All Stories

  1. Synthesis and evaluation of an AZD2461 [18F]PET probe in non-human primates reveals the PARP-1 inhibitor to be non-blood-brain barrier penetrant
  2. TMEM97 and PGRMC1 do not mediate sigma-2 ligand-induced cell death
  3. Cell-proliferation imaging for monitoring response to CDK4/6 inhibition combined with endocrine-therapy in breast cancer: Comparison of [18F]FLT and [18F]ISO-1 PET/CT
  4. Selectivity of probes for PET imaging of dopamine D3 receptors
  5. Dopamine D3 receptor partial agonist LS-3-134 attenuates cocaine-motivated behaviors
  6. Sigma-2 Receptor/TMEM97 and PGRMC-1 Increase the Rate of Internalization of LDL by LDL Receptor through the Formation of a Ternary Complex
  7. Validation of gallbladder absorbed radiation dose reduction simulation: human dosimetry of [18F]fluortriopride
  8. Altering Nitrogen Heterocycles of AZD2461 Affords High Affinity Poly(ADP-ribose) Polymerase-1 Inhibitors with Decreased P-Glycoprotein Interactions
  9. Analogues of Arylamide Phenylpiperazine Ligands To Investigate the Factors Influencing D3 Dopamine Receptor Bitropic Binding and Receptor Subtype Selectivity
  10. Examination of Diazaspiro Cores as Piperazine Bioisosteres in the Olaparib Framework Shows Reduced DNA Damage and Cytotoxicity
  11. Alpha Synuclein Fibrils Contain Multiple Binding Sites for Small Molecules
  12. Chalcones and Five-Membered Heterocyclic Isosteres Bind to Alpha Synuclein Fibrils in Vitro
  13. A PET imaging agent for evaluating PARP-1 expression in ovarian cancer
  14. Open letter to journal editors on: International consensus radiochemistry nomenclature guidelines
  15. Design, synthesis, and in vitro evaluation of quinolinyl analogues for α-synuclein aggregation
  16. Rapid Cu-Catalyzed [211At]Astatination and [125I]Iodination of Boronic Esters at Room Temperature
  17. PET Imaging of Microglial Activation—Beyond Targeting TSPO
  18. Synthesis and pharmacological evaluation of 6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline derivatives as sigma-2 receptor ligands
  19. Copper Loading of Preformed Nanoparticles for PET-Imaging Applications
  20. Highly Selective Dopamine D3 Receptor Antagonists with Arylated Diazaspiro Alkane Cores
  21. Development of a Positron Emission Tomography Radiotracer for Imaging Elevated Levels of Superoxide in Neuroinflammation
  22. Inflammation and DNA damage: Probing pathways to cancer and neurodegeneration
  23. Challenges in the development of dopamine D2- and D3-selective radiotracers for PET imaging studies
  24. Small Molecule Receptor Ligands for PET Studies of the Central Nervous System—Focus on G Protein Coupled Receptors
  25. Bacterial infection imaging with [ 18 F]fluoropropyl-trimethoprim
  26. Sigma-2 ligands and PARP inhibitors synergistically trigger cell death in breast cancer cells
  27. The role of beta-arrestin2 in shaping fMRI BOLD responses to dopaminergic stimulation
  28. [ 18 F](2 S ,4 R )4-Fluoroglutamine PET Detects Glutamine Pool Size Changes in Triple-Negative Breast Cancer in Response to Glutaminase Inhibition
  29. Design and Investigation of a [18F]-Labeled Benzamide Derivative as a High Affinity Dual Sigma Receptor Subtype Radioligand for Prostate Tumor Imaging
  30. PARP-1 Expression Quantified by [18F]FluorThanatrace: A Biomarker of Response to PARP Inhibition Adjuvant to Radiation Therapy
  31. PET of Poly (ADP-Ribose) Polymerase Activity in Cancer: Preclinical Assessment and First In-Human Studies
  32. The Targeted SMAC Mimetic SW IV-134 is a strong enhancer of standard chemotherapy in pancreatic cancer
  33. A patient-derived-xenograft platform to study BRCA-deficient ovarian cancers
  34. The Evolution of the Sigma-2 (σ2) Receptor from Obscure Binding Site to Bona Fide Therapeutic Target
  35. Quantitative PET Reporter Gene Imaging with [ 11 C]Trimethoprim
  36. Iodinated benzimidazole PARP radiotracer for evaluating PARP1/2 expression in vitro and in vivo
  37. Comparative evaluation of 4 and 6-carbon spacer conformationally flexible tetrahydroisoquinolinyl benzamide analogues for imaging the sigma-2 receptor status of solid tumors
  38. Automation of the Radiosynthesis of Six Different 18F-labeled radiotracers on the AllinOne
  39. The effect of the sigma-1 receptor selective compound LS-1-137 on the DOI-induced head twitch response in mice
  40. 4-aroylpiperidines and 4-(α-hydroxyphenyl)piperidines as selective sigma-1 receptor ligands: synthesis, preliminary pharmacological evaluation and computational studies
  41. A Radiotracer Strategy to Quantify PARP-1 Expression In Vivo Provides a Biomarker That Can Enable Patient Selection for PARP Inhibitor Therapy
  42. Conjugation to the sigma-2 ligand SV119 overcomes uptake blockade and converts dm-Erastin into a potent pancreatic cancer therapeutic
  43. Novel Strategies for Breast Cancer Imaging: New Imaging Agents to Guide Treatment
  44. Molecular Probes for Imaging the Sigma-2 Receptor: In Vitro and In Vivo Imaging Studies
  45. Improved Automated Radiosynthesis of [11C]PBR28
  46. Automated radiochemical synthesis and biodistribution of [11C]l-α-acetylmethadol ([11C]LAAM)
  47. Characterization of [3H]LS‐3‐134, a novel arylamide phenylpiperazine D3 dopamine receptor selective radioligand
  48. Pharmacological modulation of abnormal involuntary DOI-induced head twitch response in male DBA/2J mice: I. Effects of D2/D3 and D2 dopamine receptor selective compounds
  49. Synthesis and Structure–Activity Relationship Studies of Conformationally Flexible Tetrahydroisoquinolinyl Triazole Carboxamide and Triazole Substituted Benzamide Analogues as σ2 Receptor Ligands
  50. Targeted pancreatic cancer therapy with the small molecule drug conjugate SW IV‐134
  51. Using SV119‐Gold Nanocage Conjugates to Eradicate Cancer Stem Cells Through a Combination of Photothermal and Chemo Therapies
  52. Radiosynthesis and in Vivo Evaluation of Two PET Radioligands for Imaging α-Synuclein
  53. Conjugation to a SMAC mimetic potentiates sigma-2 ligand induced tumor cell death in ovarian cancer
  54. Functional assays to define agonists and antagonists of the sigma-2 receptor
  55. Synthesis, [18F] radiolabeling, and evaluation of poly (ADP-ribose) polymerase-1 (PARP-1) inhibitors for in vivo imaging of PARP-1 using positron emission tomography
  56. Development of a PET radiotracer for non-invasive imaging of the reactive oxygen species, superoxide, in vivo
  57. Regulation of dopamine presynaptic markers and receptors in the striatum of DJ-1 and Pink1 knockout rats
  58. Quantitative Receptor-Based Imaging of Tumor Proliferation with the Sigma-2 Ligand [18F]ISO-1
  59. Fos expression in response to dopamine D3-preferring phenylpiperazine drugs given with and without cocaine
  60. The σ2 Receptor: A Novel Protein for the Imaging and Treatment of Cancer
  61. Evaluation of N-phenyl homopiperazine analogs as potential dopamine D3 receptor selective ligands
  62. Development of <sup>18</sup>F-Labeled PET Probes for Imaging Cell Proliferation
  63. Positron emission tomography imaging of dopamine D2 receptors using a highly selective radiolabeled D2 receptor partial agonist
  64. Binding of the Radioligand SIL23 to α-Synuclein Fibrils in Parkinson Disease Brain Tissue Establishes Feasibility and Screening Approaches for Developing a Parkinson Disease Imaging Agent
  65. Synthesis and in vitro pharmacological evaluation of indolyl carboxylic amide analogues as D3 dopamine receptor selective ligands
  66. The Effect of SV 293, a D2 Dopamine Receptor-Selective Antagonist, on D2 Receptor-Mediated GIRK Channel Activation and Adenylyl Cyclase Inhibition
  67. Dopamine D1, D2, D3 Receptors, Vesicular Monoamine Transporter Type-2 (VMAT2) and Dopamine Transporter (DAT) Densities in Aged Human Brain
  68. Highly efficient click labeling using 2-[18F]fluoroethyl azide and synthesis of an 18FN-hydroxysuccinimide ester as conjugation agent
  69. Comparison of the Binding and Functional Properties of Two Structurally Different D2 Dopamine Receptor Subtype Selective Compounds
  70. Synthesis, radiolabeling and initial in vivo evaluation of [11C]KSM-01 for imaging PPAR-α receptors
  71. Therapeutic targeting of pancreatic cancer utilizing sigma-2 ligands
  72. Exploration of ring size in a series of cyclic vicinal diamines with σ1 receptor affinity
  73. IC‐O3‐02: Development of a CAA‐specific amyloid imaging tracer
  74. Development of a cerebral amyloid angiopathy–specific amyloid imaging tracer
  75. Neuroprotective effects of high affinity sigma 1 receptor selective compounds
  76. No Differential Regulation of Dopamine Transporter (DAT) and Vesicular Monoamine Transporter 2 (VMAT2) Binding in a Primate Model of Parkinson Disease
  77. Synthesis and evaluation of 18F-labeled PPARγ antagonists
  78. SV119-gold nanocage conjugates: a new platform for targeting cancer cellsvia sigma-2 receptors
  79. Radiolabeled isatin binding to caspase-3 activation induced by anti-Fas antibody
  80. PET imaging for attention deficit preclinical drug testing in neurofibromatosis-1 mice
  81. N-Arylalkyl-2-azaadamantanes as cage-expanded polycarbocyclic sigma (σ) receptor ligands
  82. Synthesis and in vitro evaluation of new analogues as inhibitors for phosphodiesterase 10A
  83. Sleep deprivation differentially affects dopamine receptor subtypes in mouse striatum
  84. Identification of the PGRMC1 protein complex as the putative sigma-2 receptor binding site
  85. Effect of cyclosporin A on the uptake of D3-selective PET radiotracers in rat brain
  86. Synthesis and characterization of selective dopamine D2 receptor ligands using aripiprazole as the lead compound
  87. Sigma-2 Receptor as Potential Indicator of Stem Cell Differentiation
  88. Synthesis and evaluation of isatin analogs as caspase-3 inhibitors: Introduction of a hydrophilic group increases potency in a whole cell assay
  89. Endogenous dopamine (DA) competes with the binding of a radiolabeled D3 receptor partial agonist in vivo: A positron emission tomography study
  90. p-Acetoxybenzyl Bromide
  91. Radiosynthesis and in vivo evaluation of [11C]MP-10 as a PET probe for imaging PDE10A in rodent and non-human primate brain
  92. Synthesis and Pharmacological Evaluation of Fluorine-Containing D3 Dopamine Receptor Ligands
  93. Automated radiosynthesis of [11C]morphine for clinical investigation
  94. Resorufin analogs preferentially bind cerebrovascular amyloid: potential use as imaging ligands for cerebral amyloid angiopathy
  95. Radiosynthesis and biological evaluation of a promising σ2-receptor ligand radiolabeled with fluorine-18 or iodine-125 as a PET/SPECT probe for imaging breast cancer
  96. The novel sigma-2 receptor ligand SW43 stabilizes pancreas cancer progression in combination with gemcitabine
  97. Synthesis and Evaluation of 15-(4-(2-[18F]Fluoroethoxy)phenyl)pentadecanoic Acid: A Potential PET Tracer for Studying Myocardial Fatty Acid Metabolism
  98. Decreased striatal dopamine receptor binding in primary focal dystonia: A D2 or D3 defect?
  99. Subtype Selectivity of Dopamine Receptor Ligands: Insights from Structure and Ligand-Based Methods
  100. Synthesis and characterization of selective dopamine D2 receptor antagonists. 2. Azaindole, benzofuran, and benzothiophene analogs of L-741,626
  101. Carbon-11 labeled papaverine as a PET tracer for imaging PDE10A: radiosynthesis, in vitro and in vivo evaluation
  102. Synthesis andin VitroBiological Evaluation of Carbonyl Group-Containing Inhibitors of Vesicular Acetylcholine Transporter
  103. Radiochemical Synthesis, Rodent Biodistribution and Tumor Uptake, and Dosimetry Calculations of [11C] Methylated LY2181308
  104. Challenges for Developing PET Tracers: Isotopes, Chemistry, and Regulatory Aspects
  105. Evaluation of 5-ethynyl-2′-deoxyuridine staining as a sensitive and reliable method for studying cell proliferation in the adult nervous system
  106. [3H]4‐(dimethylamino)‐N‐(4‐(4‐(2‐methoxyphenyl)piperazin‐1‐yl) butyl)benzamide: A selective radioligand for dopamine D3 receptors. II. Quantitative analysis of dopamine D3 and D2 receptor density ratio...
  107. Cerebrospinal fluid tau and ptau 181 increase with cortical amyloid deposition in cognitively normal individuals: Implications for future clinical trials of Alzheimer's disease
  108. Using prepulse inhibition to detect functional D3 receptor antagonism: Effects of WC10 and WC44
  109. Comparison of radiolabeled isatin analogs for imaging apoptosis with positron emission tomography
  110. Docking and 3D-QSAR Studies on Isatin Sulfonamide Analogues as Caspase-3 Inhibitors
  111. [3H]4‐(Dimethylamino)‐N‐[4‐(4‐(2‐methoxyphenyl)piperazin‐ 1‐yl)butyl]benzamide, a selective radioligand for dopamine D3 receptors. I. In vitro characterization
  112. Evaluation of D2 and D3 dopamine receptor selective compounds on l-dopa-dependent abnormal involuntary movements in rats
  113. Synthesis and in Vitro Evaluation of Sulfonamide Isatin Michael Acceptors as Small Molecule Inhibitors of Caspase-6
  114. Sigma-2 receptor ligands potentiate conventional chemotherapies and improve survival in models of pancreatic adenocarcinoma
  115. Design and Synthesis of 2-Amino-4-methylpyridine Analogues as Inhibitors for Inducible Nitric Oxide Synthase and in Vivo Evaluation of [18F]6-(2-Fluoropropyl)-4-methyl-pyridin-2-amine as a Potential PET Tracer for Inducible Nitric Oxide Synt...
  116. Synthesis and in Vitro and in Vivo Evaluation of 18F-Labeled Positron Emission Tomography (PET) Ligands for Imaging the Vesicular Acetylcholine Transporter
  117. New N-substituted 9-azabicyclo[3.3.1]nonan-3α-yl phenylcarbamate analogs as σ2 receptor ligands: Synthesis, in vitro characterization, and evaluation as PET imaging and chemosensitization agents
  118. Preface
  119. PET Radiotracers for Imaging the Proliferative Status of Solid Tumors
  120. O3‐02–02: Update on the relationship between in vivo amyloid imaging with C‐PIB and CSF Aβ42
  121. QS306. A Pancreas Cancer Targeted Akt Inhibitor Induces Apoptosis
  122. P31. A Pancreas Cancer Targeted AkT Inhibitor Induces Apoptosis
  123. Selective sigma-2 ligands preferentially bind to pancreatic adenocarcinomas: applications in diagnostic imaging and therapy
  124. Isatin Sulfonamide Analogs Containing a Michael Addition Acceptor:  A New Class of Caspase 3/7 Inhibitors
  125. Fluorine-18-Labeled Benzamide Analogues for Imaging the σ2 Receptor Status of Solid Tumors with Positron Emission Tomography
  126. Imaging the proliferative status of tumors with PET
  127. Strategies for the Labeling of Halogen-Substituted Peroxisome Proliferator-Activated Receptor γ Ligands:  Potential Positron Emission Tomography and Single Photon Emission Computed Tomography Imaging Agents
  128. Synthesis and Binding Affinity of a Fluorine-Substituted Peroxisome Proliferator-Activated Gamma (PPARγ) Ligand as a Potential Positron Emission Tomography (PET) Imaging Agent
  129. IN VIVO IMAGING IN A MURINE MODEL OF GLIOBLASTOMA
  130. Synthesis of N-substituted 9-azabicyclo[3.3.1]nonan-3α-yl carbamate analogs as σ2 receptor ligands
  131. Synthesis and evaluation of a bromine-76-labeled PPARγ antagonist 2-bromo-5-nitro-N-phenylbenzamide
  132. Synthesis, radiolabeling, and in vivo evaluation of an 18F-labeled isatin analog for imaging caspase-3 activation in apoptosis
  133. PET imaging of dopamine D2 receptors during chronic cocaine self-administration in monkeys
  134. O3–01–07: Relationship between in vivo amyloid imaging with 11C–PIB and CSF Aβ42
  135. IC–P–054: Relationship between in vivo amyloid imaging with 11C–PIB and CSF Aβ42
  136. Inverse relation between in vivo amyloid imaging load and cerebrospinal fluid Aβ42 in humans
  137. Synthesis and characterization of selective dopamine D2 receptor antagonists
  138. Characterization of a novel iodinated sigma-2 receptor ligand as a cell proliferation marker
  139. N-Benzylisatin Sulfonamide Analogues as Potent Caspase-3 Inhibitors:  Synthesis, in Vitro Activity, and Molecular Modeling Studies
  140. [3H]N-[4-(3,4-dihydro-6,7-dimethoxyisoquinolin-2(1H)-yl)butyl]-2-methoxy-5-methylbenzamide: A novel sigma-2 receptor probe
  141. N‐[18F]4′‐fluorobenzylpiperidin‐4yl‐(2‐fluorophenyl) acetamide ([18F]FBFPA): A potential fluorine‐18 labeled PET radiotracer for imaging sigma‐1 receptors in the CNS
  142. Carbon-11 labeled σ2 receptor ligands for imaging breast cancer
  143. Synthesis and in vivo evaluation of [11C]PJ34, a potential radiotracer for imaging the role of PARP-1 in necrosis
  144. Bioluminescence Imaging of Transcription Factor Activity in the Lungs
  145. Synthesis and in vitro binding of N-phenyl piperazine analogs as potential dopamine D3 receptor ligands
  146. Evaluation of the Quantitative Capability of a High-Resolution Positron Emission Tomography Scanner for Small Animal Imaging
  147. P2-188 Labeling amyloid plaque-like structures by radioiodinated ligands in rhesus monkey brain
  148. Imaging Myocardium Enzymatic Pathways with Carbon-11 Radiotracers
  149. Conformationally-flexible benzamide analogues as dopamine D3 and σ2 receptor ligands
  150. Progress in Developing D3 Dopamine Receptor Ligands as Potential Therapeutic Agents for Neurological and Neuropsychiatric Disorders
  151. Synthesis of 2-(5-Bromo-2,3-dimethoxyphenyl)-5-(aminomethyl)-1H-pyrrole analogues and their binding affinities for dopamine D2, D3, and D4 receptors
  152. Cocaine- and food-maintained responding under a multiple schedule in rhesus monkeys: environmental context and the effects of a dopamine antagonist
  153. PET Radiotracers for Imaging the Proliferative Status of Breast Tumors
  154. Social dominance in monkeys: dopamine D2 receptors and cocaine self-administration
  155. Synthesis of 2-(2,3-dimethoxyphenyl)-4-(aminomethyl)imidazole analogues and their binding affinities for dopamine D2 and D3 receptors
  156. Synthesis and Structure−Activity Relationships of N-(1-Benzylpiperidin-4-yl)arylacetamide Analogues as Potent σ1 Receptor Ligands
  157. Preparation of a technetium‐99m SPECT agent for imaging the sigma‐2 receptor status of solid tumors
  158. Development of a Tc-99m labeled sigma-2 receptor-specific ligand as a potential breast tumor imaging agent
  159. Synthesis and Structure−Activity Relationships of Naphthamides as Dopamine D3 Receptor Ligands
  160. Morphine-induced spinal cholinergic activation: in vivo imaging with positron emission tomography
  161. Characterization of 125I‐IABN, a novel azabicyclononane benzamide selective for D2‐like dopamine receptors
  162. Characterization of125I-IABN, a novel azabicyclononane benzamide selective for D2-like dopamine receptors
  163. Cholinergic activity of aged rhesus monkeys revealed by positron emission tomography
  164. Fluorine-18-labeled tropane analogs for PET imaging studies of the dopamine transporter
  165. Hydroxylated Decahydroquinolines as Ligands for the Vesicular Acetylcholine Transporter:  Synthesis and Biological Evaluation
  166. Dopamine D2/D3 receptors modulate cocaine’s reinforcing and discriminative stimulus effects in rhesus monkeys
  167. The analgesic tropane analogue (±)-SM 21 has a high affinity for σ2 receptors
  168. In Vivo Imaging of the Spinal Cord Cholinergic System with PET
  169. AGE-RELATED CEREBRAL BLOOD FLOW RESPONSES DURING ISOFLURANE ANESTHESIA ASSESSED BY POSITRON EMISSION TOMOGRAPHY
  170. Synthesis and Quantitative Structure−Activity Relationships of N-(1-Benzylpiperidin-4-yl)phenylacetamides and Related Analogues as Potent and Selective σ1 Receptor Ligands
  171. Effect of social status on striatal dopamine D2 receptor binding characteristics in cynomolgus monkeys assessed with positron emission tomography
  172. Effect of social status on striatal dopamine D2 receptor binding characteristics in cynomolgus monkeys assessed with positron emission tomography
  173. N-Hydroxyalkyl Derivatives of 3β-Phenyltropane and 1-Methylspiro[1H-indoline-3,4‘-piperidine]:  Vesamicol Analogues with Affinity for Monoamine Transporters
  174. Use of Positron Emission Tomography to Study the Dynamics of Psychostimulant-Induced Dopamine Release
  175. Imaging of cholinergic terminals using the radiotracer [18F](+)-4-fluorobenzyltrozamicol: In vitro binding studies and positron emission tomography studies in nonhuman primates
  176. Social Stress, Depression, and Brain Dopamine in Female Cynomolgus Monkeys
  177. Comparison of two fluorine-18 labeled benzamide derivatives that bind reversibly to dopamine D2 receptors: In vitro binding studies and positron emission tomography
  178. Ibogaine possesses a selective affinity for σ2 receptors
  179. Vesamicol analogues as sigma ligands
  180. Pet imaging studies of dopamine D2 receptors: Comparison of [18F]N‐Methylspiperone; and the benzamide analogues [18F]MABN and [18F]MBP in baboon brain
  181. Fluorine-18 labeled benzamides for studying the dopamine D2 receptor with positron emission tomography
  182. The use of [18F]4-fluorobenzyl iodide (FBI) in PET radiotracer synthesis: Model alkylation studies and its application in the design of dopamine D1 and D2 receptor-based imaging agents
  183. Synthesis and in vivo evaluation of [18F]-N-(p-Nitrobenzyl)spiperone ([18F]PNBS) in rats
  184. Effect of N-alkylation on the affinities of analogs of spiperone for dopamine D2 and serotonin 5-HT2 receptors
  185. Mass spectral analysis diaminodithiol ligands used for the complexation of technetium‐99m
  186. Synthesis and biodistribution of a new class of 99mTc-labeled fatty acid analogs for myocardial imaging
  187. Antibodies with high affinity for spiroperidol—II. cross reactivity with iodobenzamide and domperidone
  188. Synthesis and chemical reactivity of c‐5 substituted 6,7‐bis‐(hydroxymethyl)‐1H‐pyrrolizine biscarbamate tumor inhibitors
  189. Synthesis, characterization and biodistribution of neutral and lipid-soluble 99mTc-PAT-HM and 99mTc-TMR for brain imaging
  190. Dopamine D-2 receptor imaging radiopharmaceuticals: synthesis, radiolabeling and in vitro binding of (R)-(+)- and (S)-(-)-3-iodo-2-hydroxy-6-methoxy-N-[(1-ethyl-2-pyrrolidinyl)methyl]benzamide
  191. Vinylogous carbinolamine tumor inhibitors. 21. Synthesis, chemical reactivity, and antileukemic activity of 5-substituted 6,7-bis(hydroxymethyl)pyrrolo[1,2-c]thiazole biscarbamates and the corresponding sulfoxides and sulfones
  192. Selective Reduction of Carboxylic Acid Esters in the Presence of a Five-Membered Cyclic Sulfone