Search research articles
Contact Us
Filters
Showing results (21-30 of 39) with videos related to
Page
of 4
Sort By:
Journal of Medicinal Chemistry
|
May 11, 2012
Indole-2-carboxamides as allosteric modulators of the cannabinoid CB₁ receptor
Francesco Piscitelli, Alessia Ligresti, Giuseppe La Regina, et al.
The International Journal of Biochemistry & Cell Biology
|
April 22, 2009
Study of the effects of a new pyrazolecarboxamide: changes in mitochondria and induction of apoptosis
Vincenzo Giansanti, Tania Camboni, Francesco Piscitelli, et al.
Journal of Medicinal Chemistry
|
September 7, 2007
Indolyl aryl sulfones as HIV-1 non-nucleoside reverse transcriptase inhibitors: role of two halogen atoms at the indole ring in developing new analogues with improved antiviral activity
Giuseppe La Regina, Antonio Coluccia, Francesco Piscitelli, et al.
Journal of Medicinal Chemistry
|
March 4, 2011
Indolylarylsulfones as HIV-1 non-nucleoside reverse transcriptase inhibitors: new cyclic substituents at indole-2-carboxamide
Giuseppe La Regina, Antonio Coluccia, Andrea Brancale, et al.
Journal of Medicinal Chemistry
|
February 26, 2008
Synthesis, cannabinoid receptor affinity, and molecular modeling studies of substituted 1-aryl-5-(1H-pyrrol-1-yl)-1H-pyrazole-3-carboxamides
Romano Silvestri, Maria Grazia Cascio, Giuseppe La Regina, et al.
Journal of Medicinal Chemistry
|
April 16, 2010
Discovery of brain-penetrant, orally bioavailable aminothienopyridazine inhibitors of tau aggregation
Carlo Ballatore, Kurt R Brunden, Francesco Piscitelli, et al.
Bioorganic & Medicinal Chemistry
|
June 22, 2012
Aminothienopyridazine inhibitors of tau aggregation: evaluation of structure-activity relationship leads to selection of candidates with desirable in vivo properties
Carlo Ballatore, Alex Crowe, Francesco Piscitelli, et al.
Journal of Medicinal Chemistry
|
August 26, 2011
Cyclopentane-1,3-dione: a novel isostere for the carboxylic acid functional group. Application to the design of potent thromboxane (A2) receptor antagonists
Carlo Ballatore, James H Soper, Francesco Piscitelli, et al.
Journal of Medicinal Chemistry
|
May 26, 2006
Design, molecular modeling, synthesis, and anti-HIV-1 activity of new indolyl aryl sulfones. Novel derivatives of the indole-2-carboxamide
Rino Ragno, Antonio Coluccia, Giuseppe La Regina, et al.
Journal of Medicinal Chemistry
|
June 21, 2012
New nitrogen containing substituents at the indole-2-carboxamide yield high potent and broad spectrum indolylarylsulfone HIV-1 non-nucleoside reverse transcriptase inhibitors
Giuseppe La Regina, Antonio Coluccia, Andrea Brancale, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 39) with videos related to
Sort By:
Page
of 4
Journal of Medicinal Chemistry
|
May 11, 2012
Indole-2-carboxamides as allosteric modulators of the cannabinoid CB₁ receptor
Francesco Piscitelli, Alessia Ligresti, Giuseppe La Regina, et al.
The International Journal of Biochemistry & Cell Biology
|
April 22, 2009
Study of the effects of a new pyrazolecarboxamide: changes in mitochondria and induction of apoptosis
Vincenzo Giansanti, Tania Camboni, Francesco Piscitelli, et al.
Journal of Medicinal Chemistry
|
September 7, 2007
Indolyl aryl sulfones as HIV-1 non-nucleoside reverse transcriptase inhibitors: role of two halogen atoms at the indole ring in developing new analogues with improved antiviral activity
Giuseppe La Regina, Antonio Coluccia, Francesco Piscitelli, et al.
Journal of Medicinal Chemistry
|
March 4, 2011
Indolylarylsulfones as HIV-1 non-nucleoside reverse transcriptase inhibitors: new cyclic substituents at indole-2-carboxamide
Giuseppe La Regina, Antonio Coluccia, Andrea Brancale, et al.
Journal of Medicinal Chemistry
|
February 26, 2008
Synthesis, cannabinoid receptor affinity, and molecular modeling studies of substituted 1-aryl-5-(1H-pyrrol-1-yl)-1H-pyrazole-3-carboxamides
Romano Silvestri, Maria Grazia Cascio, Giuseppe La Regina, et al.
Journal of Medicinal Chemistry
|
April 16, 2010
Discovery of brain-penetrant, orally bioavailable aminothienopyridazine inhibitors of tau aggregation
Carlo Ballatore, Kurt R Brunden, Francesco Piscitelli, et al.
Bioorganic & Medicinal Chemistry
|
June 22, 2012
Aminothienopyridazine inhibitors of tau aggregation: evaluation of structure-activity relationship leads to selection of candidates with desirable in vivo properties
Carlo Ballatore, Alex Crowe, Francesco Piscitelli, et al.
Journal of Medicinal Chemistry
|
August 26, 2011
Cyclopentane-1,3-dione: a novel isostere for the carboxylic acid functional group. Application to the design of potent thromboxane (A2) receptor antagonists
Carlo Ballatore, James H Soper, Francesco Piscitelli, et al.
Journal of Medicinal Chemistry
|
May 26, 2006
Design, molecular modeling, synthesis, and anti-HIV-1 activity of new indolyl aryl sulfones. Novel derivatives of the indole-2-carboxamide
Rino Ragno, Antonio Coluccia, Giuseppe La Regina, et al.
Journal of Medicinal Chemistry
|
June 21, 2012
New nitrogen containing substituents at the indole-2-carboxamide yield high potent and broad spectrum indolylarylsulfone HIV-1 non-nucleoside reverse transcriptase inhibitors
Giuseppe La Regina, Antonio Coluccia, Andrea Brancale, et al.
Page
of 4