Lindeberg G - Search Results

1

In vitro and in vivo evaluation of a (18)F-labeled high affinity NOTA conjugated bombesin antagonist as a PET ligand for GRPR-targeted tumor imaging.

Varasteh Z, Aberg O, Velikyan I, Lindeberg G, Sörensen J, Larhed M, Antoni G, Sandström M, Tolmachev V, Orlova A. Varasteh Z, et al. Among authors: lindeberg g. PLoS One. 2013 Dec 3;8(12):e81932. doi: 10.1371/journal.pone.0081932. eCollection 2013. PLoS One. 2013. PMID: 24312607 Free PMC article.

2

Synthesis and characterization of a high-affinity NOTA-conjugated bombesin antagonist for GRPR-targeted tumor imaging.

Varasteh Z, Velikyan I, Lindeberg G, Sörensen J, Larhed M, Sandström M, Selvaraju RK, Malmberg J, Tolmachev V, Orlova A. Varasteh Z, et al. Among authors: lindeberg g. Bioconjug Chem. 2013 Jul 17;24(7):1144-53. doi: 10.1021/bc300659k. Epub 2013 Jul 2. Bioconjug Chem. 2013. PMID: 23763444

3

The effect of mini-PEG-based spacer length on binding and pharmacokinetic properties of a 68Ga-labeled NOTA-conjugated antagonistic analog of bombesin.

Varasteh Z, Rosenström U, Velikyan I, Mitran B, Altai M, Honarvar H, Rosestedt M, Lindeberg G, Sörensen J, Larhed M, Tolmachev V, Orlova A. Varasteh Z, et al. Among authors: lindeberg g. Molecules. 2014 Jul 17;19(7):10455-72. doi: 10.3390/molecules190710455. Molecules. 2014. PMID: 25036155 Free PMC article.

4

The effect of macrocyclic chelators on the targeting properties of the 68Ga-labeled gastrin releasing peptide receptor antagonist PEG2-RM26.

Varasteh Z, Mitran B, Rosenström U, Velikyan I, Rosestedt M, Lindeberg G, Sörensen J, Larhed M, Tolmachev V, Orlova A. Varasteh Z, et al. Among authors: lindeberg g. Nucl Med Biol. 2015 May;42(5):446-454. doi: 10.1016/j.nucmedbio.2014.12.009. Epub 2014 Dec 20. Nucl Med Biol. 2015. PMID: 25684649

5

Selection of optimal chelator improves the contrast of GRPR imaging using bombesin analogue RM26.

Mitran B, Varasteh Z, Selvaraju RK, Lindeberg G, Sörensen J, Larhed M, Tolmachev V, Rosenström U, Orlova A. Mitran B, et al. Among authors: lindeberg g. Int J Oncol. 2016 May;48(5):2124-34. doi: 10.3892/ijo.2016.3429. Epub 2016 Mar 9. Int J Oncol. 2016. PMID: 26983776

6

Angiotensin II pseudopeptides containing 1,3,5-trisubstituted benzene scaffolds with high AT2 receptor affinity.

Georgsson J, Sköld C, Plouffe B, Lindeberg G, Botros M, Larhed M, Nyberg F, Gallo-Payet N, Gogoll A, Karlén A, Hallberg A. Georgsson J, et al. Among authors: lindeberg g. J Med Chem. 2005 Oct 20;48(21):6620-31. doi: 10.1021/jm050280z. J Med Chem. 2005. PMID: 16220978

7

Synthesis of a new class of druglike angiotensin II C-terminal mimics with affinity for the AT2 receptor.

Georgsson J, Sköld C, Botros M, Lindeberg G, Nyberg F, Karlén A, Hallberg A, Larhed M. Georgsson J, et al. Among authors: lindeberg g. J Med Chem. 2007 Apr 5;50(7):1711-5. doi: 10.1021/jm0613469. Epub 2007 Mar 15. J Med Chem. 2007. PMID: 17358051

8

Discovery of dipeptides with high affinity to the specific binding site for substance P1-7.

Fransson R, Botros M, Sköld C, Nyberg F, Lindeberg G, Hallberg M, Sandström A. Fransson R, et al. Among authors: lindeberg g. J Med Chem. 2010 Mar 25;53(6):2383-9. doi: 10.1021/jm901352b. J Med Chem. 2010. PMID: 20178322

9

Ligands to the (IRAP)/AT4 receptor encompassing a 4-hydroxydiphenylmethane scaffold replacing Tyr2.

Andersson H, Demaegdt H, Vauquelin G, Lindeberg G, Karlén A, Hallberg M. Andersson H, et al. Among authors: lindeberg g. Bioorg Med Chem. 2008 Jul 15;16(14):6924-35. doi: 10.1016/j.bmc.2008.05.046. Epub 2008 May 27. Bioorg Med Chem. 2008. PMID: 18556208

10

New selective AT2 receptor ligands encompassing a gamma-turn mimetic replacing the amino acid residues 4-5 of angiotensin II act as agonists.

Rosenström U, Sköld C, Plouffe B, Beaudry H, Lindeberg G, Botros M, Nyberg F, Wolf G, Karlén A, Gallo-Payet N, Hallberg A. Rosenström U, et al. Among authors: lindeberg g. J Med Chem. 2005 Jun 16;48(12):4009-24. doi: 10.1021/jm0491492. J Med Chem. 2005. PMID: 15943474

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