Camaioni E - Search Results

1

Targeting Wnt-driven cancers: Discovery of novel tankyrase inhibitors.

Ferri M, Liscio P, Carotti A, Asciutti S, Sardella R, Macchiarulo A, Camaioni E. Ferri M, et al. Among authors: camaioni e. Eur J Med Chem. 2017 Dec 15;142:506-522. doi: 10.1016/j.ejmech.2017.09.030. Epub 2017 Oct 7. Eur J Med Chem. 2017. PMID: 29107427 Review.

2

Metabotropic glutamate receptors: structure and new subtype-selective ligands.

Pellicciari R, Costantino G, Marinozzi M, Macchiarulo A, Camaioni E, Natalini B. Pellicciari R, et al. Among authors: camaioni e. Farmaco. 2001 Jan-Feb;56(1-2):91-4. doi: 10.1016/s0014-827x(01)01006-0. Farmaco. 2001. PMID: 11347974 Review.

3

Modeling of poly(ADP-ribose)polymerase (PARP) inhibitors. Docking of ligands and quantitative structure-activity relationship analysis.

Costantino G, Macchiarulo A, Camaioni E, Pellicciari R. Costantino G, et al. Among authors: camaioni e. J Med Chem. 2001 Nov 8;44(23):3786-94. doi: 10.1021/jm010116l. J Med Chem. 2001. PMID: 11689065

4

Spiro[2.2]pentane as a dissymmetric scaffold for conformationally constrained analogues of glutamic acid: focus on racemic 1-aminospiro[2.2]pentyl-1,4-dicarboxylic acids.

Pellicciari R, Marinozzi M, Camaioni E, del Carmen Nùnez M, Costantino G, Gasparini F, Giorgi G, Macchiarulo A, Subramanian N. Pellicciari R, et al. Among authors: camaioni e. J Org Chem. 2002 Aug 9;67(16):5497-507. doi: 10.1021/jo020138v. J Org Chem. 2002. PMID: 12153247

5

Binding mode of 6ECDCA, a potent bile acid agonist of the farnesoid X receptor (FXR).

Costantino G, Macchiarulo A, Entrena-Guadix A, Camaioni E, Pellicciari R. Costantino G, et al. Among authors: camaioni e. Bioorg Med Chem Lett. 2003 Jun 2;13(11):1865-8. doi: 10.1016/s0960-894x(03)00281-6. Bioorg Med Chem Lett. 2003. PMID: 12749886

6

Towards new neuroprotective agents: design and synthesis of 4H-thieno[2,3-c] isoquinolin-5-one derivatives as potent PARP-1 inhibitors.

Pellicciari R, Camaioni E, Costantino G, Marinozzi M, Macchiarulo A, Moroni F, Natalini B. Pellicciari R, et al. Among authors: camaioni e. Farmaco. 2003 Sep;58(9):851-8. doi: 10.1016/S0014-827X(03)00143-5. Farmaco. 2003. PMID: 13679179

7

Rat brain guanosine binding site. Biological studies and pseudo-receptor construction.

Traversa U, Bombi G, Camaioni E, Macchiarulo A, Costantino G, Palmieri C, Caciagli F, Pellicciari R. Traversa U, et al. Among authors: camaioni e. Bioorg Med Chem. 2003 Dec 1;11(24):5417-25. doi: 10.1016/j.bmc.2003.09.043. Bioorg Med Chem. 2003. PMID: 14642586

8

3alpha-6alpha-Dihydroxy-7alpha-fluoro-5beta-cholanoate (UPF-680), physicochemical and physiological properties of a new fluorinated bile acid that prevents 17alpha-ethynyl-estradiol-induced cholestasis in rats.

Clerici C, Castellani D, Asciutti S, Pellicciari R, Setchell KD, O'Connell NC, Sadeghpour B, Camaioni E, Fiorucci S, Renga B, Nardi E, Sabatino G, Clementi M, Giuliano V, Baldoni M, Orlandi S, Mazzocchi A, Morelli A, Morelli O. Clerici C, et al. Among authors: camaioni e. Toxicol Appl Pharmacol. 2006 Jul 15;214(2):199-208. doi: 10.1016/j.taap.2005.12.017. Epub 2006 Feb 17. Toxicol Appl Pharmacol. 2006. PMID: 16487557

9

Correlation between CMC and chromatographic index: simple and effective evaluation of the hydrophobic/hydrophilic balance of bile acids.

Natalini B, Sardella R, Camaioni E, Gioiello A, Pellicciari R. Natalini B, et al. Among authors: camaioni e. Anal Bioanal Chem. 2007 Aug;388(8):1681-8. doi: 10.1007/s00216-007-1360-6. Epub 2007 Jun 16. Anal Bioanal Chem. 2007. PMID: 17572887

10

Molecular docking and spatial coarse graining simulations as tools to investigate substrate recognition, enhancer binding and conformational transitions in indoleamine-2,3-dioxygenase (IDO).

Macchiarulo A, Nuti R, Bellocchi D, Camaioni E, Pellicciari R. Macchiarulo A, et al. Among authors: camaioni e. Biochim Biophys Acta. 2007 Aug;1774(8):1058-68. doi: 10.1016/j.bbapap.2007.06.007. Epub 2007 Jul 6. Biochim Biophys Acta. 2007. PMID: 17644054

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