Activity in Rat Portal Vein and Contractile Responses of Rat Cardiac Muscle
  136. The Absolute and Relative Configuration of the Molluscicides Ethuliacoumarin A and Isoethuliacoumarin A.
  137. Thapsigargin-Induced Increase in Cytoplasmic Ca2+Concentration and Aldosterone Production in Rat Adrenal Glomerulosa Cells: Interaction with Potassium and Angiotensin-II
  138. Guaiane esters from Thapsia villosa
  139. Exciton Coupling in Circular Dichroic Spectroscopy as a Tool for Establishing the Absolute Configuration of alpha,beta-Unsaturated Esters of Allylic Alcohols.
  140. New Proazulene Guaianolides from Thapsia villosa
  141. Ca2+ influx in human T lymphocytes is induced independently of inositol phosphate production by mobilization of intracellular Ca2+ stores. A study with the Ca2+ endoplasmic reticulum-ATPase inhibitor thapsigargin
  142. Inositol trisphosphate and thapsigargin discriminate endoplasmic reticulum stores of calcium in rat brain
  143. Hydroindene sesquiterpenes from Thapsia villosa
  144. Thapsigargin, a novel molecular probe for studying intracellular calcium release and storage
  145. Effect of thapsigargin on cytoplasmic Ca2+ and proliferation of human lymphocytes in relation to AIDS
  146. Effect of thapsigargin on cytoplasmic Ca2+ and proliferation of human lymphocytes in relations to AIDS
  147. Analysis of the stimulative effect of thapsigargin, a non-TPA-type tumour promoter, on arachidonic acid metabolism in rat peritoneal macrophages
  148. Dimethyl sulfoxide decreases the fluorescence yield of the reaction between histamine and ortho-phthalaldehyde and may influence histamine release
  149. Interpretation of the NMR and Circular Dichroic Data of the Sesquiterpene Lactone Thapsigargin.
  150. Effects of Thapsigargin in Isolated Rat Thoracic Aorta
  151. A New Sesquiterpene from Laserpitium latifolium
  152. Stimulation of arachidonic acid metabolism in rat peritoneal macrophages by thapsigargin, a non-(12-O-tetradecanoylphorbol-13-acetate) (TPA)-type tumor promoter
  153. The inflammatory and tumor-promoting sesquiterpene lactone, thapsigargin, activates platelets by selective mobilization of calcium as shown by protein phosphorylations
  154. Natural Products and Drug Development, Alfred Benzon Symposium 20Edited by P. Krogsgaard-Larsen, S. Brogger Christensen, and Helmer Kofod
  155. Isorhamnetin3-(2,6-dirhamnosylgalactoside)-7-rhamnoside and 3-(6-rhamnosylgalactoside)-7-rhamnoside from Rhazya stricta
  156. Synergistic stimulation of histamine release from rat peritoneal mast cells by 12-O-tetradecanoylphorbol 13-acetate (TPA)-type and non-TPA-type tumor promoters
  157. Thapsigargin, a histamine secretagogue, is a non-12-O-tetradecanolphorbol-13-acetate (TPA) type tumor promoter in two-stage mouse skin carcinogenesis
  158. Structure of a Pro-1,4-dimethylazulene Guaianolide from Thapsia garganica L.
  159. Natural Products and Drug Development
  160. The ability of thapsigargin and thapsigargicin to activate cells involved in the inflammatory response
  161. Analogues of the Histamine Liberating Dihydroxysesquiterpene Lactone Thapsigargin. Synthesis, X-Ray Analysis and Chemistry.
  162. Atriplex nummularia, a Source for the Two Molluscicide Saponins: Hederagenin-3-O-β-D-Glucuronopyranoside and Calenduloside E
  163. Absolute configurations of the histamine liberating sesquiterpene lactones thapsigargin and trilobolide
  164. Structure of histamine releasing guaianolides from Thapsia species
  165. Determination of cyanogenic compounds by thin-layer chromatography. 1. A densitometric method for quantification of cyanogenic glycosides, employing enzyme preparations (.beta.-glucuronidase) from Helix pomatia and picrate-impregnated ion-exchange sheets
  166. Stereochemistry and carbon-13 nuclear magnetic resonance of the histamineliberating sesquiterpene lactone thapsigargin. A modification of Horeau's method
  167. Thapsigargin and thapsigargicin, two histamine liberating sesquiterpene lactones from Thapsia garganica. X-ray analysis of the 7,11-epoxide of thapsigargin
  168. 2-β-d-Glucopyranosyloxy-2-methylpropanol in Acacia sieberana var. woodii
  169. 1-β-vicianosyl-(S)-2-methylbutyrate, a 1-O-acylglycoside from Acacia sieberana var. Woodii
  170. Proacaciberin, A cyanogenic glycoside from Acacia sieberiana var. Woodii
  171. Structural elucidation and partial synthesis of 3-hydroxyheterodendrin, a cyanogenic glucoside from Acacia sieberiana var. woodii
  172. Preparations of deuterium labelled guvacine and isoguvacine
  173. Thapsigargin, constitution of a sesquiterpene lactone histamine liberator from thapsia garganica
  174. Muscimol Analogues. I. Syntheses of 4- and 8-Aminocyclohepteno[1,2-d]isoxazol-3-ols and 4-(3-Aminopropyl)-5-methyl-3-isoxazolol.
  175. Structural Analogues of GABA. A New Convenient Synthesis of Muscimol.
  176. Organic Hydroxylamine Derivatives. XIII. The Configurations of a Series of Stereoisomeric 3-Methoxy-5-acylisoxazole Ketoximes.
  177. Organic Hydroxylamine Derivatives. XII. Structural Analogues of gamma-Aminobutyric Acid (GABA) of the Isoxazole Enol-betaine Type. Synthesis of Some 3-Hydroxy-5-(1-aminoalkyl)isoxazole Zwitterions.
  178. Organic Hydroxylamine Derivatives. VIII. Structural Analogues of GABA of the Isoxazole Enol-Betaine Type. Synthesis of 5,6,7,8-Tetrahydro-4H-isoxazolo[3,4-d]azepin-3-ol Zwitterion and Some Derivatives.
  179. Conformational Analysis. VIII. Separation and PMR Spectra of Some 4-Oxo-1,3-dioxans Derived from Diastereoisomeric 3-Hydroxy-2-methylbutyric Acids.
  180. Organic Hydroxylamine Derivatives. VII. Isoxazolin-5-ones. An Investigation of a Reaction Sequence Previously Stated to Give 3-Hydroxyisoxazoles.