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Andrea Spallarossa

Showing results (51-60 of 68) with videos related to

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European Journal of Medicinal Chemistry|August 1, 2008
N-acylated and N,N'-diacylated imidazolidine-2-thione derivatives and N,N'-diacylated tetrahydropyrimidine-2(1H)-thione analogues: synthesis and antiproliferative activitySara Cesarini, Andrea Spallarossa, Angelo Ranise, et al.
Bioorganic & Medicinal Chemistry|April 28, 2009
6-amino-4-oxo-1,3-diphenyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonyl derivatives as a new class of potent inhibitors of Interleukin-8-induced neutrophil chemotaxisSara Cesarini, Andrea Spallarossa, Angelo Ranise, et al.
Biochemical and Biophysical Research Communications|September 3, 2003
Structure of the human NK cell triggering receptor NKp46 ectodomainMarco Ponassi, Claudia Cantoni, Roberto Biassoni, et al.
Bioorganic & Medicinal Chemistry|September 26, 2013
Further SAR studies on bicyclic basic merbarone analogues as potent antiproliferative agentsAndrea Spallarossa, Chiara Rotolo, Claudia Sissi, et al.
Bioorganic & Medicinal Chemistry|May 27, 2008
Parallel one-pot synthesis and structure-activity relationship study of symmetric formimidoester disulfides as a novel class of potent non-nucleoside HIV-1 reverse transcriptase inhibitorsSara Cesarini, Andrea Spallarossa, Angelo Ranise, et al.
European Journal of Medicinal Chemistry|October 29, 2008
Novel modifications in the series of O-(2-phthalimidoethyl)-N-substituted thiocarbamates and their ring-opened congeners as non-nucleoside HIV-1 reverse transcriptase inhibitorsAndrea Spallarossa, Sara Cesarini, Angelo Ranise, et al.
Chemmedchem|June 24, 2025
Targeting Ubiquitin-Specific Protease 7 with Novel 5-Amino-Pyrazole Inhibitors: Design, Synthesis, and Biological EvaluationMatteo Lusardi, Elva Morretta, Andrea Spallarossa, et al.
Journal of Medicinal Chemistry|February 21, 2003
Design, synthesis, SAR, and molecular modeling studies of acylthiocarbamates: a novel series of potent non-nucleoside HIV-1 reverse transcriptase inhibitors structurally related to phenethylthiazolylthiourea derivativesAngelo Ranise, Andrea Spallarossa, Silvia Schenone, et al.
Bioorganic & Medicinal Chemistry|May 22, 2003
Synthesis and antiproliferative activity of basic thioanalogues of merbaroneAngelo Ranise, Andrea Spallarossa, Silvia Schenone, et al.
Molecules (Basel, Switzerland)|May 25, 2024
Investigations of Antioxidant and Anti-Cancer Activities of 5-Aminopyrazole DerivativesFederica Rapetti, Andrea Spallarossa, Eleonora Russo, et al.
Pageof 7

Showing results (51-60 of 68) with videos related to

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Pageof 7
European Journal of Medicinal Chemistry|August 1, 2008
N-acylated and N,N'-diacylated imidazolidine-2-thione derivatives and N,N'-diacylated tetrahydropyrimidine-2(1H)-thione analogues: synthesis and antiproliferative activitySara Cesarini, Andrea Spallarossa, Angelo Ranise, et al.
Bioorganic & Medicinal Chemistry|April 28, 2009
6-amino-4-oxo-1,3-diphenyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonyl derivatives as a new class of potent inhibitors of Interleukin-8-induced neutrophil chemotaxisSara Cesarini, Andrea Spallarossa, Angelo Ranise, et al.
Biochemical and Biophysical Research Communications|September 3, 2003
Structure of the human NK cell triggering receptor NKp46 ectodomainMarco Ponassi, Claudia Cantoni, Roberto Biassoni, et al.
Bioorganic & Medicinal Chemistry|September 26, 2013
Further SAR studies on bicyclic basic merbarone analogues as potent antiproliferative agentsAndrea Spallarossa, Chiara Rotolo, Claudia Sissi, et al.
Bioorganic & Medicinal Chemistry|May 27, 2008
Parallel one-pot synthesis and structure-activity relationship study of symmetric formimidoester disulfides as a novel class of potent non-nucleoside HIV-1 reverse transcriptase inhibitorsSara Cesarini, Andrea Spallarossa, Angelo Ranise, et al.
European Journal of Medicinal Chemistry|October 29, 2008
Novel modifications in the series of O-(2-phthalimidoethyl)-N-substituted thiocarbamates and their ring-opened congeners as non-nucleoside HIV-1 reverse transcriptase inhibitorsAndrea Spallarossa, Sara Cesarini, Angelo Ranise, et al.
Chemmedchem|June 24, 2025
Targeting Ubiquitin-Specific Protease 7 with Novel 5-Amino-Pyrazole Inhibitors: Design, Synthesis, and Biological EvaluationMatteo Lusardi, Elva Morretta, Andrea Spallarossa, et al.
Journal of Medicinal Chemistry|February 21, 2003
Design, synthesis, SAR, and molecular modeling studies of acylthiocarbamates: a novel series of potent non-nucleoside HIV-1 reverse transcriptase inhibitors structurally related to phenethylthiazolylthiourea derivativesAngelo Ranise, Andrea Spallarossa, Silvia Schenone, et al.
Bioorganic & Medicinal Chemistry|May 22, 2003
Synthesis and antiproliferative activity of basic thioanalogues of merbaroneAngelo Ranise, Andrea Spallarossa, Silvia Schenone, et al.
Molecules (Basel, Switzerland)|May 25, 2024
Investigations of Antioxidant and Anti-Cancer Activities of 5-Aminopyrazole DerivativesFederica Rapetti, Andrea Spallarossa, Eleonora Russo, et al.
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