Abstract: The present invention relates to an antibacterial peptide having from the amino to the carboxylic terminal an amino acid sequences selected from the group of: KKIRVRLSA, SEQ ID NO. 1, RRIRVRLSA, SEQ ID NO. 2, KRIRVRLSA, SEQ ID NO. 3, RKIRVRLSA, SEQ ID NO. 4 or a derivative thereof and uses thereof.
Abstract: The present invention concerns a peptide having anti-tumour activity and its related pharmaceutical compositions. In particular, the invention concerns a peptide with anti-tumour preventive and therapeutic activity, also in combination with other known anti-tumour compounds such as, for example, 5-fluorouracil.
Type:
Grant
Filed:
February 15, 2006
Date of Patent:
January 1, 2013
Assignee:
Universitá degli Studi di Siena
Inventors:
Pierpaolo Correale, Maria Grazia Cusi, Guido Francini, Giorgio Giorgi
Abstract: Antibacterial peptides and their multimeric analogues, with a wide range of action and low haemolytic activity are described. In particular, the peptide molecules exhibit a high antimicrobial activity against numerous bacterial species, with reduced cytotoxicity and a low haemolysis rate. The molecules of the invention are advantageously usable as therapeutic agents and coadjutants against infections caused by strains that are resistant to common antibiotics.
Type:
Grant
Filed:
July 13, 2005
Date of Patent:
September 18, 2012
Assignee:
Universita Degli Studi di Siena
Inventors:
Luisa Bracci, Andrea Giuliani, Alessandro Pini, Paolo Neri
Abstract: Antigenic protein fragments of Streptococcus pneumoniae to be used for the preparation of a medicament for the prevention and the treatment of bacterial infections and a method for the detection thereof, and related compositions using said epitopes, are disclosed.
Abstract: The present invention relates to an antibacterial peptide having from the amino to the carboxylic terminal an amino acid sequences selected from the group of: KKIRVRLSA, SEQ ID NO. 1, RRIRVRLSA, SEQ ID NO. 2, KRIRVRLSA, SEQ ID NO. 3, RKIRVRLSA, SEQ ID NO. 4 or a derivative thereof and uses thereof.
Abstract: The present invention is directed to the use of the expression level of the pro-EPIL gene as a biomarker for the diagnosing of testicular cancer, particularly a testicular germ cell tumor. The invention also relates to an in vitro method for detecting and/or classifying a testicular cancer in a subject comprising a step of determining the expression level of the gene encoding the pro-EPIL peptide in a biological, particularly in combination with the determination of the beta subunit HCG? and the human alpha-fetoprotein AFP. The invention is also directed to a kit or solid support comprising nucleic acids or antibodies capable of determining the presence or the expression level of these three biological markers.
Type:
Application
Filed:
April 28, 2009
Publication date:
May 5, 2011
Applicants:
Universite Paris Descartes, Centre National De La Recherche Scientifique (CNRS), Universita Degli Studi Di Siena, Institut Curie (formerly Centre Rene Huguenin), Institut Gustave Roussy
Inventors:
Dominique Bellet, Alain Pecking, Sophie Richon, Felice Petraglia
Abstract: The present invention relates to linear and cyclic guanidine derivatives, method of preparation and uses thereof, pharmaceutical compositions to be used as antifungal agents, in particular against Candida species.
Type:
Application
Filed:
March 12, 2009
Publication date:
February 17, 2011
Applicant:
UNIVERSITÀ DEGLI STUDI DI SIENA
Inventors:
Maurizio Botta, Francesco Raffi, Paolo Visca
Abstract: The present invention relates to a compound 4-substituted derivative of pyrazolo[3,4-d]pyrimidine or of pyrrolo[2,3-d]pyrimidine having the formula (I) and uses thereof, in particular for the treatment of bone related diseases and tumours.
Type:
Application
Filed:
September 12, 2008
Publication date:
September 30, 2010
Applicant:
UNIVERSITA DEGLI STUDI DI SIENA
Inventors:
Silvia Schenone, Francesco Bondavalli, Olga Bruno, Maurizio Botta, Fabrizio Manetti, Marco Radi, Alessandra Santucci, Giovanni Maga, Mauro Bologna, Adriano Angelucci, Annalisa Santucci, Adriano Spreafico, Fabio Carraro, Jurgen Borlak
Abstract: Soluble pharmaceutical composition for the treatment of articular pathologies comprising an effective amount of a least one linear or cyclic polymetaphosphate or a soluble and pharmaceutically acceptable salt thereof, and appropriate diluents.
Abstract: This invention provides novel aryl piperazine derivatives represented by Formula (I) having medical utility, in particular as modulators of dopamine and serotonin receptors, preferably the D3, 5HT1A and 5-HT2A receptor subtypes, and in particular useful for the treatment of neuropsychiatric disorders, incl. schizophrenia.
Type:
Application
Filed:
October 12, 2007
Publication date:
April 8, 2010
Applicant:
Universita degli Studi di Siena
Inventors:
Giuseppe Campiani, Stefania Butini, Caterina Fattorusso, Silvia Franceschini, Irene Zia Thale, Karin Sandager Nielsen, Jørgen Scheel-Krüeger, Lars Siim Madsen
Abstract: This invention provides novel aryl piperazine derivatives having medical utility, in particular as modulators of dopamine and serotonin receptors, preferably the D3, D2-like and 5-HT2 receptor subtypes, and in particular useful for the treatment of neuropsychiatric disorders incl. schizophrenia.
Type:
Application
Filed:
January 2, 2006
Publication date:
September 24, 2009
Applicant:
Universita Degli Studi Di Siena
Inventors:
Giuseppe Campiani, Stefania Butini, Caterina Fattorusso, Francesco Trotta, Silvia Franceschini, Meri De Angelis, Karin Sandager Nielsen
Abstract: The present invention provides a compound of pyrazolo[3,4-d]pyrimidine having the formula wherein: X=N; R=H, alkylthio, or aminoalkylthio; R1=NHcyclopropyl, NHC3H7, NHC4H9, N(CH2CH3)2, NHCH2CH2OC2H5, 1-pyrrolidinyl, 1-piperidinyl, 4-morpholinyl, NHcyclohexyl, 1-hexahydroazepinyl, NHCH2C6H5, or NHCH2CH2C6H5; wherein R3=H, halogen, or alkyl and R5=Cl, Br or OH.
Type:
Grant
Filed:
May 26, 2004
Date of Patent:
September 15, 2009
Assignee:
Universita degli Studi di Siena
Inventors:
Francesco Bondavalli, Maurizio Botta, Olga Bruno, Fabrizio Manetti, Silvia Schenone, Fabio Carraro
Abstract: The present invention concerns an automatic method for measuring a baby's cry, comprising the following step: A. having N samples ?(i), for i=O, 1, . . . , (N?1), of an acoustic signal p(t) representing the cry, sampled at a sampling frequency? for a period of duration P; the method being characterised in that it assigns a score PainScore to the acoustic signal p(t) by means of a function AF of one or more acoustic parameters selected from the group comprising: —a root-mean-square or rms value prms of the acoustic signal p(t) in the period P; —a fundamental or pitch frequency F0 of the acoustic signal p(t), i.e. the minimum frequency at which a peak in the spectrum of the acoustic signal p(t) occurs in the period P; and—a configuration of amplitude and frequency modulation of the acoustic signal p(t) in the period P. The invention further concerns the apparatus performing the method.
Type:
Application
Filed:
March 10, 2006
Publication date:
September 25, 2008
Applicants:
UNIVERSITA' DEGLI STUDI DI SIENA, AZIENDA OSPEDALIERA UNIVERSITARIA SENESE
Inventors:
Renata Sisto, Carlo Valerio Bellieni, Giuseppe Buonocore
Abstract: A nucleic acid comprising at least one fragment of the human FACL4 gene or FACL4 protein or functional portions thereof for diagnostic or therapeutic purposes applied to syndromes associated with mental retardation is described. Appropriate diagnostic kits are also described.