Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Montserrat Heras"'
Autor:
Rita F. Belo, Margarida L. F. Martins, Liana Shvachiy, Tiago Costa-Coelho, Carolina de Almeida-Borlido, João Fonseca-Gomes, Vera Neves, Hugo Vicente Miranda, Tiago F. Outeiro, Joana E. Coelho, Sara Xapelli, Cláudia A. Valente, Montserrat Heras, Eduard Bardaji, Miguel A. R. B. Castanho, Maria José Diógenes, Ana M. Sebastião
Publikováno v:
Frontiers in Pharmacology, Vol 11 (2020)
Kyotorphin (KTP, l-tyrosyl-l-arginine) is an endogenous dipeptide initially described to have analgesic properties. Recently, KTP was suggested to be an endogenous neuroprotective agent, namely for Alzheimer’s disease (AD). In fact, KTP levels were
Externí odkaz:
https://doaj.org/article/23add04407fb425ba6cdc74be1ceea14
Autor:
Eva Marguí, Maria Lluisa Escoda, Montserrat Heras, Mònica Iglesias, Maria Dolors Verdaguer, David Pavón, Marcel Vergés
Publikováno v:
INTED2023 Proceedings.
Autor:
Vasanthakumar G. Ramu, Montserrat Heras, Eduard Bardají, Jéssica Diane dos Santos, Miguel A. R. B. Castanho, Katia Conceição, Juliana Campos Junqueira, Vitor Martins de Andrade
Publikováno v:
Web of Science
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
© 2019 British Mycological Society. Published by Elsevier Ltd. All rights reserved.
Kyotorphin (KTP, l-tyrosyl-l-arginine) is an endogenous analgesic neuropeptide first isolated from bovine brain in 1979. Previous studies have shown that kyotor
Kyotorphin (KTP, l-tyrosyl-l-arginine) is an endogenous analgesic neuropeptide first isolated from bovine brain in 1979. Previous studies have shown that kyotor
Autor:
Maria Cristina Oliveira, Isa Serrano, Miguel A. R. B. Castanho, Isabel Santos, Juliana Perazzo, Sónia Sá Santos, João D. G. Correia, Isaura Tavares, Eduard Bardají, Marta M. B. Ribeiro, Montserrat Heras, Lurdes Gano
Publikováno v:
MedChemComm. 7:906-913
Amidated kyotorphin (L-Tyr-L-Arg-NH2; KTP-NH2) shows analgesic properties following systemic administration. Although KTP-NH2 does not have toxic effects in the liver, its biodistribution is unknown. KTP-NH2 was radioiodinated to evaluate its biologi
Autor:
Montserrat Heras, Abdelatif ElMarrouni
Publikováno v:
© Organic and Biomolecular Chemistry, 2015, vol. 13, núm. 3, p. 851-858
Articles publicats (D-Q)
DUGiDocs – Universitat de Girona
instname
Articles publicats (D-Q)
DUGiDocs – Universitat de Girona
instname
The p-benzyloxybenzyloxy group is used to mask the oxo function of the 4(3H)-pyrimidinone ring in the synthesis of new unnatural amino acids. The synthetic approach is based on an aromatic nucleophilic substitution reaction between 4-[4-(benzyloxy)be
Autor:
Isaura Tavares, João M. Freire, Montserrat Heras, Vasanthakumar G. Ramu, Miguel A. R. B. Castanho, Antónia R. T. Pinto, Isa Serrano, Eduard Bardají
Publikováno v:
Biopolymers. 104:1-10
Amidated kyotorphin (l-Tyr-l-Arg-NH2; KTP-NH2) causes analgesia when systemically administered. The lipophilic ibuprofen-conjugated derivative of KTP-NH2 has improved analgesic efficacy. However, fast degradation by peptidases impacts negatively in t
Autor:
Miguel A. R. B. Castanho, Juliana Perazzo, Montserrat Heras, Mônica Lopes-Ferreira, Carla Lima, Eduard Bardají
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
ACS Chemical Neuroscience
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
ACS Chemical Neuroscience
© 2017 American Chemical Society
Neuropeptide kyotorphin (KTP) is a potent analgesic if administered directly into the brain. In contrast, KTP-amide (KTP-NH2) is analgesic, neuroprotective, and anti-inflammatory following systemic administratio
Neuropeptide kyotorphin (KTP) is a potent analgesic if administered directly into the brain. In contrast, KTP-amide (KTP-NH2) is analgesic, neuroprotective, and anti-inflammatory following systemic administratio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a0bf0b6c8442d9b48e00b40440f91e7
https://hdl.handle.net/10451/32603
https://hdl.handle.net/10451/32603
Quantitative analysis of molecular partition towards lipid membranes using surface plasmon resonance
Autor:
Catarina Cunha-Santos, Montserrat Heras, Ana Salomé Veiga, Matteo Porotto, João M. Freire, João Gonçalves, Tiago N. Figueira, Anne Moscona, Miguel A. R. B. Castanho
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
instname
Scientific Reports
Scientific Reports, Nature Publishing Group, 2017, 7, pp.45647. ⟨10.1038/srep45647⟩
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Scientific Reports, 2017, vol.7, art. núm. 45647
Articles publicats (D-Q)
DUGiDocs – Universitat de Girona
Scientific Reports, 2017, 7, pp.45647. ⟨10.1038/srep45647⟩
instname
Scientific Reports
Scientific Reports, Nature Publishing Group, 2017, 7, pp.45647. ⟨10.1038/srep45647⟩
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Scientific Reports, 2017, vol.7, art. núm. 45647
Articles publicats (D-Q)
DUGiDocs – Universitat de Girona
Scientific Reports, 2017, 7, pp.45647. ⟨10.1038/srep45647⟩
© The Author(s) 2017. This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3978fed9394ac2a64dcd8d6b31116457
https://hdl.handle.net/10451/32602
https://hdl.handle.net/10451/32602
Publikováno v:
Synthesis. 46:1481-1486
The synthesis of IbKTP-NH2 with reduction of racemization up to no detectable level has been achieved using 3-(diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-one (DEPBT). Among all coupling systems tested, only DEPBT-mediated amide bond formation be
Autor:
Isa Serrano, Carla Lima, Miguel A. R. B. Castanho, Eduard Bardají, Isaura Tavares, Mônica Lopes-Ferreira, Montserrat Heras, Sónia Sá Santos, Juliana Perazzo, Antónia R. T. Pinto, Katia Conceição
Publikováno v:
ACS Chemical Neuroscience
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
© 2016 American Chemical Society
Kyotorphin (KTP) is an endogenous peptide with analgesic properties when administered into the central nervous system (CNS). Its amidated form (l-Tyr-l-Arg-NH2; KTP-NH2) has improved analgesic efficacy after sys
Kyotorphin (KTP) is an endogenous peptide with analgesic properties when administered into the central nervous system (CNS). Its amidated form (l-Tyr-l-Arg-NH2; KTP-NH2) has improved analgesic efficacy after sys