Lolli ML - Search Results

1

New aldo-keto reductase 1C3 (AKR1C3) inhibitors based on the hydroxytriazole scaffold.

Pippione AC, Kilic-Kurt Z, Kovachka S, Sainas S, Rolando B, Denasio E, Pors K, Adinolfi S, Zonari D, Bagnati R, Lolli ML, Spyrakis F, Oliaro-Bosso S, Boschi D. Pippione AC, et al. Among authors: lolli ml. Eur J Med Chem. 2022 Jul 5;237:114366. doi: 10.1016/j.ejmech.2022.114366. Epub 2022 Apr 13. Eur J Med Chem. 2022. PMID: 35447434 Free article.

2

Urinary excretion of O6-butylguanine after the administration of N-nitroso-N-butylurea in rats.

Airoldi L, Galli A, Magagnotti C, Bagnati R, Lolli M, Fanelli R. Airoldi L, et al. Cancer Res. 1992 Dec 1;52(23):6699-701. Cancer Res. 1992. PMID: 1423317

3

Synthesis of NO-donor bisphosphonates and their in-vitro action on bone resorption.

Lazzarato L, Rolando B, Lolli ML, Tron GC, Fruttero R, Gasco A, Deleide G, Guenther HL. Lazzarato L, et al. Among authors: lolli ml. J Med Chem. 2005 Mar 10;48(5):1322-9. doi: 10.1021/jm040830d. J Med Chem. 2005. PMID: 15743175

4

Hydroxy-1,2,5-oxadiazolyl moiety as bioisoster of the carboxy function. Synthesis, ionization constants, and pharmacological characterization of gamma-aminobutyric acid (GABA) related compounds.

Lolli ML, Hansen SL, Rolando B, Nielsen B, Wellendorph P, Madsen K, Larsen OM, Kristiansen U, Fruttero R, Gasco A, Johansen TN. Lolli ML, et al. J Med Chem. 2006 Jul 13;49(14):4442-6. doi: 10.1021/jm051288b. J Med Chem. 2006. PMID: 16821803

5

Synthesis and preliminary pharmacological characterisation of a new class of nitrogen-containing bisphosphonates (N-BPs).

Lolli ML, Rolando B, Tosco P, Chaurasia S, Di Stilo A, Lazzarato L, Gorassini E, Ferracini R, Oliaro-Bosso S, Fruttero R, Gasco A. Lolli ML, et al. Bioorg Med Chem. 2010 Apr 1;18(7):2428-38. doi: 10.1016/j.bmc.2010.02.058. Epub 2010 Mar 1. Bioorg Med Chem. 2010. PMID: 20299227 Free article.

6

4-hydroxy-1,2,5-oxadiazol-3-yl moiety as bioisoster of the carboxy function. Synthesis, ionization constants, and molecular pharmacological characterization at ionotropic glutamate receptors of compounds related to glutamate and its homologues.

Lolli ML, Giordano C, Pickering DS, Rolando B, Hansen KB, Foti A, Contreras-Sanz A, Amir A, Fruttero R, Gasco A, Nielsen B, Johansen TN. Lolli ML, et al. J Med Chem. 2010 May 27;53(10):4110-8. doi: 10.1021/jm1001452. J Med Chem. 2010. PMID: 20408529 Free article.

7

1,2,5-Oxadiazole analogues of leflunomide and related compounds.

Giorgis M, Lolli ML, Rolando B, Rao A, Tosco P, Chaurasia S, Marabello D, Fruttero R, Gasco A. Giorgis M, et al. Among authors: lolli ml. Eur J Med Chem. 2011 Jan;46(1):383-92. doi: 10.1016/j.ejmech.2010.10.029. Epub 2010 Nov 3. Eur J Med Chem. 2011. PMID: 21109332

8

Searching for new NO-donor aspirin-like molecules: Furoxanylacyl derivatives of salicylic acid and related furazans.

Lazzarato L, Cena C, Rolando B, Marini E, Lolli ML, Guglielmo S, Guaita E, Morini G, Coruzzi G, Fruttero R, Gasco A. Lazzarato L, et al. Among authors: lolli ml. Bioorg Med Chem. 2011 Oct 1;19(19):5852-60. doi: 10.1016/j.bmc.2011.08.018. Epub 2011 Aug 16. Bioorg Med Chem. 2011. PMID: 21906954

9

Refining the chemical toolbox to be fit for educational and practical purpose for drug discovery in the 21st Century.

Lolli M, Narramore S, Fishwick CW, Pors K. Lolli M, et al. Drug Discov Today. 2015 Aug;20(8):1018-26. doi: 10.1016/j.drudis.2015.04.010. Epub 2015 May 7. Drug Discov Today. 2015. PMID: 25959506 Free article. Review.

10

Heterocyclic ring cleavage upon collision-induced dissociation of deprotonated 3-hydroxy-1,2,5-oxadiazoles (3-hydroxyfurazans).

Grossert JS, Pippione AC, Boschi D, Lolli ML, White RL. Grossert JS, et al. Among authors: lolli ml. J Mass Spectrom. 2015 Dec;50(12):1433-7. doi: 10.1002/jms.3724. J Mass Spectrom. 2015. PMID: 26634978

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