Literature DB >> 16741315

Synthesis and in vivo evaluation of 2 high-affinity 76Br-labeled sigma2-receptor ligands.

Douglas J Rowland1, Zhude Tu, Jinbin Xu, Datta Ponde, Robert H Mach, Michael J Welch.   

Abstract

UNLABELLED: The sigma(2)-receptor has been shown to be upregulated in proliferating tumors cells. The purpose of this study was to compare 3'-deoxy-3'-(18)F-fluorothymidine ((18)F-FLT) and 2 new (76)Br-radiolabeled compounds that have a high affinity and selectivity for the sigma(2)-receptor. These are 5-bromo-N-(4-(3,4-dihydro-6,7-dimethoxyisoquinolin-2(1H)-yl)butyl)-2,3-dimethoxybenzamide (compound (1)) and 5-bromo-N-(2-(3,4-dihydro-6,7-dimethoxyisoquinolin-2(1H)-yl)ethyl)-2-methoxybenzamide (compound (2)).
METHODS: Two sigma(2)-receptor-binding ligands were prepared, from the corresponding tributylstannyl precursors using standard electrophilic chemistry, (76)Br-compound (1) ((76)Br-1) and (76)Br-compound (2) ((76)Br-2). (18)F-FLT, (76)Br-1, and (76)Br-2 were compared using allograft tumors of the EMT-6 cell line (mouse mammary adenocarcinoma) in biodistribution studies at 5 min, 0.5, 1, and 2 h. Imaging of (76)Br-1 and (18)F-FLT was also performed at 2 and 1 h, respectively.
RESULTS: (76)Br-1 and (76)Br-2 were synthesized with yields between 50% and 70% with high specific activity. Both compounds showed uptake into the tumor with tumor-to-normal tissue ratios of (76)Br-1 being greater than both (76)Br-2 and (18)F-FLT. Except for the liver and kidney, all ratios were greater than 1 and uptake into the tumor was shown with microPET imaging for (76)Br-1.
CONCLUSION: We were able to synthesize two (76)Br-radiolabeled compounds with a high yield and specific activity that target the sigma(2) receptor with high affinity and selectivity. The studies presented show that both of the flexible benzamide compounds can identify EMT-6 breast tumors in vivo. (76)Br-1 also has higher tumor-to-normal tissue ratios when compared with (76)Br-2 and (18)F-FLT. The high affinity and low nonspecific binding of (76)Br-1 indicates that it can be a potential PET radiotracer for imaging solid tumors.

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Year:  2006        PMID: 16741315

Source DB:  PubMed          Journal:  J Nucl Med        ISSN: 0161-5505            Impact factor:   10.057


  13 in total

1.  Synthesis and in vitro evaluation of tetrahydroisoquinolinyl benzamides as ligands for sigma receptors.

Authors:  Rong Xu; John R Lever; Susan Z Lever
Journal:  Bioorg Med Chem Lett       Date:  2007-02-04       Impact factor: 2.823

Review 2.  Development of molecular probes for imaging sigma-2 receptors in vitro and in vivo.

Authors:  Robert Henry Mach; Kenneth Theodore Wheeler
Journal:  Cent Nerv Syst Agents Med Chem       Date:  2009-09

3.  Radiosynthesis and biological evaluation of a promising sigma(2)-receptor ligand radiolabeled with fluorine-18 or iodine-125 as a PET/SPECT probe for imaging breast cancer.

Authors:  Zhude Tu; Jinbin Xu; Lynne A Jones; Shihong Li; Dexing Zeng; Mei-Ping Kung; Hank F Kung; Robert H Mach
Journal:  Appl Radiat Isot       Date:  2010-06-15       Impact factor: 1.513

4.  Characterization and evaluation of two novel fluorescent sigma-2 receptor ligands as proliferation probes.

Authors:  Chenbo Zeng; Suwanna Vangveravong; Lynne A Jones; Krzysztof Hyrc; Katherine C Chang; Jinbin Xu; Justin M Rothfuss; Mark P Goldberg; Richard S Hotchkiss; Robert H Mach
Journal:  Mol Imaging       Date:  2011-12       Impact factor: 4.488

5.  Synthesis and pharmacological evaluation of indole-based sigma receptor ligands.

Authors:  Christophe Mésangeau; Emanuele Amata; Walid Alsharif; Michael J Seminerio; Matthew J Robson; Rae R Matsumoto; Jacques H Poupaert; Christopher R McCurdy
Journal:  Eur J Med Chem       Date:  2011-08-29       Impact factor: 6.514

Review 6.  Tactics for preclinical validation of receptor-binding radiotracers.

Authors:  Susan Z Lever; Kuo-Hsien Fan; John R Lever
Journal:  Nucl Med Biol       Date:  2016-09-03       Impact factor: 2.408

Review 7.  The σ2 receptor: a novel protein for the imaging and treatment of cancer.

Authors:  Robert H Mach; Chenbo Zeng; William G Hawkins
Journal:  J Med Chem       Date:  2013-06-18       Impact factor: 7.446

8.  PET Radiotracers for Imaging the Proliferative Status of Solid Tumors.

Authors:  Robert H Mach; Farrokh Dehdashti; Kenneth T Wheeler
Journal:  PET Clin       Date:  2009-01-01

9.  Synthesis and structure-activity relationship studies of conformationally flexible tetrahydroisoquinolinyl triazole carboxamide and triazole substituted benzamide analogues as σ2 receptor ligands.

Authors:  Suping Bai; Shihong Li; Jinbin Xu; Xin Peng; Kiran Sai; Wenhua Chu; Zhude Tu; Chenbo Zeng; Robert H Mach
Journal:  J Med Chem       Date:  2014-05-12       Impact factor: 7.446

10.  Comparative functional evaluation of immunocompetent mouse breast cancer models established from PyMT-tumors using small animal PET with [(18)F]FDG and [(18)F]FLT.

Authors:  Alan Desilva; Melinda Wuest; Monica Wang; Jeff Hummel; Karen Mossman; Frank Wuest; Mary M Hitt
Journal:  Am J Nucl Med Mol Imaging       Date:  2011-12-15
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