Zobrazeno 1 - 10
of 95
pro vyhledávání: '"L. Labeaga"'
Autor:
Martin K. Church, L. Labeaga
Publikováno v:
Journal of the European Academy of Dermatology and Venereology. 31:1447-1452
This review set out to examine published papers detailing the efficacy of bilastine in skin models and urticaria to assess whether it meets the optimal profile for updosing in urticaria, that is, strong clinical efficacy and freedom from unwanted sid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::259c19a759490d8b88321be237608127
https://doi.org/10.1111/jdv.14305
https://doi.org/10.1111/jdv.14305
Autor:
L. Labeaga, Sabine Altrichter, Tomasz Hawro, Torsten Zuberbier, Martin K. Church, Martin Metz, Markus Magerl, Marcus Maurer, Karsten Weller
Publikováno v:
Allergy. 73:2073-2075
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::211e37971f652926e564087f7ecf291c
https://doi.org/10.1111/all.13494
https://doi.org/10.1111/all.13494
Autor:
M K, Church, L, Labeaga
Publikováno v:
Journal of the European Academy of Dermatology and Venereology : JEADV. 31(9)
This review set out to examine published papers detailing the efficacy of bilastine in skin models and urticaria to assess whether it meets the optimal profile for updosing in urticaria, that is, strong clinical efficacy and freedom from unwanted sid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::60c7edd4ca9b4bf5d692676c0e87766e
https://pubmed.ncbi.nlm.nih.gov/28467671
https://pubmed.ncbi.nlm.nih.gov/28467671
Akademický článek
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Autor:
Juan Server-Carrió, Enrique Gálvez, A. Berisa, M. J. Fernandez, Antonio G. García, R. Huertas, L. Labeaga, Martín Martínez-Ripoll, A. Orjales, G. Uceda
Publikováno v:
Journal of Molecular Structure: THEOCHEM. 372:203-213
A series of amides derived from 3,7-dimethyl-3,7-diazabicyclo [3.3.1] nonan-9-amine have been synthesized and examined by 1 H and 13 C NMR spectroscopy and the crystal structure of 9-(2,4,6-trichlorobenzamido)-3,7-dimethyl-3,7-diazabicyclo[3.3.1] non
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::942a339ccebad73e24fc2d8005bf715c
https://doi.org/10.1016/s0166-1280(05)80013-2
https://doi.org/10.1016/s0166-1280(05)80013-2
Autor:
M.Martínez Ripoll, R. Huertas, A. Orjales, M. J. Fernandez, J. Server-Carrió, L. Labeaga, Enrique Gálvez, A. Berisa
Publikováno v:
Journal of Molecular Structure. 351:127-135
A series of esters derived from 3,7-dimethyl-3,7-diazabicyclo[3.3.1]nonan-9-ol has been synthesized and studied using 1H and 13C NMR spectroscopy and the crystal structure of 9-(3-indolycarbonyloxy)-3,7-dimethyl-3,7-diazabicyclo[3.3.1]nonane hydrochl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::959ba960270cd90bfee094275fba3151
https://doi.org/10.1016/0022-2860(94)08490-9
https://doi.org/10.1016/0022-2860(94)08490-9
Publikováno v:
Scopus-Elsevier
A series of N-phenethyl-8-β-amidocamphidines (4a-f) (3-phenethyl-8-β- (N-arylamido)-3-azabicyclo[3.2.1]octane) has been designed, synthesized and stereochemically characterized as semirigid analogous of the 4-ani- lidopiperidine analgesics in an at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1918f74d0ccb53b9b90d549102866439
https://doi.org/10.1002/jhet.5570310209
https://doi.org/10.1002/jhet.5570310209
Autor:
M. J. Fernandez, I. Fonseca, Aurelio Orjales, Armando Albert, Felix H. Cano, A. Berisa, Federico Gago, Jose Fayos, R. Huertas, L. Labeaga, Julia Sanz-Aparicio, Enrique Gálvez
Publikováno v:
ChemInform. 23
A series of 9-phenethyl-3-α-(N-arylamido)norgranatanes have been synthesized and studied by 1H and 13C-NMR spectroscopy, and the crystal structure of 9-phenethyl-3-α-(N-p-tolyl-p-chlorobenzamido)norgranatane has been determined by X-ray diffraction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7cad53c4f36101c9610921ae5474fd0
https://doi.org/10.1002/chin.199233196
https://doi.org/10.1002/chin.199233196
Publikováno v:
Drug design and discovery. 16(4)
A series of quinolinecarboxylic acid amides and an ester with a quinuclidine moiety were synthesized and their in vitro affinities at 5-HT3, 5-HT4, and D2 receptors evaluated by radioligand binding assays. Highest affinity at 5-HT3 receptor correspon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::df3509d5dfb97532d728173fc2849dd7
https://pubmed.ncbi.nlm.nih.gov/10807033
https://pubmed.ncbi.nlm.nih.gov/10807033
Autor:
A. Orjales, M.J Herranz, A. Berisa, Pedro Carmona, Isabel Iriepa, Juana Bellanato, B. Gil-Alberdi, Enrique Gálvez, L. Labeaga
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Digital.CSIC: Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
instname
Digital.CSIC: Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
A series of amides derived from 3-methyl-2,4-diphenyl-3-azabicyclo[3.3.1]nonan-9β-amine were synthesized and studied by IR, Raman, 1H and 13C NMR spectroscopy. The compounds studied displayed in CDCl3 a preferred flattened chair–chair conformation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4294a8ce53ef10c867344db3d2cd1ba
http://hdl.handle.net/10261/243735
http://hdl.handle.net/10261/243735
