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Caterina Musetti

Showing results (11-20 of 18) with videos related to

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Journal of Medicinal Chemistry|January 9, 2013
Identification and characterization of new DNA G-quadruplex binders selected by a combination of ligand and structure-based virtual screening approachesStefano Alcaro, Caterina Musetti, Simona Distinto, et al.
Current Pharmaceutical Design|March 3, 2012
Heterocyclic dications as a new class of telomeric G-quadruplex targeting agentsRupesh Nanjunda, Caterina Musetti, Arvind Kumar, et al.
Oncotarget|March 5, 2016
Screening of candidate G-quadruplex ligands for the human c-KIT promotorial region and their effects in multiple in-vitro modelsEleonora Zorzan, Silvia Da Ros, Caterina Musetti, et al.
European Journal of Medicinal Chemistry|July 24, 2012
Structure-activity relationships of novel substituted naphthalene diimides as anticancer agentsAndrea Milelli, Vincenzo Tumiatti, Marialuisa Micco, et al.
Nature|January 21, 2026
Identification of an allosteric site on the E3 ligase adapter cereblonVanessa N Dippon, Zeba Rizvi, Anthony E Choudhry, et al.
Bioorganic & Medicinal Chemistry Letters|May 15, 2021
A knowledge-based, structural-aided discovery of a novel class of 2-phenylimidazo[1,2-a]pyridine-6-carboxamide H-PGDS inhibitorsChristie A Schulte, David N Deaton, Elsie Diaz, et al.
Bioorganic & Medicinal Chemistry|October 15, 2020
The exploration of aza-quinolines as hematopoietic prostaglandin D synthase (H-PGDS) inhibitors with low brain exposureRodolfo Cadilla, David N Deaton, Young Do, et al.
Bioorganic & Medicinal Chemistry|March 13, 2019
The discovery of quinoline-3-carboxamides as hematopoietic prostaglandin D synthase (H-PGDS) inhibitorsDavid N Deaton, Young Do, Jason Holt, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Journal of Medicinal Chemistry|January 9, 2013
Identification and characterization of new DNA G-quadruplex binders selected by a combination of ligand and structure-based virtual screening approachesStefano Alcaro, Caterina Musetti, Simona Distinto, et al.
Current Pharmaceutical Design|March 3, 2012
Heterocyclic dications as a new class of telomeric G-quadruplex targeting agentsRupesh Nanjunda, Caterina Musetti, Arvind Kumar, et al.
Oncotarget|March 5, 2016
Screening of candidate G-quadruplex ligands for the human c-KIT promotorial region and their effects in multiple in-vitro modelsEleonora Zorzan, Silvia Da Ros, Caterina Musetti, et al.
European Journal of Medicinal Chemistry|July 24, 2012
Structure-activity relationships of novel substituted naphthalene diimides as anticancer agentsAndrea Milelli, Vincenzo Tumiatti, Marialuisa Micco, et al.
Nature|January 21, 2026
Identification of an allosteric site on the E3 ligase adapter cereblonVanessa N Dippon, Zeba Rizvi, Anthony E Choudhry, et al.
Bioorganic & Medicinal Chemistry Letters|May 15, 2021
A knowledge-based, structural-aided discovery of a novel class of 2-phenylimidazo[1,2-a]pyridine-6-carboxamide H-PGDS inhibitorsChristie A Schulte, David N Deaton, Elsie Diaz, et al.
Bioorganic & Medicinal Chemistry|October 15, 2020
The exploration of aza-quinolines as hematopoietic prostaglandin D synthase (H-PGDS) inhibitors with low brain exposureRodolfo Cadilla, David N Deaton, Young Do, et al.
Bioorganic & Medicinal Chemistry|March 13, 2019
The discovery of quinoline-3-carboxamides as hematopoietic prostaglandin D synthase (H-PGDS) inhibitorsDavid N Deaton, Young Do, Jason Holt, et al.
Pageof 2