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Bioorganic & Medicinal Chemistry
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November 14, 2008
Structure-activity relationship studies of a new series of imidazo[2,1-f]purinones as potent and selective A(3) adenosine receptor antagonists
Pier Giovanni Baraldi, Delia Preti, Mojgan Aghazadeh Tabrizi, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 12, 2005
Synthesis and preliminary biological evaluation of new anti-tubulin agents containing different benzoheterocycles
Romeo Romagnoli, Pier Giovanni Baraldi, M Katherine Jung, et al.
Journal of Medicinal Chemistry
|
August 12, 2009
2-Arylamino-4-amino-5-aroylthiazoles. "One-pot" synthesis and biological evaluation of a new class of inhibitors of tubulin polymerization
Romeo Romagnoli, Pier Giovanni Baraldi, Maria Dora Carrion, et al.
Journal of Medicinal Chemistry
|
May 24, 2013
Discovery of 7-oxopyrazolo[1,5-a]pyrimidine-6-carboxamides as potent and selective CB(2) cannabinoid receptor inverse agonists
Mojgan Aghazadeh Tabrizi, Pier Giovanni Baraldi, Giulia Saponaro, et al.
Medicinal Research Reviews
|
July 7, 2017
A<sub>3</sub> Adenosine Receptors as Modulators of Inflammation: From Medicinal Chemistry to Therapy
Kenneth A Jacobson, Stefania Merighi, Katia Varani, et al.
Journal of Medicinal Chemistry
|
December 14, 2011
Novel 1,3-dipropyl-8-(3-benzimidazol-2-yl-methoxy-1-methylpyrazol-5-yl)xanthines as potent and selective A₂B adenosine receptor antagonists
Pier Giovanni Baraldi, Stefania Baraldi, Giulia Saponaro, et al.
European Journal of Medicinal Chemistry
|
October 27, 2011
One-pot synthesis and biological evaluation of 2-pyrrolidinyl-4-amino-5-(3',4',5'-trimethoxybenzoyl)thiazole: a unique, highly active antimicrotubule agent
Romeo Romagnoli, Pier Giovanni Baraldi, Carlota Lopez Cara, et al.
Journal of Medicinal Chemistry
|
December 6, 2011
Synthesis and evaluation of 1,5-disubstituted tetrazoles as rigid analogues of combretastatin A-4 with potent antiproliferative and antitumor activity
Romeo Romagnoli, Pier Giovanni Baraldi, Maria Kimatrai Salvador, et al.
Journal of Medicinal Chemistry
|
June 26, 2007
From tyrosine to glycine: synthesis and biological activity of potent antagonists of the purinergic P2X7 receptor
Romeo Romagnoli, Pier Giovanni Baraldi, Maria Dora Carrion, et al.
Journal of Medicinal Chemistry
|
August 30, 2008
Synthesis and biological evaluation of 2-amino-3-(4-chlorobenzoyl)-4-[N-(substituted) piperazin-1-yl]thiophenes as potent allosteric enhancers of the A1 adenosine receptor
Romeo Romagnoli, Pier Giovanni Baraldi, Maria Dora Carrion, et al.
Page
of 16
Search research articles
Search
Showing results (121-130 of 159) with videos related to
Sort By:
Page
of 16
Bioorganic & Medicinal Chemistry
|
November 14, 2008
Structure-activity relationship studies of a new series of imidazo[2,1-f]purinones as potent and selective A(3) adenosine receptor antagonists
Pier Giovanni Baraldi, Delia Preti, Mojgan Aghazadeh Tabrizi, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 12, 2005
Synthesis and preliminary biological evaluation of new anti-tubulin agents containing different benzoheterocycles
Romeo Romagnoli, Pier Giovanni Baraldi, M Katherine Jung, et al.
Journal of Medicinal Chemistry
|
August 12, 2009
2-Arylamino-4-amino-5-aroylthiazoles. "One-pot" synthesis and biological evaluation of a new class of inhibitors of tubulin polymerization
Romeo Romagnoli, Pier Giovanni Baraldi, Maria Dora Carrion, et al.
Journal of Medicinal Chemistry
|
May 24, 2013
Discovery of 7-oxopyrazolo[1,5-a]pyrimidine-6-carboxamides as potent and selective CB(2) cannabinoid receptor inverse agonists
Mojgan Aghazadeh Tabrizi, Pier Giovanni Baraldi, Giulia Saponaro, et al.
Medicinal Research Reviews
|
July 7, 2017
A<sub>3</sub> Adenosine Receptors as Modulators of Inflammation: From Medicinal Chemistry to Therapy
Kenneth A Jacobson, Stefania Merighi, Katia Varani, et al.
Journal of Medicinal Chemistry
|
December 14, 2011
Novel 1,3-dipropyl-8-(3-benzimidazol-2-yl-methoxy-1-methylpyrazol-5-yl)xanthines as potent and selective A₂B adenosine receptor antagonists
Pier Giovanni Baraldi, Stefania Baraldi, Giulia Saponaro, et al.
European Journal of Medicinal Chemistry
|
October 27, 2011
One-pot synthesis and biological evaluation of 2-pyrrolidinyl-4-amino-5-(3',4',5'-trimethoxybenzoyl)thiazole: a unique, highly active antimicrotubule agent
Romeo Romagnoli, Pier Giovanni Baraldi, Carlota Lopez Cara, et al.
Journal of Medicinal Chemistry
|
December 6, 2011
Synthesis and evaluation of 1,5-disubstituted tetrazoles as rigid analogues of combretastatin A-4 with potent antiproliferative and antitumor activity
Romeo Romagnoli, Pier Giovanni Baraldi, Maria Kimatrai Salvador, et al.
Journal of Medicinal Chemistry
|
June 26, 2007
From tyrosine to glycine: synthesis and biological activity of potent antagonists of the purinergic P2X7 receptor
Romeo Romagnoli, Pier Giovanni Baraldi, Maria Dora Carrion, et al.
Journal of Medicinal Chemistry
|
August 30, 2008
Synthesis and biological evaluation of 2-amino-3-(4-chlorobenzoyl)-4-[N-(substituted) piperazin-1-yl]thiophenes as potent allosteric enhancers of the A1 adenosine receptor
Romeo Romagnoli, Pier Giovanni Baraldi, Maria Dora Carrion, et al.
Page
of 16