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CORDIS - Risultati della ricerca dell’UE
CORDIS

Selective Agonists For Serotonin Receptors

Risultati finali

Functionally selective ligand scaffolds from virtual screening

Virtual screening for new 5HT2A ligand scaffolds with functional selectivity

Holistic signalling pathway profiles of new 5-HT2A ligands

Evaluate the receptor subtype and signalling pathwayprofiles of new inhouse lead ligands from synthesis T23 and VS T24

2nd report on dissemination activities

Report on dissemination/outreach activities

3rd report on dissemination activities

Report on dissemination/outreach activities

Functionally selective ligands from in-house synthesis

Synthesise putatively modelbased selective ligands

Model of structural mechanisms for 5-HT2A biased agonism

Build 3D molecular models for rationalisation and design of functionally selective 5HT2A ligands

1st report on dissemination activities

Report on dissemination/outreach activities

4th report on dissemination activities

Report on dissemination/outreach activities

Ligand database incl. biased agonism – public version in GPCRdb

Provide data design specifications and inhouse pilot data

SAFER web site

SAFER website implementation.

Pubblicazioni

GPCRdb in 2021: integrating GPCR sequence, structure and function

Autori: Albert J Kooistra, Stefan Mordalski, Gáspár Pándy-Szekeres, Mauricio Esguerra, Alibek Mamyrbekov, Christian Munk, György M Keserű, David E Gloriam
Pubblicato in: Nucleic Acids Research, Numero 49/D1, 2020, Pagina/e D335-D343, ISSN 0305-1048
Editore: Oxford University Press
DOI: 10.1093/nar/gkaa1080

Structural insights into the lipid and ligand regulation of serotonin receptors

Autori: Peiyu Xu, Sijie Huang, Huibing Zhang, Chunyou Mao, X. Edward Zhou, Xi Cheng, Icaro A. Simon, Dan-Dan Shen, Hsin-Yung Yen, Carol V. Robinson, Kasper Harpsøe, Bo Svensson, Jia Guo, Hualiang Jiang, David E. Gloriam, Karsten Melcher, Yi Jiang, Yan Zhang, H. Eric Xu
Pubblicato in: Nature, Numero 592/7854, 2021, Pagina/e 469-473, ISSN 0028-0836
Editore: Nature Publishing Group
DOI: 10.1038/s41586-021-03376-8

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