Lodola A - Search Results

1

Dual mechanisms of action of the 5-benzylidene-hydantoin UPR1024 on lung cancer cell lines.

Cavazzoni A, Alfieri RR, Carmi C, Zuliani V, Galetti M, Fumarola C, Frazzi R, Bonelli M, Bordi F, Lodola A, Mor M, Petronini PG. Cavazzoni A, et al. Among authors: lodola a. Mol Cancer Ther. 2008 Feb;7(2):361-70. doi: 10.1158/1535-7163.MCT-07-0477. Mol Cancer Ther. 2008. PMID: 18281519

2

Synthesis, pharmacological evaluation, and structure-activity relationships of benzopyran derivatives with potent SERM activity.

Amari G, Armani E, Ghirardi S, Delcanale M, Civelli M, Caruso PL, Galbiati E, Lipreri M, Rivara S, Lodola A, Mor M. Amari G, et al. Among authors: lodola a. Bioorg Med Chem. 2004 Jul 15;12(14):3763-82. doi: 10.1016/j.bmc.2004.05.015. Bioorg Med Chem. 2004. PMID: 15210143

3

Cyclohexylcarbamic acid 3'- or 4'-substituted biphenyl-3-yl esters as fatty acid amide hydrolase inhibitors: synthesis, quantitative structure-activity relationships, and molecular modeling studies.

Mor M, Rivara S, Lodola A, Plazzi PV, Tarzia G, Duranti A, Tontini A, Piersanti G, Kathuria S, Piomelli D. Mor M, et al. Among authors: lodola a. J Med Chem. 2004 Oct 7;47(21):4998-5008. doi: 10.1021/jm031140x. J Med Chem. 2004. PMID: 15456244 Free article.

4

QM/MM modelling of oleamide hydrolysis in fatty acid amide hydrolase (FAAH) reveals a new mechanism of nucleophile activation.

Lodola A, Mor M, Hermann JC, Tarzia G, Piomelli D, Mulholland AJ. Lodola A, et al. Chem Commun (Camb). 2005 Sep 21;(35):4399-401. doi: 10.1039/b503887a. Epub 2005 Jul 11. Chem Commun (Camb). 2005. PMID: 16136230 Free article.

5

5-benzylidene-hydantoins as new EGFR inhibitors with antiproliferative activity.

Carmi C, Cavazzoni A, Zuliani V, Lodola A, Bordi F, Plazzi PV, Alfieri RR, Petronini PG, Mor M. Carmi C, et al. Among authors: lodola a. Bioorg Med Chem Lett. 2006 Aug 1;16(15):4021-5. doi: 10.1016/j.bmcl.2006.05.010. Epub 2006 May 19. Bioorg Med Chem Lett. 2006. PMID: 16713265

6

Synthesis and structure-activity relationships of FAAH inhibitors: cyclohexylcarbamic acid biphenyl esters with chemical modulation at the proximal phenyl ring.

Tarzia G, Duranti A, Gatti G, Piersanti G, Tontini A, Rivara S, Lodola A, Plazzi PV, Mor M, Kathuria S, Piomelli D. Tarzia G, et al. Among authors: lodola a. ChemMedChem. 2006 Jan;1(1):130-9. doi: 10.1002/cmdc.200500017. ChemMedChem. 2006. PMID: 16892344

7

Application of 3D-QSAR in the rational design of receptor ligands and enzyme inhibitors.

Mor M, Rivara S, Lodola A, Lorenzi S, Bordi F, Plazzi PV, Spadoni G, Bedini A, Duranti A, Tontini A, Tarzia G. Mor M, et al. Among authors: lodola a. Chem Biodivers. 2005 Nov;2(11):1438-51. doi: 10.1002/cbdv.200590117. Chem Biodivers. 2005. PMID: 17191945

8

Synthesis, enantiomeric resolution, and structure-activity relationship study of a series of 10,11-dihydro-5H-dibenzo[a,d]cycloheptene MT2 receptor antagonists.

Spadoni G, Bedini A, Diamantini G, Tarzia G, Rivara S, Lorenzi S, Lodola A, Mor M, Lucini V, Pannacci M, Caronno A, Fraschini F. Spadoni G, et al. Among authors: lodola a. ChemMedChem. 2007 Dec;2(12):1741-9. doi: 10.1002/cmdc.200700141. ChemMedChem. 2007. PMID: 17907131

9

N-(substituted-anilinoethyl)amides: design, synthesis, and pharmacological characterization of a new class of melatonin receptor ligands.

Rivara S, Lodola A, Mor M, Bedini A, Spadoni G, Lucini V, Pannacci M, Fraschini F, Scaglione F, Sanchez RO, Gobbi G, Tarzia G. Rivara S, et al. Among authors: lodola a. J Med Chem. 2007 Dec 27;50(26):6618-26. doi: 10.1021/jm700957j. Epub 2007 Dec 6. J Med Chem. 2007. PMID: 18052314

10

Identification of productive inhibitor binding orientation in fatty acid amide hydrolase (FAAH) by QM/MM mechanistic modelling.

Lodola A, Mor M, Rivara S, Christov C, Tarzia G, Piomelli D, Mulholland AJ. Lodola A, et al. Chem Commun (Camb). 2008 Jan 14;(2):214-6. doi: 10.1039/b714136j. Epub 2007 Oct 19. Chem Commun (Camb). 2008. PMID: 18092091

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