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Molecules (Basel, Switzerland)
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July 27, 2010
Synthesis and biological evaluation of a gamma-cyclodextrin-based formulation of the anticancer agent 5,6,11,12,17,18,23,24-octahydrocyclododeca[1,2-b:4,5-b':7,8-b'':10,11-b''']tetraindole (CTet)
Simone Lucarini, Mauro De Santi, Francesca Antonietti, et al.
Chemmedchem
|
August 29, 2012
MT1-selective melatonin receptor ligands: synthesis, pharmacological evaluation, and molecular dynamics investigation of N-{[(3-O-substituted)anilino]alkyl}amides
Silvia Rivara, Daniele Pala, Alessio Lodola, et al.
Anti-Cancer Agents in Medicinal Chemistry
|
October 25, 2012
Antitumoral activity of indole-3-carbinol cyclic tri- and tetrameric derivatives mixture in human breast cancer cells: in vitro and in vivo studies
Giorgio Brandi, Alessandra Fraternale, Simone Lucarini, et al.
Pharmaceutics
|
July 5, 2018
Synthesis, Structure⁻Activity Relationships and In Vitro Toxicity Profile of Lactose-Based Fatty Acid Monoesters as Possible Drug Permeability Enhancers
Simone Lucarini, Laura Fagioli, Robert Cavanagh, et al.
Journal of Medicinal Chemistry
|
December 8, 2006
Design and synthesis of N-(3,3-diphenylpropenyl)alkanamides as a novel class of high-affinity MT2-selective melatonin receptor ligands
Annalida Bedini, Gilberto Spadoni, Giuseppe Gatti, et al.
Colloids and Surfaces. B, Biointerfaces
|
November 2, 2023
The influence of mannose-based esters on the mesophase behaviour of lyotropic liquid crystalline nanosystems as drug delivery vectors
Mattia Tiboni, Paola Astolfi, Michele Verboni, et al.
ACS Omega
|
January 5, 2022
Phenotype Screening of an Azole-bisindole Chemical Library Identifies URB1483 as a New Antileishmanial Agent Devoid of Toxicity on Human Cells
Aurora Diotallevi, Laura Scalvini, Gloria Buffi, et al.
Journal of Medicinal Chemistry
|
November 4, 2011
Toward the definition of stereochemical requirements for MT2-selective antagonists and partial agonists by studying 4-phenyl-2-propionamidotetralin derivatives
Annalida Bedini, Simone Lucarini, Gilberto Spadoni, et al.
Breast Cancer Research : BCR
|
March 26, 2011
The indole-3-carbinol cyclic tetrameric derivative CTet inhibits cell proliferation via overexpression of p21/CDKN1A in both estrogen receptor-positive and triple-negative breast cancer cell lines
Mauro De Santi, Luca Galluzzi, Simone Lucarini, et al.
Plos One
|
June 13, 2024
Exploring hydrophilic 2,2-di(indol-3-yl)ethanamine derivatives against Leishmania infantum
Alessia Centanni, Aurora Diotallevi, Gloria Buffi, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 58) with videos related to
Sort By:
Page
of 6
Molecules (Basel, Switzerland)
|
July 27, 2010
Synthesis and biological evaluation of a gamma-cyclodextrin-based formulation of the anticancer agent 5,6,11,12,17,18,23,24-octahydrocyclododeca[1,2-b:4,5-b':7,8-b'':10,11-b''']tetraindole (CTet)
Simone Lucarini, Mauro De Santi, Francesca Antonietti, et al.
Chemmedchem
|
August 29, 2012
MT1-selective melatonin receptor ligands: synthesis, pharmacological evaluation, and molecular dynamics investigation of N-{[(3-O-substituted)anilino]alkyl}amides
Silvia Rivara, Daniele Pala, Alessio Lodola, et al.
Anti-Cancer Agents in Medicinal Chemistry
|
October 25, 2012
Antitumoral activity of indole-3-carbinol cyclic tri- and tetrameric derivatives mixture in human breast cancer cells: in vitro and in vivo studies
Giorgio Brandi, Alessandra Fraternale, Simone Lucarini, et al.
Pharmaceutics
|
July 5, 2018
Synthesis, Structure⁻Activity Relationships and In Vitro Toxicity Profile of Lactose-Based Fatty Acid Monoesters as Possible Drug Permeability Enhancers
Simone Lucarini, Laura Fagioli, Robert Cavanagh, et al.
Journal of Medicinal Chemistry
|
December 8, 2006
Design and synthesis of N-(3,3-diphenylpropenyl)alkanamides as a novel class of high-affinity MT2-selective melatonin receptor ligands
Annalida Bedini, Gilberto Spadoni, Giuseppe Gatti, et al.
Colloids and Surfaces. B, Biointerfaces
|
November 2, 2023
The influence of mannose-based esters on the mesophase behaviour of lyotropic liquid crystalline nanosystems as drug delivery vectors
Mattia Tiboni, Paola Astolfi, Michele Verboni, et al.
ACS Omega
|
January 5, 2022
Phenotype Screening of an Azole-bisindole Chemical Library Identifies URB1483 as a New Antileishmanial Agent Devoid of Toxicity on Human Cells
Aurora Diotallevi, Laura Scalvini, Gloria Buffi, et al.
Journal of Medicinal Chemistry
|
November 4, 2011
Toward the definition of stereochemical requirements for MT2-selective antagonists and partial agonists by studying 4-phenyl-2-propionamidotetralin derivatives
Annalida Bedini, Simone Lucarini, Gilberto Spadoni, et al.
Breast Cancer Research : BCR
|
March 26, 2011
The indole-3-carbinol cyclic tetrameric derivative CTet inhibits cell proliferation via overexpression of p21/CDKN1A in both estrogen receptor-positive and triple-negative breast cancer cell lines
Mauro De Santi, Luca Galluzzi, Simone Lucarini, et al.
Plos One
|
June 13, 2024
Exploring hydrophilic 2,2-di(indol-3-yl)ethanamine derivatives against Leishmania infantum
Alessia Centanni, Aurora Diotallevi, Gloria Buffi, et al.
Page
of 6