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giovanna.poce@uniroma1.it
Giovanna Poce
Professore Associato
Struttura:
DIPARTIMENTO DI CHIMICA E TECNOLOGIE DEL FARMACO
E-mail:
giovanna.poce@uniroma1.it
Pagina istituzionale corsi di laurea
Curriculum Sapienza
Pubblicazioni
Titolo
Pubblicato in
Anno
Chocolate consumers and lymphocyte-to-monocyte ratio: a working hypothesis from a preliminary report of a pilot study in celiac subjects
ANTIOXIDANTS
2019
Development of MmpL3 inhibitors for tuberculosis treatment
Medicinal Chemistry approaches to tuberculosis and trypanosomiasis
2019
In vivo potent BM635 analogue with improved drug-like properties
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
2018
Stimuli-responsive tannin–feIII hybrid microcapsules demonstrated by the active release of an anti-tuberculosis agent
CHEMSUSCHEM
2018
1,5-Diarylpyrroles as potent antitubercular and anti-inflammatory agents
CHEMISTRY OF HETEROCYCLIC COMPOUNDS
2017
MmpL3 is the flippase for mycolic acids in mycobacteria
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
2017
Pharmaceutical salt of BM635 with improved bioavailability
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES
2017
Synthesis and biological evaluation of fluorinated 1,5-diarylpyrrole-3-alkoxyethyl ether derivatives as selective COX-2 inhibitors endowed with anti-inflammatory activity
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
2016
A series of COX-2 inhibitors endowed with NO-releasing properties: synthesis, biological evaluation, and docking analysis
CHEMMEDCHEM
2016
MmpL3 inhibitors: diverse chemical scaffolds inhibit the same target
MINI-REVIEWS IN MEDICINAL CHEMISTRY
2016
A novel antimycobacterial compound acts as an intracellular iron chelator
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
2015
Activity of lipophilic and hydrophilic drugs against dormant and replicating mycobacterium tuberculosis
JOURNAL OF ANTIBIOTICS
2015
COX inhibitors: a patent review (2011 - 2014)
EXPERT OPINION ON THERAPEUTIC PATENTS
2015
Overcoming drug resistance for tuberculosis
FUTURE MICROBIOLOGY
2015
Synthesis, biological evaluation and docking analysis of a new series of methylsulfonyl and sulfamoyl acetamides and ethyl acetates as potent COX-2 inhibitors
BIOORGANIC & MEDICINAL CHEMISTRY
2015
Synthesis, biological evaluation and docking analysis of a new series of methylsulfonyl and sulfamoyl acetamides and ethyl acetates as potent COX-2 inhibitors
BIOORGANIC & MEDICINAL CHEMISTRY
2015
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Progetti di Ricerca
Nuovi derivati pirazolici come potenziali agenti anti-tubercolari
Nuovi derivati tri-antranilati come potenziali agenti anti-tubercolari
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