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Manel Ferrer
Institutions:
Centro de Investigación y Desarrollo,
Almirall (Spain)
Observed institutions:
Centro de Investigación y Desarrollo,
Almirall (Spain)
OpenAlex ID:
A5045445557
Biphenyl Pyridazinone Derivatives as Inhaled PDE4 Inhibitors: Structural Biology and Structure–Activity Relationships
2016
·
Jordi Gràcia
, Maria Antonia Buil
, et al.
·
Journal of Medicinal Chemistry
·
29
Structure-activity relationships (SAR) and structure-kinetic relationships (SKR) of sulphone-based CRTh2 antagonists
2016
·
Maria Antonia Buil
, Marta Calbet
, et al.
·
European Journal of Medicinal Chemistry
·
20
4-Amino-7,8-dihydro-1,6-naphthyridin-5(6H)-ones as Inhaled Phosphodiesterase Type 4 (PDE4) Inhibitors: Structural Biology and Structure–Activity Relationships
2018
·
Richard S. Roberts
, Sara Sevilla
, et al.
·
Journal of Medicinal Chemistry
·
19
Structure–activity relationships (SAR) and structure–kinetic relationships (SKR) of pyrrolopiperidinone acetic acids as CRTh2 antagonists
2014
·
Miriam Andrés
, Maria Antonia Buil
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
19
Solid-phase syntheses of N-substituted carbamates. Reaction monitoring by gel-phase 13C NMR using a 13C enriched BAL-linker
2002
·
Dolors Fernández-Forner
, Josep M Huerta
, et al.
·
Tetrahedron Letters
·
15
2-(1H-Pyrazol-4-yl)acetic acids as CRTh2 antagonists
2013
·
Miriam Andrés
, Mónica Bravo
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
13
2-(1H-Pyrazol-1-yl)acetic acids as chemoattractant receptor-homologous molecule expressed on Th2 lymphocytes (CRTh2) antagonists
2014
·
Miriam Andrés
, Mónica Bravo
, et al.
·
European Journal of Medicinal Chemistry
·
12
Structure–activity relationships (SAR) and structure–kinetic relationships (SKR) of bicyclic heteroaromatic acetic acids as potent CRTh2 antagonists III: The role of a hydrogen-bond acceptor in long receptor residence times
2014
·
Juan Antonio Alonso
, Miriam Andrés
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
10
A modular synthesis of novel 4-amino-7,8-dihydro-1,6-naphthyridin-5(6H)-ones as PDE4 inhibitors
2013
·
Manel Ferrer
, Richard S. Roberts
, et al.
·
Tetrahedron Letters
·
8
Structure–activity relationships (SAR) and structure–kinetic relationships (SKR) of bicyclic heteroaromatic acetic acids as potent CRTh2 antagonists II: Lead optimization
2014
·
Juan Antonio Alonso
, Miriam Andrés
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
5
ChemInform Abstract: A Modular Synthesis of Novel 4‐Amino‐7,8‐dihydro‐1,6‐naphthyridin‐5‐(6H)‐ones as PDE4 Inhibitors.
2013
·
Manel Ferrer
, Richard S. Roberts
, et al.
·
ChemInform
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Works count:
11
Citation count:
150
H-index:
8
I10-index:
8
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