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NOSCIRA SA

Overview
  • Total Patents
    103
About

NOSCIRA SA has a total of 103 patent applications. Its first patent ever was published in 2004. It filed its patents most often in EPO (European Patent Office), United States and Australia. Its main competitors in its focus markets pharmaceuticals, organic fine chemistry and measurement are PIMCO 2664 LTD, POTIER PIERRE and BIOLIPOX AB.

Patent filings per year

Chart showing NOSCIRA SAs patent filings per year from 1900 to 2020

Top inventors

# Name Total Patents
#1 Medina Padilla Miguel 62
#2 Martinez Gil Ana 47
#3 Castro Morera Ana 47
#4 Alonso Cascon Mercedes 36
#5 Garcia Palomero Esther 32
#6 Fuertes Huerta Ana 28
#7 Padilla Miguel Medina 27
#8 Gil Ana Martinez 27
#9 Usan Egea Paola 24
#10 Lopez Ogalla Javier 23

Latest patents

Publication Filing date Title
EP2662081A1 Therapeutic use of indole-dihydro-imidazole derivatives
EP2647634A1 Indole-pyrimidine derivatives and their therapeutic uses
WO2012069428A1 Bipyridine sulfonamide derivatives for the treatment of neurodegenerative diseases or conditions
WO2011151359A1 Combined treatment with a cholinesterase inhibitor and a thiadiazolidinedione derivative
EP2527323A1 Urea carbonyl disulfide derivatives and their therapeutic uses
EP2527322A1 Carbamyl alkylphenyl disulfide derivatives and their therapeutic uses
EP2281824A1 Furan-imidazolone derivatives, for the treatment of cognitive, neurodegenerative or neuronal diseases or disorders
CN101952234A Phenyl-prenyl derivatives, of marine and synthetic origin, for the treatment of cognitive, neurodegenerative or neuronal diseases or disorders
EP2196466A1 Triple substituted phenanthroline derivatives for the treatment of neurodegenerative or heamatological diseases or conditions
MX2009001171A N-phenyl-prenylamine derivatives for the treatment of cognitive, neurodegenerative or neuronal diseases or disorders.
EP2002863A1 [1,10]-phenanthroline derivatives for the treatment of neurodegenerative or haematological diseases
ZA200809951B N-(2-Thiazolyl)-amide derivatives as GSK-3 inhibitors