All Stories

  1. Development of β-lactams since 1986. Commentary on The discovery of penicillin and cephalosporins by Sydney Selwyn
  2. Drugs That Changed Society: Microtubule-Targeting Agents Belonging to Taxanoids, Macrolides and Non-Ribosomal Peptides
  3. Validation of anti-malarial leads from natural products and traditional medicine for treatment of malaria
  4. Mipsagargin: The Beginning—Not the End—of Thapsigargin Prodrug-Based Cancer Therapeutics
  5. Drugs That Changed Society: History and Current Status of the Early Antibiotics: Salvarsan, Sulfonamides, and β-Lactams
  6. Natural Products That Changed Society
  7. Targeting Toxins toward Tumors
  8. From Plant to Patient: Thapsigargin, a Tool for Understanding Natural Product Chemistry, Total Syntheses, Biosynthesis, Taxonomy, ATPases, Cell Death, and Drug Development
  9. Large Scale Conversion of Trilobolide into the Payload of Mipsagargin: 8-O-(12-Aminododecanoyl)-8-O-Debutanoylthapsigargin
  10. 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
  11. Missing Selectivity of Targeted 4β-Phorbol Prodrugs Expected to be Potential Chemotherapeutics
  12. Biosynthesis of tovarol and other sesquiterpenoids in Thapsia laciniata Rouy
  13. Nonlinear relationship between ER Ca2+ depletion versus induction of the unfolded protein response, autophagy inhibition, and cell death
  14. Phorbol Rearrangements
  15. Preparation of Enzyme-Activated Thapsigargin Prodrugs by Solid-Phase Synthesis
  16. A new flavonol glycoside and other flavonoids from the aerial parts of Taverniera aegyptiaca
  17. 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)
  18. LEGO-Inspired Drug Design: Unveiling a Class of Benzo[d ]thiazoles Containing a 3,4-Dihydroxyphenyl Moiety as Plasma Membrane H+ -ATPase Inhibitors
  19. Cover Feature: Difluoroacetic Acid as a New Reagent for Direct C−H Difluoromethylation of Heteroaromatic Compounds (Chem. Eur. J. 72/2017)
  20. Difluoroacetic Acid as a New Reagent for Direct C−H Difluoromethylation of Heteroaromatic Compounds
  21. Inhibition of the sarco/endoplasmic reticulum (ER) Ca2+-ATPase by thapsigargin analogs induces cell death via ER Ca2+depletion and the unfolded protein response
  22. Metformin, an Anthropogenic Contaminant of Seidlitzia rosmarinus Collected in a Desert Region near the Gulf of Aqaba, Sinai Peninsula
  23. Accelerating the Domestication of New Crops: Feasibility and Approaches
  24. Cranberry Juice and Combinations of Its Organic Acids Are Effective against Experimental Urinary Tract Infection
  25. Localization and in-Vivo Characterization of Thapsia garganica CYP76AE2 Indicates a Role in Thapsigargin Biosynthesis
  26. Structure/activity relationship of thapsigargin inhibition on the purified Golgi/secretory pathway Ca 2+ /Mn 2+ -transport ATPase (SPCA1a)
  27. Fusaric acid and analogues as Gram-negative bacterial quorum sensing inhibitors
  28. Demethoxycurcumin Is A Potent Inhibitor of P-Type ATPases from Diverse Kingdoms of Life
  29. Iminolactones as tools for inversion of the absolute configuration of α-amino acids and as inhibitors of cancer cell proliferation
  30. Meet Our Editorial Board Member
  31. Thapsigargin, origin, chemistry, structure-activity relationships and prodrug development
  32. Concise synthesis of thapsigargin from nortrilobolide
  33. Chemo- and Regioselective Functionalization of Nortrilobolide: Application for Semisynthesis of the Natural Product 2-Acetoxytrilobolide
  34. Iminolactones from Schizophyllum commune
  35. Targeting thapsigargin towards tumors
  36. Are we ready for back-to-nature crop breeding?
  37. Drugs and Drug Leads Based on Natural Products for Treatment and Prophylaxis of Malaria
  38. Contributors
  39. Differential effects of thapsigargin analogues on apoptosis of prostate cancer cells
  40. Serotonin transporter protein (SERT) and P-glycoprotein (P-gp) binding activity of montanine and coccinine from three species of Haemanthus L. (Amaryllidaceae)
  41. Water-Mediated Interactions Influence the Binding of Thapsigargin to Sarco/Endoplasmic Reticulum Calcium Adenosinetriphosphatase
  42. Guaianolide Sesquiterpenoids: Pharmacology and Biosynthesis
  43. Alkaloid analysis by high-performance liquid chromatography-solid phase extraction-nuclear magnetic resonance: New strategies going beyond the standard
  44. 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, ...
  45. Chalcone inhibitors of the NorA efflux pump in Staphylococcus aureus whole cells and enriched everted membrane vesicles
  46. Engineering a Prostate-Specific Membrane Antigen-Activated Tumor Endothelial Cell Prodrug for Cancer Therapy
  47. Novel inhibitory activity of the Staphylococcus aureus NorA efflux pump by a kaempferol rhamnoside isolated from Persea lingue Nees
  48. 6-O-Methylkrigeine, a new Amaryllidaceae alkaloid fromNerine huttoniaeSchönland
  49. Can phylogeny predict chemical diversity and potential medicinal activity of plants? A case study of amaryllidaceae
  50. Obituary – Professor Dr. Jerzy Jaroszewski
  51. 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
  52. Amaryllidaceae alkaloids from Rauhia multiflora (Kunth) Ravenna
  53. Thapsigargin affinity purification of intracellular P2A-type Ca2+ ATPases
  54. Amaryllidaceae alkaloids from the Australasian tribe Calostemmateae with acetylcholinesterase inhibitory activity
  55. Isolation of immunomodulatory triterpene acids from a standardized rose hip powder (Rosa canina L.)
  56. Characterization of anti-inflammatory triterpene acids from rose hip powder (Rosa canina L.)
  57. The pharmacophore of thapsigargin
  58. Elucidation of the topography of the thapsigargin binding site in the sarco-endoplasmic calcium ATPase
  59. Critical Roles of Hydrophobicity and Orientation of Side Chains for Inactivation of Sarcoplasmic Reticulum Ca2+-ATPase with Thapsigargin and Thapsigargin Analogs
  60. Structure–activity relationships of a small-molecule inhibitor of the PDZ domain of PICK1
  61. A Phenylpropanoid, a Slovenolide, Two Sulphur-Containing Germacranes and Ca2+-ATPase Inhibitors fromThapsia villosa
  62. 19α-Hydroxy-3-oxo-ursa-1,12-dien-28-oic acid, an antiplasmodial triterpenoid isolated fromCanthium multiflorum
  63. Amino acid containing thapsigargin analogues deplete androgen receptor protein via synthesis inhibition and induce the death of prostate cancer cells
  64. A Trojan Horse in Drug Development: Targeting of Thapsigargins Towards Prostate Cancer Cells
  65. Systemic 7-methylxanthine in retarding axial eye growth and myopia progression: a 36-month pilot study
  66. S-petasin and butterbur lactones dilate vessels through blockage of voltage gated calcium channels and block DNA synthesis
  67. Isolation of the MAO-inhibitor naringenin from Mentha aquatica L.
  68. Isolation of linoleic andα-linolenic acids as COX-1 and -2 inhibitors in rose hip
  69. A New Oxygenated Ursane Derivative from Canthium multiflorum
  70. Mild psychoactive constituents of Mentha aquatica L.
  71. Carroll rearrangement to construct the norneolignan skeleton
  72. A configurational and conformational study of aframodial and its diasteriomers via experimental and theoretical VA and VCD spectroscopies
  73. Prenylated acetophenones from Melicope obscura and Melicope obtusifolia ssp. obtusifolia var. arborea and their distribution in Rutaceae
  74. Isolation and characterization of pristimerin as the antiplasmodial and antileishmanial agent of Maytenus senegalensis (Lam.) Exell.
  75. Identification of Natural Products Using HPLC-SPE Combined with CapNMR
  76. Cytotoxic kurubasch aldehyde fromTrichilia emetica
  77. Psychotropic constituents of Mentha aquatica L.
  78. Cytotoxic phenylpropanoids and an additional thapsigargin analogue isolated from Thapsia garganica
  79. Ancistrocladinium A and B, the First N,C-Coupled Naphthyldihydroisoquinoline Alkaloids, from a Congolese Ancistrocladus Species
  80. Sesquiterpenes from Thapsia nitida var. meridionalis and Thapsia nitida var. nitida
  81. Ethnopharmacological evaluation of radal (leaves of Lomatia hirsuta) and isolation of 2-methoxyjuglone
  82. Identification and evaluation of Peruvian plants used to treat malaria and leishmaniasis
  83. Natural products as starting materials for development of second-generation SERCA inhibitors targeted towards prostate cancer cells
  84. Pharmacokinetics, biodistribution, and antitumor efficacy of a human glandular kallikrein 2 (hK2)-activated thapsigargin prodrug
  85. Antimalarial and Antiplasmodial Activities of Norneolignans. Syntheses and SAR
  86. Total Synthesis of Two Novel Subpicomolar Sarco/Endoplasmatic Reticulum Ca 2+ -ATPase Inhibitors Designed by an Analysis of the Binding Site of Thapsigargin
  87. Structure and Absolute Configuration of Nyasol and Hinokiresinol via Synthesis and Vibrational Circular Dichroism Spectroscopy
  88. Applying Linear Interaction Energy Method for Rational Design of Noncompetitive Allosteric Inhibitors of the Sarco- and Endoplasmic Reticulum Calcium-ATPase
  89. The Antiparasitic Compound Licochalcone A Is a Potent Echinocytogenic Agent That Modifies the Erythrocyte Membrane in the Concentration Range Where Antiplasmodial Activity Is Observed
  90. Tethered Lipids fromThapsiagarganica
  91. Synthesis of the thapsigargins
  92. Ancistrotanzanine C and Related 5,1‘- and 7,3‘-Coupled Naphthylisoquinoline Alkaloids fromAncistrocladustanzaniensis1
  93. Antiplasmodial constituents ofCajanus cajan
  94. Ancistrotanzanine A, the First 5,3‘-Coupled Naphthylisoquinoline Alkaloid, and Two Further, 5,8‘-Linked Related Compounds from the Newly Described SpeciesAncistrocladus tanzaniensis#,1
  95. Prostate-Specific Antigen-Activated Thapsigargin Prodrug as Targeted Therapy for Prostate Cancer
  96. An Antiinflammatory Galactolipid from Rose Hip (Rosacanina) that Inhibits Chemotaxis of Human Peripheral Blood Neutrophils in Vitro
  97. An Antiplasmodial Lignan fromEuterpeprecatoria
  98. 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)
  99. Antiplasmodial Compounds fromCochlospermumtinctorium
  100. Antiplasmodial Activity of Labdanes from Aframomum latifolium and Aframomum sceptrum
  101. Incorporation of the CrossFire Beilstein Database into the Organic Chemistry Curriculum at the Royal Danish School of Pharmacy
  102. In Vitro Antimycobacterial and Antilegionella Activity of Licochalcone A from Chinese Licorice Roots
  103. Design, Synthesis, and Pharmacological Evaluation of Thapsigargin Analogues for Targeting Apoptosis to Prostatic Cancer Cells
  104. Inhibition of Fumarate Reductase inLeishmania major and L. donovani by Chalcones
  105. Absolute Configuration and Antiprotozoal Activity of Minquartynoic Acid
  106. A Simple and Efficient Separation of the Curcumins, the Antiprotozoal Constituents of Curcuma longa
  107. Thapsigargin analogues for targeting programmed death of androgen-Independent prostate cancer cells
  108. The antileishmanial activity of novel oxygenated chalcones and their mechanism of action
  109. ACTA, a fluorescent analogue of thapsigargin, is a potent inhibitor and a conformational probe of skeletal muscle Ca2+ -ATPase
  110. Antileishmanial Chalcones:  Statistical Design, Synthesis, and Three-Dimensional Quantitative Structure−Activity Relationship Analysis
  111. limonoids from Khaya senegalensis
  112. Colouring agents in yellow and white flowered papaver radicatum in Northern Greenland
  113. Modifications of the α,β-Double bond in chalcones only Marginally affect the antiprotozoal activities
  114. A tool coming of age: thapsigargin as an inhibitor of sarco-endoplasmic reticulum Ca2+-ATPases
  115. The Novel Oxygenated Chalcone, 2,4‐Dimethoxy‐4'‐Butoxychalcone, Exhibits Potent Activity against Human Malaria ParasitePlasmodium falciparumIn Vitro and Rodent ParasitesPlasmodium bergheiandPlasmodium yoeliiIn Vivo
  116. Antiprotozoal Compounds fromAsparagus africanus
  117. New Anti-HIV-1, Antimalarial, and Antifungal Compounds fromTerminalia bellerica
  118. Two New Antiprotozoal 5-Methylcoumarins fromVernonia brachycalyx
  119. Lewis or brønsted acid provoked rearrangements in ortho-(1,1-dimethylpropenyl)phenols
  120. Discovery of oxygentade chalcones as novel antimalarial agents
  121. Synthesis, isolation and identification of glucuronides and mercapturic acids of a novel antiparasitic agent, licochalcone A
  122. Isolation of an angiotensin converting enzyme (ACE) inhibitor from Olea europaea and Olea lancea
  123. Syntheses of 11-Hydroxylated Guaianolides.
  124. The antileishmanial agent licochalcone A interferes with the function of parasite mitochondria
  125. Synthesis of antiparasitic licorice chalcones
  126. Structure-Activity Relationships of Analogs of Thapsigargin Modified at O-11 and O-12
  127. Thapsigargin, a novel molecular probe for studying intracellular calcium release and storage
  128. Licochalcone A, a new antimalarial agent, inhibits in vitro growth of the human malaria parasite Plasmodium falciparum and protects mice from P. yoelii infection.
  129. Antileishmanial activity of licochalcone A in mice infected with Leishmania major and in hamsters infected with Leishmania donovani.
  130. Molluscicidal saponins from a zimbabwean strain of Phytolacca dodecandra
  131. Ca2+-ATPase inhibitory activity of a locked analogue of thapsigargin
  132. Selective Transformations of the Ca2+ Pump Inhibitor Thapsigargin.
  133. Derivatives of thapsigargin as probes of its binding site on endoplasmic reticulum Ca2+ATPase
  134. Licochalcone A, a novel antiparasitic agent with potent activity against human pathogenic protozoan species of Leishmania.
  135. Localization of the Acyl Groups in Proazulene Guaianolides from Thapsia transtagana and Thapsia garganica
  136. Molluscicidal saponins from Phytolacca dodecandra
  137. Calcium entry in Xenopus oocytes: effects of inositol trisphosphate, thapsigargin and DMSO
  138. The Molluscicidal Activity of Coumarins from Ethulia conyzoides and of Dicumarol
  139. Toxicodynamics of tumour promoters of mouse skin III. Specific binding of the tumour promoter thapsigargin as measured by the cold-acetone filter assay
  140. 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
  141. The Absolute and Relative Configuration of the Molluscicides Ethuliacoumarin A and Isoethuliacoumarin A.
  142. Thapsigargin-Induced Increase in Cytoplasmic Ca2+Concentration and Aldosterone Production in Rat Adrenal Glomerulosa Cells: Interaction with Potassium and Angiotensin-II
  143. Guaiane esters from Thapsia villosa
  144. Exciton Coupling in Circular Dichroic Spectroscopy as a Tool for Establishing the Absolute Configuration of alpha,beta-Unsaturated Esters of Allylic Alcohols.
  145. New Proazulene Guaianolides from Thapsia villosa
  146. 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
  147. Inositol trisphosphate and thapsigargin discriminate endoplasmic reticulum stores of calcium in rat brain
  148. Hydroindene sesquiterpenes from Thapsia villosa
  149. Thapsigargin, a novel molecular probe for studying intracellular calcium release and storage
  150. Effect of thapsigargin on cytoplasmic Ca2+ and proliferation of human lymphocytes in relation to AIDS
  151. Effect of thapsigargin on cytoplasmic Ca2+ and proliferation of human lymphocytes in relations to AIDS
  152. Analysis of the stimulative effect of thapsigargin, a non-TPA-type tumour promoter, on arachidonic acid metabolism in rat peritoneal macrophages
  153. Dimethyl sulfoxide decreases the fluorescence yield of the reaction between histamine and ortho-phthalaldehyde and may influence histamine release
  154. Interpretation of the NMR and Circular Dichroic Data of the Sesquiterpene Lactone Thapsigargin.
  155. Effects of Thapsigargin in Isolated Rat Thoracic Aorta
  156. A New Sesquiterpene from Laserpitium latifolium
  157. Stimulation of arachidonic acid metabolism in rat peritoneal macrophages by thapsigargin, a non-(12-O-tetradecanoylphorbol-13-acetate) (TPA)-type tumor promoter
  158. The inflammatory and tumor-promoting sesquiterpene lactone, thapsigargin, activates platelets by selective mobilization of calcium as shown by protein phosphorylations
  159. Natural Products and Drug Development, Alfred Benzon Symposium 20Edited by P. Krogsgaard-Larsen, S. Brogger Christensen, and Helmer Kofod
  160. Isorhamnetin3-(2,6-dirhamnosylgalactoside)-7-rhamnoside and 3-(6-rhamnosylgalactoside)-7-rhamnoside from Rhazya stricta
  161. Synergistic stimulation of histamine release from rat peritoneal mast cells by 12-O-tetradecanoylphorbol 13-acetate (TPA)-type and non-TPA-type tumor promoters
  162. Thapsigargin, a histamine secretagogue, is a non-12-O-tetradecanolphorbol-13-acetate (TPA) type tumor promoter in two-stage mouse skin carcinogenesis
  163. Structure of a Pro-1,4-dimethylazulene Guaianolide from Thapsia garganica L.
  164. Natural Products and Drug Development
  165. The ability of thapsigargin and thapsigargicin to activate cells involved in the inflammatory response
  166. Analogues of the Histamine Liberating Dihydroxysesquiterpene Lactone Thapsigargin. Synthesis, X-Ray Analysis and Chemistry.
  167. Atriplex nummularia, a Source for the Two Molluscicide Saponins: Hederagenin-3-O-β-D-Glucuronopyranoside and Calenduloside E
  168. Absolute configurations of the histamine liberating sesquiterpene lactones thapsigargin and trilobolide
  169. Structure of histamine releasing guaianolides from Thapsia species
  170. 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
  171. Stereochemistry and carbon-13 nuclear magnetic resonance of the histamineliberating sesquiterpene lactone thapsigargin. A modification of Horeau's method
  172. Thapsigargin and thapsigargicin, two histamine liberating sesquiterpene lactones from Thapsia garganica. X-ray analysis of the 7,11-epoxide of thapsigargin
  173. 2-β-d-Glucopyranosyloxy-2-methylpropanol in Acacia sieberana var. woodii
  174. 1-β-vicianosyl-(S)-2-methylbutyrate, a 1-O-acylglycoside from Acacia sieberana var. Woodii
  175. Proacaciberin, A cyanogenic glycoside from Acacia sieberiana var. Woodii
  176. Structural elucidation and partial synthesis of 3-hydroxyheterodendrin, a cyanogenic glucoside from Acacia sieberiana var. woodii
  177. Preparations of deuterium labelled guvacine and isoguvacine
  178. Thapsigargin, constitution of a sesquiterpene lactone histamine liberator from thapsia garganica
  179. Muscimol Analogues. I. Syntheses of 4- and 8-Aminocyclohepteno[1,2-d]isoxazol-3-ols and 4-(3-Aminopropyl)-5-methyl-3-isoxazolol.
  180. Structural Analogues of GABA. A New Convenient Synthesis of Muscimol.
  181. Organic Hydroxylamine Derivatives. XIII. The Configurations of a Series of Stereoisomeric 3-Methoxy-5-acylisoxazole Ketoximes.
  182. 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.
  183. 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.
  184. Conformational Analysis. VIII. Separation and PMR Spectra of Some 4-Oxo-1,3-dioxans Derived from Diastereoisomeric 3-Hydroxy-2-methylbutyric Acids.
  185. Organic Hydroxylamine Derivatives. VII. Isoxazolin-5-ones. An Investigation of a Reaction Sequence Previously Stated to Give 3-Hydroxyisoxazoles.