about
A Clickable Analogue of Ketamine Retains NMDA Receptor Activity, Psychoactivity, and Accumulates in Neurons.Thiolene and SIFEL-based Microfluidic Platforms for Liquid-Liquid Extraction.[18F]- and [11C]-labeled N-benzyl-isatin sulfonamide analogues as PET tracers for apoptosis: synthesis, radiolabeling mechanism, and in vivo imaging study of apoptosis in Fas-treated mice using [11C]WC-98.Development of a microfluidic "click chip" incorporating an immobilized Cu(I) catalystSynthesis and characterization of the copper(II) complexes of new N2S2-donor macrocyclic ligands: synthesis and in vivo evaluation of the (64)Cu complexes.Neurosteroid analogues. 17. Inverted binding orientations of androsterone enantiomers at the steroid potentiation site on γ-aminobutyric acid type A receptorsMicrofluidic radiolabeling of biomolecules with PET radiometals.Comparison of the binding and functional properties of two structurally different D2 dopamine receptor subtype selective compounds.QSAR studies of copper azamacrocycles and thiosemicarbazones: MM3 parameter development and prediction of biological properties.Evaluation of N-phenyl homopiperazine analogs as potential dopamine D3 receptor selective ligands.Mutations of the GABA-A receptor alpha1 subunit M1 domain reveal unexpected complexity for modulation by neuroactive steroids.Triazine-based tool box for developing peptidic PET imaging probes: syntheses, microfluidic radiolabeling, and structure-activity evaluationBitropic D3 Dopamine Receptor Selective Compounds as Potential Antipsychotics."Click Chip" Conjugation of Bifunctional Chelators to Biomolecules.A digital revolution in radiosynthesis.Quantitation and visualization of tumor-specific T cells in the secondary lymphoid organs during and after tumor elimination by PET.Synthesis, pharmacological evaluation and molecular modeling studies of triazole containing dopamine D3 receptor ligands.Microfluidic labeling of biomolecules with radiometals for use in nuclear medicine.Molecular modeling of bifunctional chelate peptide conjugates. 1. Copper and indium parameters for the AMBER force field.Synthesis and characterization of racemic mixture and meso isomers of bis(trans-2-aminocyclohexyl)aminepentaacetic acid and the stabilities of their Gd(III) complexes.Regioselective N-substitution of cyclen with two different alkyl groups: synthesis of all possible isomers.Preparation of 66Ga- and 68Ga-labeled Ga(III)-deferoxamine-folate as potential folate-receptor-targeted PET radiopharmaceuticals.Use of binding energy in comparative molecular field analysis of isoform selective estrogen receptor ligands.Comparative in vivo behavior studies of cyclen-based copper-64 complexes: regioselective synthesis, X-ray structure, radiochemistry, log P, and biodistribution.A potential Dubin-Johnson syndrome imaging agent: synthesis, biodistribution, and microPET imaging.N-benzylisatin sulfonamide analogues as potent caspase-3 inhibitors: synthesis, in vitro activity, and molecular modeling studies.Microfluidic Preparation of a 89Zr-Labeled Trastuzumab Single-Patient Dose.Molecular modeling of hexakis(areneisonitrile)technetium(I), tricarbonyl eta5 cyclopentadienyl technetium and technetium(V)-oxo complexes: MM3 parameter development and prediction of biological properties.Multiple functional neurosteroid binding sites on GABAA receptorsAssessment of Copper Nanoclusters for Accurate in Vivo Tumor Imaging and Potential for TranslationThe molecular determinants of neurosteroid binding in the GABA(A) receptor
P50
Q28817259-06AB13A4-9D35-4F7B-86FD-E1CC69914524Q34206541-A757D7A8-68E2-423E-9451-C4DF09FDF399Q34785369-7DB0BD4A-AB57-472D-9283-454A84869380Q34972459-0800AB61-4BF6-410D-9516-68A10C6E8721Q35565660-4625A311-3986-4A86-9DCE-1FAF80FB3B73Q35748598-5E61A6D3-1A02-4FA0-B82F-454814C9BF05Q36446048-247F2010-3B47-45DE-92B2-CB58A27AF31AQ36479708-744661F7-DF2C-4326-9BE1-6F3FD84E31ECQ36934661-EFDA5B5D-B4E1-4FC7-9B7A-01D4BF6E165CQ37070133-0A243C17-0CB2-4B70-A89B-B107AC1D1F42Q37240859-EBEFE406-0D26-40FE-B385-CFA2B86FC0EDQ37714259-86554106-7D99-4380-9581-38DB92FA5949Q38552997-45D1487B-4649-47B5-96F4-1BE6FE9439BAQ38770769-AEF569F6-E066-4033-AEE4-0CF8BA33A42EQ40159996-D5116998-43C2-420B-882B-FAB624CC5E29Q40479512-99F08EF2-2093-41DD-8B9B-0E238E1AFE57Q41629621-4E3B3474-981A-4FE5-A080-48AD42EE423EQ42860837-0317F1F0-04B5-441F-A986-71084B4E3E1EQ43739036-D823E472-6401-4A58-94A6-89EAE4DF8E62Q44277107-64FE97EE-4691-4B8A-8361-72E9EA744BDCQ44409115-2647F932-2FDB-4B45-A948-EFFE63E0FC40Q44589883-A9A3EFDC-9719-4624-9E0B-A97EEFB023B9Q45031847-76018152-EC5C-45DC-B9F9-B0AABC8338E2Q45179947-7B392C0F-FB3B-4CAE-878C-1E06315CE47AQ46556836-0D142CE2-9B23-4DE5-898E-C552C10E47C9Q46815927-C917492F-E189-4B47-9066-A574C8C94064Q51471788-25B519F5-0118-4032-9E19-0974BA68C5D4Q51940010-C8D1688F-969E-43D3-95E1-83D8FECCF736Q64123067-F05ABFD9-43F8-4EC7-9DE4-AE6722831FC3Q91909660-5DEA46E2-7F77-4436-919D-C207F3BCBEE6Q92443365-CCADB2F0-A1F4-497F-9BE8-24A80807227C
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
David E Reichert
@ast
David E Reichert
@en
David E Reichert
@es
David E Reichert
@nl
David E Reichert
@sl
type
label
David E Reichert
@ast
David E Reichert
@en
David E Reichert
@es
David E Reichert
@nl
David E Reichert
@sl
prefLabel
David E Reichert
@ast
David E Reichert
@en
David E Reichert
@es
David E Reichert
@nl
David E Reichert
@sl
P1053
B-3281-2009
P106
P21
P31
P3829
P496
0000-0003-3432-8998